Background: Although endometrial cancer is clearly influenced by hormonal factors, few epidemiologic studies have investigated the role of endogenous estrogens or especially estrogen metabolites.

Methods: We conducted a nested case–control study within the Women's Health Initiative Observational Study (WHI-OS), a cohort of 93,676 postmenopausal women recruited between 1993 and 1998. Using baseline serum samples from women who were non-current hormone users with intact uteri, we measured 15 estrogens/estrogen metabolites via HPLC/MS-MS among 313 incident endometrial cancer cases (271 type I, 42 type II) and 354 matched controls, deriving adjusted ORs and 95% confidence intervals (CI) for overall and subtype-specific endometrial cancer risk.

Results: Parent estrogens (estrone and estradiol) were positively related to endometrial cancer risk, with the highest risk observed for unconjugated estradiol (OR 5th vs. 1st quintile = 6.19; 95% CI, 2.95–13.03, Ptrend = 0.0001). Nearly all metabolites were significantly associated with elevated risks, with some attenuation after adjustment for unconjugated estradiol (residual risks of 2- to 3-fold). Body mass index (kg/m2, BMI) relations were somewhat reduced after adjustment for estrogen levels. The association with unconjugated estradiol was stronger for type I than type II tumors (Phet = 0.01).

Conclusions: Parent estrogens as well as individual metabolites appeared to exert generalized uterotropic activity, particularly for type I tumors. The effects of obesity on risk were only partially explained by estrogens.

Impact: These findings enhance our understanding of estrogen mechanisms involved in endometrial carcinogenesis but also highlight the need for studying additional markers that may underlie the effects on risk of certain risk factors, for example, obesity. Cancer Epidemiol Biomarkers Prev; 25(7); 1081–9. ©2016 AACR.

Endometrial cancer is strongly influenced by hormonal factors, with established risk factors including obesity, menstrual and reproductive factors, and exogenous hormones (1). Despite acceptance of the hormonal etiology of endometrial cancer, relatively few studies have explored the role of endogenous estrogens (2). Although several epidemiologic investigations have shown strong associations with risk (3–6), results have generally been based on limited numbers of cases (e.g., 57–124 cases were involved with two of the studies). In addition, previous investigations have mainly relied on measurement of estrogens by radioimmunoassays, which have recognized limitations, particularly for measuring low concentrations of estrogens in postmenopausal women.

The use of mass spectrometry to measure endogenous hormones has opened up new research avenues (7). In addition to improving sensitivity, accuracy, and reproducibililty, these assays have enabled concurrent measurement of estrogen metabolites, which purportedly have divergent effects on cancer development. The metabolism of estradiol or estrone with irreversible hydroxylation at the C-2, C-4, or C-16 positions of the steroid ring results in metabolites with varying mitogenic and genotoxic properties. Two major hypotheses about estrogen metabolites have emerged from experimental research, namely, that (i) 16α-hydroxyestrone (16α-OHE1) is carcinogenic because it can bind covalently to the estrogen receptor with strong mitogenic effects, and (ii) the 2- and 4-hydroxylation catechol estrogen metabolites are carcinogenic because they can be oxidized into mutagenic quinones that form DNA adducts and lead to oxidative DNA damage (7).

Estrogen metabolites have been most extensively evaluated with respect to breast cancer, where initial attention focused on potential mitogenic effects, with the hypotheses that high levels of 16α-OHE1 would be directly associated with risk, whereas high ratios of 2-hydroxyestrone (2-OHE1) to 16α-OHE1 would be inversely related (8, 9). More recent studies have focused on genotoxicity (10), given that hydroxylation at the C-2 and C-4 positions produces catechol estrogens [notably 2-OHE1, 2-hydroxyestradiol (2-OHE2), and 4-hydroxyestrone (4-OHE1)], which, unless methylated, can be metabolized to mutagenic catechol quinones. Several studies have in fact found decreased risks of postmenopausal breast cancer associated with elevated ratios of 2-pathway metabolites relative to parent estrogens (11, 12), and one study found increased risks for higher levels of catechols to methylated catechols (12).

For endometrial cancer, a cancer known to be influenced by epithelial cell proliferation (particularly in the absence of progesterone), metabolites that are mitogenic may be of particular interest. However, few investigations have explored the role of estrogen metabolites in endometrial carcinogenesis. One prospective study, involving 124 cases, that evaluated circulating 2-OHE1 and 16α-OHE1 levels using an enzyme immunoassay found some increases with high levels of both metabolites, but this relation did not persist after adjustment for estrone or estradiol levels (13). In another cohort study (66 cases), estradiol was significantly associated with risk, but there was no further discrimination of risk according to levels of metabolites or their ratios (14). Two endometrial cancer case–control studies have also evaluated estrogen metabolites, with suggestive relationships for certain metabolites (15, 16), although interpretation of the results was limited by small numbers and assessment of hormone levels after disease onset.

We assessed the relation of estrogen metabolites to endometrial cancer risk among participants in the Women's Health Initiative Observational Study (WHI-OS). Strengths of this study included relatively large numbers of endometrial cancers as well as availability of detailed information on risk factors, enabling a thorough assessment of confounding and interactive effects. Given recent interest in the etiologic heterogeneity of endometrial cancers, we evaluated whether the effects of estrogen metabolites differed across distinct tumor subtypes, including type I versus type II tumors, which are characterized by different hormonally related risk factor profiles (17, 18).

Study population

The WHI-OS is a prospective cohort involving 93,676 postmenopausal women, ages 50 to 79 years, enrolled at U.S. centers between 1993 and 1998 (19, 20). Excluded were 148 women who had medical conditions with a predicted survival <3 years or adherence/retention issues, or who were participating in a clinical trial. The current study, conducted as a case–control study nested in the cohort, included incident invasive endometrial cancers diagnosed between study initiation and May 2012. Study subjects were excluded if they had a history of cancer at baseline other than nonmelanoma skin cancer (n = 11,674); were current users of exogenous hormones (38,419); had a hysterectomy at baseline or during follow-up (13,862); and did not have at least 1.1 mL of available prediagnosis baseline serum (720).

Cases were identified via self-reports and medical records and centrally adjudicated. The mean time from sample collection to diagnosis was 6.9 years (SD = 3.7 years; range = 45 days–15.0 years). Controls were eligible WHI-OS cohort members selected from strata defined by age at blood draw (50–54, 55–59, 60–64, 65–69, 70–74, 75–79 years), year at blood draw (1993–1996, 1997–1998), race/ethnicity (white, black, Hispanic, other/unknown), and time since last menopausal hormone therapy (MHT) use (≤1, >1 year). Controls were alive and at risk of endometrial cancer (did not have hysterectomy) at the time of diagnosis of their matched case. Controls were shared with a nested case–control study of ovarian cancer (21) and drawn from strata containing endometrial cancer cases, with a ratio of at least 1 control per case, resulting in 313 endometrial cancer cases and 354 matched controls. Institutional review board clearance was received at the Fred Hutchinson Cancer Research Center (WHI Clinical Coordinating Center), as well as the clinical centers. All study participants provided written informed consent.

Laboratory assays

Stable isotope dilution HPLC/MS-MS was used to quantify 15 estrogens and estrogen metabolites (Fig. 1), as described previously (22). Six labeled internal standards were used: deuterated 2-hydroxyestradiol, 2-methoxyestradiol, and estriol (C/D/N Isotopes Inc); deuterated 16-epiestriol (Medical Isotopes Inc); and 13C-labeled estrone and estradiol (Cambridge Isotope Laboratories).

Figure 1.

Formation of 2-, 4-, and 16-hydroxylation pathway estrogen metabolites from parent estrogens. The current serum estrogen metabolite assay measures 15 of 17 metabolites pictured. 4-Hydroxyestradiol and 16β-hydroxyestrone (in light gray) are not measured with the current assay due to very low abundance in circulation.

Figure 1.

Formation of 2-, 4-, and 16-hydroxylation pathway estrogen metabolites from parent estrogens. The current serum estrogen metabolite assay measures 15 of 17 metabolites pictured. 4-Hydroxyestradiol and 16β-hydroxyestrone (in light gray) are not measured with the current assay due to very low abundance in circulation.

Close modal

The serum method detects 15 estrogens and estrogen metabolites which circulate primarily as sulfated and/or glucuronidated conjugates. Five estrogen metabolites (estrone, estradiol, estriol, 2-methoxyestrone, and 2-methoxyestradiol) were measured in unconjugated forms. The serum sample was split into two aliquots to measure the combined concentration of each of the 15 metabolites (sum of conjugated plus unconjugated forms) and the unconjugated forms. To measure the combined parent estrogen or estrogen metabolite level, an enzyme with sulfatase and glucuronidase activity was added to the samples to cleave any sulfate and glucoronide groups (22). To measure the unconjugated forms, the enzyme was not included in sample preparation. For metabolites with both combined and unconjugated measurements, the concentration of the conjugated form was calculated as the difference between the combined and unconjugated estrogen measurements. The limit of detection for each estrogen and estrogen metabolite measured was 10 fg on column (∼0.33–0.37 pmol/L; refs. 22, 23). No samples had undetectable hormone levels. Laboratory coefficients of variation of masked technical replicates across batches were <6.0% for all hormones measured. Intraclass correlation coefficients ranged from 0.93 to 0.996 (median value 0.98).

Statistical analysis

We included self-reported never or former MHT pill/patch users and excluded individuals with unconjugated estrone concentrations ≥184 pmol/L (∼50 pg/mL; n = 9), typically indicative of current exogenous hormone use. Individual estrogens and estrogen metabolites were categorized into quintiles based on control distributions.

Conditional logistic regression was used to estimate ORs and 95% confidence intervals (CI) of endometrial cancer risk while conditioning on matched case–control sets (determined by age and calendar year of blood draw, race/ethnicity, and time since last MHT use), and further adjusted for a priori potential confounding factors [education, body mass index (BMI), cigarette smoking status, years of oral contraception use, age at menarche, gravidity, age at menopause, never/former MHT use, and previous tubal ligation]. Additional adjustment for other variables (e.g., parity) or finer adjustment for some factors (e.g., BMI) had minimal effects on derived associations. Tests for trend were based on the Wald statistic modeling the intracategory quintile median as a continuous parameter.

For analyses stratified by clinical characteristics of the cases, we used baseline category polytomous logistic regression models, with the controls as the reference group. Analyses stratified by BMI, age at blood draw, or duration of oral contraception use were evaluated using unconditional logistic regression models. The baseline category and unconditional logistic regression models were adjusted for matching factors and a priori selected potential confounding factors (listed above), with one exception: ever and time since last MHT use were combined (never, ≤1 year, >1 year). Likelihood ratio tests for the interaction across levels of BMI, age at blood draw, or duration of oral contraception use were computed on the basis of cross-product terms with hormones categorized as the ordinal variable.

We evaluated associations stratified by histologic subtype [type I (66 adenocarcinomas, 194 endometrioid carcinomas, 11 mucinous) vs. type II (34 serous, 6 clear cell, 2 other tumors)], grade of the tumor among the endometrioid tumors and adenocarcinomas [low-grade (grades 1–2) vs. high-grade (3–4)], and time between blood collection and diagnosis (<5 year, ≥ 5 years). Differences in risk estimates across subgroups were assessed using P values (reported as Pheterogeneity or Phet) from unconditional logistic regression models that treated the largest subgroup as the reference category and excluded non-cases. We also conducted the following sensitivity analyses excluding: (i) individuals diagnosed within 2 years of blood draw (n = 27), (ii) potential outliers [greater than five SDs above the median; median excluded subjects per hormone n = 10 (min–max: 7–17)], (iii) diabetics (n = 38), and (iv) former MHT users (n = 220).

Q values which reflect FDR were calculated to account for multiple comparisons in the main analyses; all other analyses were considered exploratory and therefore not corrected for multiple comparisons. All P values were two-sided; P values <0.05 were considered statistically significant for uncorrected tests.

The endometrial cancer cases and controls were comparably aged, being 64.5 and 64.0 years, respectively (Table 1). The majority of the subjects provided blood samples during 1993–1996 and were Caucasian. Approximately 4% of the subjects reported last MHT use within the year prior to study interview.

Table 1.

Demographic and health characteristics of endometrial cancer cases and matched controls

Endometrial cancer casesControls
n = 313n = 354
Mean (SD)Mean (SD)
Age at baseline blood draw, years 64.5 (7.0) 64.0 (7.0) 
Year of blood draw n (%) n (%) 
 1993–1996 190 (60.7) 218 (61.6) 
 1997–1998 123 (39.3) 138 (39.0) 
Race/ethnicity 
 White 284 (90.7) 319 (90.1) 
 Black 15 (4.8) 17 (4.8) 
 Hispanic 2 (0.6) 3 (0.8) 
 Other 12 (3.8) 15 (4.2) 
Time since last menopausal hormone therapy use, years 
 >1 300 (95.8) 340 (96.0) 
 ≤1 13 (4.2) 14 (4.0) 
Family income 
 <$35,000 110 (35.1) 133 (37.6) 
 $35,000–$74,999 119 (38.0) 137 (38.7) 
 ≥$75,000 60 (19.2) 57 (16.1) 
Education 
 High school or less 56 (17.9) 74 (20.9) 
 Some post high school 111 (35.5) 114 (32.2) 
 College graduate 144 (46.0) 163 (46.0) 
Alcohol use, drinks/week 
 Never 33 (10.5) 32 (9.0) 
 Former 52 (16.6) 59 (16.7) 
 Current, <1 110 (35.1) 107 (30.2) 
 Current, 1–<7 68 (21.7) 94 (26.6) 
 Current, ≥7 48 (15.3) 62 (17.5) 
Smoking status 
 Never 163 (52.1) 177 (50.0) 
 Former 134 (42.8) 142 (40.1) 
 Current 13 (4.2) 32 (9.0) 
BMI, kg/m2 
 <25 74 (23.6) 161 (45.5) 
 25–29.9 90 (28.8) 104 (29.4) 
 ≥30 148 (47.3) 88 (24.9) 
Ever pregnant 
 No 43 (13.7) 55 (15.5) 
 Yes 270 (86.3) 299 (84.5) 
Duration of oral contraceptive use, years 
 Never 221 (70.6) 214 (60.5) 
 <5 50 (16.0) 72 (20.3) 
 5–<10 23 (7.3) 36 (10.2) 
 ≥10 19 (6.1) 32 (9.0) 
Age at menopause, years 
 <40 5 (1.6) 11 (3.1) 
 40–44 15 (4.8) 22 (6.2) 
 45–49 67 (21.4) 82 (23.2) 
 50–54 146 (46.6) 170 (48.0) 
 ≥55 68 (21.7) 59 (16.7) 
Menopausal hormone therapy use 
 Never 237 (75.7) 210 (59.3) 
 Former 76 (24.3) 144 (40.7) 
Tubal ligation 
 No 268 (85.6) 289 (81.6) 
 Yes 43 (13.7) 64 (18.1) 
Endometrial cancer casesControls
n = 313n = 354
Mean (SD)Mean (SD)
Age at baseline blood draw, years 64.5 (7.0) 64.0 (7.0) 
Year of blood draw n (%) n (%) 
 1993–1996 190 (60.7) 218 (61.6) 
 1997–1998 123 (39.3) 138 (39.0) 
Race/ethnicity 
 White 284 (90.7) 319 (90.1) 
 Black 15 (4.8) 17 (4.8) 
 Hispanic 2 (0.6) 3 (0.8) 
 Other 12 (3.8) 15 (4.2) 
Time since last menopausal hormone therapy use, years 
 >1 300 (95.8) 340 (96.0) 
 ≤1 13 (4.2) 14 (4.0) 
Family income 
 <$35,000 110 (35.1) 133 (37.6) 
 $35,000–$74,999 119 (38.0) 137 (38.7) 
 ≥$75,000 60 (19.2) 57 (16.1) 
Education 
 High school or less 56 (17.9) 74 (20.9) 
 Some post high school 111 (35.5) 114 (32.2) 
 College graduate 144 (46.0) 163 (46.0) 
Alcohol use, drinks/week 
 Never 33 (10.5) 32 (9.0) 
 Former 52 (16.6) 59 (16.7) 
 Current, <1 110 (35.1) 107 (30.2) 
 Current, 1–<7 68 (21.7) 94 (26.6) 
 Current, ≥7 48 (15.3) 62 (17.5) 
Smoking status 
 Never 163 (52.1) 177 (50.0) 
 Former 134 (42.8) 142 (40.1) 
 Current 13 (4.2) 32 (9.0) 
BMI, kg/m2 
 <25 74 (23.6) 161 (45.5) 
 25–29.9 90 (28.8) 104 (29.4) 
 ≥30 148 (47.3) 88 (24.9) 
Ever pregnant 
 No 43 (13.7) 55 (15.5) 
 Yes 270 (86.3) 299 (84.5) 
Duration of oral contraceptive use, years 
 Never 221 (70.6) 214 (60.5) 
 <5 50 (16.0) 72 (20.3) 
 5–<10 23 (7.3) 36 (10.2) 
 ≥10 19 (6.1) 32 (9.0) 
Age at menopause, years 
 <40 5 (1.6) 11 (3.1) 
 40–44 15 (4.8) 22 (6.2) 
 45–49 67 (21.4) 82 (23.2) 
 50–54 146 (46.6) 170 (48.0) 
 ≥55 68 (21.7) 59 (16.7) 
Menopausal hormone therapy use 
 Never 237 (75.7) 210 (59.3) 
 Former 76 (24.3) 144 (40.7) 
Tubal ligation 
 No 268 (85.6) 289 (81.6) 
 Yes 43 (13.7) 64 (18.1) 

Expected associations were seen with respect to endometrial cancer risk factors, with cases generally having higher incomes, more education, higher BMIs, earlier ages at menarche and later ages at menopause, and less often reporting current smoking, long-term oral contraceptive usage, and prior tubal ligation than controls.

Median and interdecile ranges of serum estrogen metabolites for cases versus controls are shown in Table 2. The most abundant estrogen was conjugated estrone, followed by estriol. Several metabolites were detected at quite low levels, including metabolites in the 4-hydroxylation pathway, as well as the 2-methoxy metabolites. Cases showed higher levels of all parent estrogens and individual metabolites than controls.

Table 2.

Median and interdecile range (IDR) of estrogen metabolites among endometrial cancer cases and controls

CasesControls
Estrogens and estrogen metabolites (pmol/L)Median (IDR)Median (IDR)
Parent estrogens 
 Estrone 441.4 (176.3–1239.8) 293.9 (137.5–880.9) 
  Unconjugated estrone 73.7 (37.3–155.8) 55.4 (30.1–115.9) 
  Conjugated estrone 372.2 (127.6–1096.8) 238.8 (98.1–792.1) 
 Estradiol 68.2 (29.4–172.6) 49.3 (21.9–154.7) 
  Unconjugated estradiol 20.0 (6.3–55.0) 11.6 (4–38.8) 
  Conjugated estradiol 44.2 (18.9–120) 37.1 (14.9–110.1) 
2-Hydroxylation pathway 
 2-Hydroxyestrone 80.9 (43.5–178.2) 64.9 (32.8–164) 
 2-Hydroxyestradiol 19.0 (11.0–43.0) 15.9 (8.3–40.6) 
 2-Methoxyestrone 50.8 (28.2–104.5) 41.7 (24.8–89.5) 
  Unconjugated 2-methoxyestrone 12.8 (6.3–26.4) 10.4 (4.4–23.3) 
  Conjugated 2-methoxyestrone 36.2 (18.4–85.8) 31.8 (16.9–73.5) 
 2-Methoxyestradiol 15.9 (8.0–36.8) 12.4 (6.6–32.9) 
  Unconjugated 2-methoxyestradiol 2.7 (1.4–6.5) 2.0 (1.1–4.8) 
  Conjugated 2-methoxyestradiol 12.8 (6.3–34.4) 10.5 (5.1–28.1) 
 2-Hydroxyestrone-3-methyl ether 9.1 (5.1–19.0) 7.6 (4.2–17.1) 
4-Hydroxylation pathway 
 4-Hydroxyestrone 9.5 (5.1–24.0) 7.6 (4.1–21.1) 
 4-Methoxyestrone 4.6 (3.2–14.1) 3.9 (2.8–10.5) 
 4-Methoxyestradiol 2.1 (1.2–5.6) 1.7 (0.9–4.1) 
16α-Hydroxylation pathway 
 16α-Hydroxyestrone 40.9 (21.3–90.9) 32.3 (15.8–86.8) 
 Estriol 181.3 (87.8–421.9) 140.4 (63.5–391.5) 
  Unconjugated estriol 34.1 (15.4–74.4) 25.7 (12.2–63.7) 
  Conjugated estriol 146.9 (66.1–352.6) 109.7 (49.3–332) 
 16-Ketoestradiol 45.1 (22.3–109.5) 34.2 (16.6–101.3) 
 16-Epiestriol 18.5 (9.6–40.9) 15.0 (7.5–38.3) 
 17-Epiestriol 15.6 (7.9–37.3) 12.8 (6.2–31.7) 
CasesControls
Estrogens and estrogen metabolites (pmol/L)Median (IDR)Median (IDR)
Parent estrogens 
 Estrone 441.4 (176.3–1239.8) 293.9 (137.5–880.9) 
  Unconjugated estrone 73.7 (37.3–155.8) 55.4 (30.1–115.9) 
  Conjugated estrone 372.2 (127.6–1096.8) 238.8 (98.1–792.1) 
 Estradiol 68.2 (29.4–172.6) 49.3 (21.9–154.7) 
  Unconjugated estradiol 20.0 (6.3–55.0) 11.6 (4–38.8) 
  Conjugated estradiol 44.2 (18.9–120) 37.1 (14.9–110.1) 
2-Hydroxylation pathway 
 2-Hydroxyestrone 80.9 (43.5–178.2) 64.9 (32.8–164) 
 2-Hydroxyestradiol 19.0 (11.0–43.0) 15.9 (8.3–40.6) 
 2-Methoxyestrone 50.8 (28.2–104.5) 41.7 (24.8–89.5) 
  Unconjugated 2-methoxyestrone 12.8 (6.3–26.4) 10.4 (4.4–23.3) 
  Conjugated 2-methoxyestrone 36.2 (18.4–85.8) 31.8 (16.9–73.5) 
 2-Methoxyestradiol 15.9 (8.0–36.8) 12.4 (6.6–32.9) 
  Unconjugated 2-methoxyestradiol 2.7 (1.4–6.5) 2.0 (1.1–4.8) 
  Conjugated 2-methoxyestradiol 12.8 (6.3–34.4) 10.5 (5.1–28.1) 
 2-Hydroxyestrone-3-methyl ether 9.1 (5.1–19.0) 7.6 (4.2–17.1) 
4-Hydroxylation pathway 
 4-Hydroxyestrone 9.5 (5.1–24.0) 7.6 (4.1–21.1) 
 4-Methoxyestrone 4.6 (3.2–14.1) 3.9 (2.8–10.5) 
 4-Methoxyestradiol 2.1 (1.2–5.6) 1.7 (0.9–4.1) 
16α-Hydroxylation pathway 
 16α-Hydroxyestrone 40.9 (21.3–90.9) 32.3 (15.8–86.8) 
 Estriol 181.3 (87.8–421.9) 140.4 (63.5–391.5) 
  Unconjugated estriol 34.1 (15.4–74.4) 25.7 (12.2–63.7) 
  Conjugated estriol 146.9 (66.1–352.6) 109.7 (49.3–332) 
 16-Ketoestradiol 45.1 (22.3–109.5) 34.2 (16.6–101.3) 
 16-Epiestriol 18.5 (9.6–40.9) 15.0 (7.5–38.3) 
 17-Epiestriol 15.6 (7.9–37.3) 12.8 (6.2–31.7) 

Adjusted ORs associated with the 5th versus 1st quintile of the parent estrogens were 3.19 (95% CI, 1.69–6.04) for estrone and 1.41 (0.75–2.67) for estradiol (Table 3). There was little difference in the association between unconjugated and conjugated estrone, but for estradiol the difference in risk was striking, being 6.19 (2.95–13.03) for unconjugated estradiol and 0.95 (0.51–1.77) for conjugated estradiol. There were significant trends across quintiles of estrone, regardless of conjugation, and for unconjugated estradiol (individual quintile ORs are shown in Supplementary Table S1).

Table 3.

Risk of endometrial cancer comparing the 5th to the 1st quintile for each estrogen metabolite, before and after adjustment for unconjugated estradiol

ORa (95% CI)PtrendbFDRORc (95% CI)Ptrendb
Parent estrogens 
 Estrone 3.19 (1.69–6.04) 0.0001 0.0004 2.70 (1.34–5.45) 0.003 
  Unconjugated estrone 2.70 (1.48–4.92) 0.0002 0.0005 2.23 (1.10–4.51) 0.017 
  Conjugated estrone 2.98 (1.59–5.58) 0.0002 0.0005 2.46 (1.25–4.85) 0.010 
 Estradiol 1.41 (0.75–2.67) 0.4531 0.4720   
  Unconjugated estradiol 6.19 (2.95–13.03) 0.0001 0.0004   
  Conjugated estradiol 0.95 (0.51–1.77) 0.6747 0.6747   
2-Hydroxylation pathway 
 2-Hydroxyestrone 3.00 (1.56–5.78) 0.0033 0.0055 2.41 (1.21–4.82) 0.048 
 2-Hydroxyestradiol 2.31 (1.22–4.37) 0.0328 0.0373 1.82 (0.93–3.55) 0.237 
 2-Methoxyestrone 2.12 (1.16–3.88) 0.0022 0.0042 1.77 (0.94–3.33) 0.025 
  Unconjugated 2-methoxyestrone 2.69 (1.46–4.96) 0.0049 0.0074 2.00 (1.03–3.89) 0.099 
  Conjugated 2-methoxyestrone 1.60 (0.90–2.86) 0.0246 0.0293 2.86 (1.45–5.64) 0.001 
 2-Methoxyestradiol 3.35 (1.76–6.37) 0.0001 0.0004 2.45 (1.23–4.85) 0.018 
  Unconjugated 2-methoxyestradiol 3.06 (1.63–5.73) 0.0006 0.0014 2.73 (1.39–5.37) 0.003 
  Conjugated 2-methoxyestradiol 3.26 (1.70–6.25) 0.0002 0.0005 2.25 (1.13–4.48) 0.233 
 2-Hydroxyestrone-3-methyl ether 2.83 (1.45–5.51) 0.0361 0.0392 2.45 (1.24–4.84) 0.025 
4-Hydroxylation pathway 
 4-Hydroxyestrone 3.04 (1.59–5.80) 0.0019 0.0040 2.46 (1.31–4.60) 0.001 
 4-Methoxyestrone 2.89 (1.57–5.31) 0.0001 0.0004 3.01 (1.51–6.03) 0.001 
 4-Methoxyestradiol 3.52 (1.82–6.80) 0.0001 0.0004 2.19 (1.12–4.29) 0.063 
16α-Hydroxylation pathway 
 16α-Hydroxyestrone 2.73 (1.44–5.16) 0.0050 0.0074 3.29 (1.66–6.51) 0.004 
 Estriol 4.00 (2.09–7.67) 0.0001 0.0004 1.37 (0.76–2.48) 0.101 
  Unconjugated estriol 3.25 (1.71–6.19) 0.0002 0.0005 2.69 (1.36–5.33) 0.005 
  Conjugated estriol 3.37 (1.75–6.49) 0.0032 0.0055 2.54 (1.28–5.04) 0.058 
 16-Ketoestradiol 3.13 (1.63–6.03) 0.0053 0.0074 2.77 (1.40–5.46) 0.034 
 16-Epiestriol 2.88 (1.49–5.54) 0.0060 0.0079 2.30 (1.17–4.56) 0.086 
 17-Epiestriol 2.30 (1.23–4.31) 0.0146 0.0183 1.78 (0.92–3.44) 0.181 
ORa (95% CI)PtrendbFDRORc (95% CI)Ptrendb
Parent estrogens 
 Estrone 3.19 (1.69–6.04) 0.0001 0.0004 2.70 (1.34–5.45) 0.003 
  Unconjugated estrone 2.70 (1.48–4.92) 0.0002 0.0005 2.23 (1.10–4.51) 0.017 
  Conjugated estrone 2.98 (1.59–5.58) 0.0002 0.0005 2.46 (1.25–4.85) 0.010 
 Estradiol 1.41 (0.75–2.67) 0.4531 0.4720   
  Unconjugated estradiol 6.19 (2.95–13.03) 0.0001 0.0004   
  Conjugated estradiol 0.95 (0.51–1.77) 0.6747 0.6747   
2-Hydroxylation pathway 
 2-Hydroxyestrone 3.00 (1.56–5.78) 0.0033 0.0055 2.41 (1.21–4.82) 0.048 
 2-Hydroxyestradiol 2.31 (1.22–4.37) 0.0328 0.0373 1.82 (0.93–3.55) 0.237 
 2-Methoxyestrone 2.12 (1.16–3.88) 0.0022 0.0042 1.77 (0.94–3.33) 0.025 
  Unconjugated 2-methoxyestrone 2.69 (1.46–4.96) 0.0049 0.0074 2.00 (1.03–3.89) 0.099 
  Conjugated 2-methoxyestrone 1.60 (0.90–2.86) 0.0246 0.0293 2.86 (1.45–5.64) 0.001 
 2-Methoxyestradiol 3.35 (1.76–6.37) 0.0001 0.0004 2.45 (1.23–4.85) 0.018 
  Unconjugated 2-methoxyestradiol 3.06 (1.63–5.73) 0.0006 0.0014 2.73 (1.39–5.37) 0.003 
  Conjugated 2-methoxyestradiol 3.26 (1.70–6.25) 0.0002 0.0005 2.25 (1.13–4.48) 0.233 
 2-Hydroxyestrone-3-methyl ether 2.83 (1.45–5.51) 0.0361 0.0392 2.45 (1.24–4.84) 0.025 
4-Hydroxylation pathway 
 4-Hydroxyestrone 3.04 (1.59–5.80) 0.0019 0.0040 2.46 (1.31–4.60) 0.001 
 4-Methoxyestrone 2.89 (1.57–5.31) 0.0001 0.0004 3.01 (1.51–6.03) 0.001 
 4-Methoxyestradiol 3.52 (1.82–6.80) 0.0001 0.0004 2.19 (1.12–4.29) 0.063 
16α-Hydroxylation pathway 
 16α-Hydroxyestrone 2.73 (1.44–5.16) 0.0050 0.0074 3.29 (1.66–6.51) 0.004 
 Estriol 4.00 (2.09–7.67) 0.0001 0.0004 1.37 (0.76–2.48) 0.101 
  Unconjugated estriol 3.25 (1.71–6.19) 0.0002 0.0005 2.69 (1.36–5.33) 0.005 
  Conjugated estriol 3.37 (1.75–6.49) 0.0032 0.0055 2.54 (1.28–5.04) 0.058 
 16-Ketoestradiol 3.13 (1.63–6.03) 0.0053 0.0074 2.77 (1.40–5.46) 0.034 
 16-Epiestriol 2.88 (1.49–5.54) 0.0060 0.0079 2.30 (1.17–4.56) 0.086 
 17-Epiestriol 2.30 (1.23–4.31) 0.0146 0.0183 1.78 (0.92–3.44) 0.181 

aOR (quintile 5 vs. quintile 1) from model conditioned on matching factors [age at baseline, calendar year of blood draw, race/ethnicity, and recency of MHT use (≤1/>1 year)] and adjusted for education, BMI, cigarette smoking status, years of oral contraceptive use, age at menarche, gravidity, age at menopause, never/former MHT use, and previous tubal ligation.

bP values for trend across quintile (median value of category).

cSame model as 1, also adjusted for unconjugated estradiol.

Nearly all of the individual metabolites also showed significant linear trends and associations with risk (the one exception being conjugated 2-methoxyestrone), with the magnitude of the risks ranging from 2.1 to 4.0. We cautiously (given high correlations of estrogens and metabolites, see Supplementary Table S2) also examined ratios of different estrogens and metabolites; however, we observed no convincing or statistically significant patterns of risk associated with these quantities (results not shown).

When we adjusted all other estrogens and metabolites for the strongest predictor of risk, namely, unconjugated estradiol (as a continuous variable; Table 3), we generally saw some attenuation in the observed risks, and several metabolite associations became nonsignificant (2-hydroxyestradiol, 2-methoxyestrone, estriol, 17-epiestriol). However, a number of the metabolites remained associated with risk, showing significant associations for the highest quintiles (magnitude of association 2.0–3.0) and significant linear trends.

As endogenous estrogens are known to be correlated with BMI, we assessed relations of the various estrogens and metabolites across different BMI categories. This demonstrated that estrogens were generally associated with increased risks across all BMI categories (parent estrogens shown in Table 4 and estrogen metabolites in Supplementary Table S3). Similar analyses were pursued according to different categories of age at diagnosis and years of use of oral contraceptives. While there was no evidence of interactive effects of estrogens with oral contraceptive usage, some of the estrogens showed stronger relations for older subjects, with interactions being statistically significant at P < 0.05 for conjugated 2-methoxyestradiol, 4-methoxyestrone, and 17-epiestriol.

Table 4.

Risk of endometrial cancer comparing the 5th to the 1st quintile for parent estrogens across categories of BMI, age, and years of oral contraceptive use

BMIORa (95% CI)PtrendPinteractionAgeORa (95% CI)PtrendPinteractionYears of OC useORa (95% CI)PtrendPinteraction
Parent estrogens 
Estrone 
  <25 3.62 (1.00–13.11) 0.02 0.41 <60 2.44 (0.63–9.44) 0.25 0.36 Never 2.12 (1.00–4.49) 0.01 0.10 
  25–29.9 1.08 (0.33–3.54) 0.29  60–69 2.60 (1.03–6.54) 0.003  <5 years 14.52 (2.25–93.77) 0.01  
  ≥30 8.06 (1.82–35.77) 0.004  ≥70 10.60 (2.80–40.10) 0.001  ≥5 years 15.15 (0.79–292.14) 0.02  
 Unconjugated estrone 
  <25 3.35 (1.16–9.69) 0.01 0.50 <60 2.90 (0.81–10.42) 0.17 0.23 Never 1.71 (0.85–3.44) 0.04 0.12 
  25–29.9 1.16 (0.39–3.43) 0.48  60–69 2.46 (1.02–5.92) 0.05  <5 years 29.90 (4.08–219.16) 0.003  
  ≥30 6.00 (1.51–23.94) 0.02  ≥70 4.45 (1.29–15.29) 0.001  ≥5 years 7.12 (0.50–100.97) 0.008  
 Conjugated estrone 
  <25 3.43 (1.05–11.26) 0.03 0.53 <60 2.53 (0.67–9.56) 0.22 0.10 Never 2.01 (0.95–4.26) 0.04 0.15 
  25–29.9 1.19 (0.35–4.02) 0.32  60–69 2.45 (0.99–6.09) 0.009  <5 years 10.60 (2.12–53.14) 0.005  
  ≥30 7.89 (2.02–30.77) 0.01  ≥70 8.10 (2.23–29.46) 0.003  ≥5 years 7.43 (0.39–142.68) 0.06  
Estradiol 
  <25 0.88 (0.25–3.03) 0.86 0.30 <60 2.76 (0.70–10.94) 0.59 0.08 Never 1.22 (0.57–2.60) 0.33 0.36 
  25–29.9 0.52 (0.16–1.67) 0.37  60–69 0.92 (0.33–2.52) 0.76  <5 years 3.75 (0.54–26.15) 0.69  
  ≥30 6.56 (1.06–40.51) 0.05  ≥70 1.53 (0.48–4.87) 0.51  ≥5 years 6.23 (0.45–85.47) 0.52  
 Unconjugated estradiol 
  <25 7.84 (2.1–29.22) 0.01 0.48 <60 8.74 (1.47–51.92) 0.17 0.50 Never 4.19 (1.84–9.56) 0.01 0.25 
  25–29.9 2.39 (0.64–8.99) 0.06  60–69 4.82 (1.60–14.52) 0.04  <5 years b 0.002  
  ≥30 6.60 (1.02–42.75) 0.05  ≥70 12.61 (3.17–50.13) 0.001  ≥5 years 4.62 (0.29–74.7) 0.05  
 Conjugated estradiol 
  <25 0.79 (0.23–2.74) 0.79 0.16 <60 1.85 (0.55–6.25) 0.64 0.24 Never 0.78 (0.37–1.66) 0.66 0.10 
  25–29.9 0.29 (0.09–0.94) 0.08  60–69 0.68 (0.25–1.83) 0.41  <5 years 1.26 (0.22–7.16) 0.99  
  ≥30 5.31 (0.87–32.4) 0.21  ≥70 0.68 (0.20–2.29) 0.86  ≥5 years 7.41 (0.54–100.96) 0.19  
BMIORa (95% CI)PtrendPinteractionAgeORa (95% CI)PtrendPinteractionYears of OC useORa (95% CI)PtrendPinteraction
Parent estrogens 
Estrone 
  <25 3.62 (1.00–13.11) 0.02 0.41 <60 2.44 (0.63–9.44) 0.25 0.36 Never 2.12 (1.00–4.49) 0.01 0.10 
  25–29.9 1.08 (0.33–3.54) 0.29  60–69 2.60 (1.03–6.54) 0.003  <5 years 14.52 (2.25–93.77) 0.01  
  ≥30 8.06 (1.82–35.77) 0.004  ≥70 10.60 (2.80–40.10) 0.001  ≥5 years 15.15 (0.79–292.14) 0.02  
 Unconjugated estrone 
  <25 3.35 (1.16–9.69) 0.01 0.50 <60 2.90 (0.81–10.42) 0.17 0.23 Never 1.71 (0.85–3.44) 0.04 0.12 
  25–29.9 1.16 (0.39–3.43) 0.48  60–69 2.46 (1.02–5.92) 0.05  <5 years 29.90 (4.08–219.16) 0.003  
  ≥30 6.00 (1.51–23.94) 0.02  ≥70 4.45 (1.29–15.29) 0.001  ≥5 years 7.12 (0.50–100.97) 0.008  
 Conjugated estrone 
  <25 3.43 (1.05–11.26) 0.03 0.53 <60 2.53 (0.67–9.56) 0.22 0.10 Never 2.01 (0.95–4.26) 0.04 0.15 
  25–29.9 1.19 (0.35–4.02) 0.32  60–69 2.45 (0.99–6.09) 0.009  <5 years 10.60 (2.12–53.14) 0.005  
  ≥30 7.89 (2.02–30.77) 0.01  ≥70 8.10 (2.23–29.46) 0.003  ≥5 years 7.43 (0.39–142.68) 0.06  
Estradiol 
  <25 0.88 (0.25–3.03) 0.86 0.30 <60 2.76 (0.70–10.94) 0.59 0.08 Never 1.22 (0.57–2.60) 0.33 0.36 
  25–29.9 0.52 (0.16–1.67) 0.37  60–69 0.92 (0.33–2.52) 0.76  <5 years 3.75 (0.54–26.15) 0.69  
  ≥30 6.56 (1.06–40.51) 0.05  ≥70 1.53 (0.48–4.87) 0.51  ≥5 years 6.23 (0.45–85.47) 0.52  
 Unconjugated estradiol 
  <25 7.84 (2.1–29.22) 0.01 0.48 <60 8.74 (1.47–51.92) 0.17 0.50 Never 4.19 (1.84–9.56) 0.01 0.25 
  25–29.9 2.39 (0.64–8.99) 0.06  60–69 4.82 (1.60–14.52) 0.04  <5 years b 0.002  
  ≥30 6.60 (1.02–42.75) 0.05  ≥70 12.61 (3.17–50.13) 0.001  ≥5 years 4.62 (0.29–74.7) 0.05  
 Conjugated estradiol 
  <25 0.79 (0.23–2.74) 0.79 0.16 <60 1.85 (0.55–6.25) 0.64 0.24 Never 0.78 (0.37–1.66) 0.66 0.10 
  25–29.9 0.29 (0.09–0.94) 0.08  60–69 0.68 (0.25–1.83) 0.41  <5 years 1.26 (0.22–7.16) 0.99  
  ≥30 5.31 (0.87–32.4) 0.21  ≥70 0.68 (0.20–2.29) 0.86  ≥5 years 7.41 (0.54–100.96) 0.19  

aOR (quintile 5 vs. quintile 1) from model adjusted for matching factors [age at baseline, calendar year of blood draw, race/ethnicity, and recency of MHT use (never, ≤1/>1 year)] and education, cigarette smoking status, age at menarche, gravidity, age at menopause, and previous tubal ligation. Additional adjustment was made for BMI and years of oral contraceptive use, if relevant.

bCould not be estimated; too few cases in reference category.

We also assessed the extent to which estrogens might explain the effects of obesity on endometrial cancer risk, comparing BMI estimates in models unadjusted for estrogens with estrogen-adjusted estimates. Without adjustment for estrogens and compared with a referent group of BMI < 25, the ORs were 2.17 (95% CI, 1.40–3.34) for BMI 25–29.9 and 3.97 (2.54–6.21) for BMI ≥ 30. Additional adjustment for unconjugated estradiol resulted in an attenuation of these risks to 1.55 (0.97–2.48) and 2.25 (1.33–3.81), respectively.

Given interest in the etiologic heterogeneity of endometrial cancer, we also examined relations of the estrogens and metabolites according to several clinical characteristics (Table 5). A total of 271 (86.6%) cases were classified as type I and 42 (13.4%) as type II tumors. Significant heterogeneity in the associations of several estrogens were seen between the two tumor types, including unconjugated estradiol [OR for highest vs. lowest quintile for type I tumors was 6.97 (95% CI, 3.20–15.20) vs. 1.80 (0.43–7.49) for type II tumors, Phet = 0.01]. Other significant differences were seen for unconjugated 2-methoxyestrone (3.47 vs. 0.95), 4-methoxyestrone (3.54 vs. 0.84), and unconjugated estriol (3.34 vs. 1.83). When we further limited the analyses to endometrioid tumors and adenocarcinomas and assessed whether there were differences in estrogen associations according to grade of the tumors, we observed stronger associations of unconjugated estradiol with risks of low-grade versus high-grade tumors (OR 8.92 vs. 3.27), but the difference was not statistically significant (Phet = 0.14).

Table 5.

Risk of endometrial cancer comparing the 5th to the 1st quintile for each estrogen metabolite: subtype analyses according to tumor type (I vs. II) and grade (low- vs. high-grade)

Type IType IILow gradeHigh grade
(n = 271)(n = 42)(n = 189)(n = 65)
Parent estrogensORa (95% CI)PtrendbORa (95% CI)PtrendbPhetORa (95% CI)PtrendbORa (95% CI)PtrendbPhet
 Estrone 3.41 (1.79–6.50) <0.001 3.39 (0.90–12.73) 0.14 0.48 3.38 (1.65–6.96) <0.001 3.16 (1.09–9.13) 0.01 0.63 
  Unconjugated estrone 2.91 (1.58–5.37) <0.001 1.50 (0.46–4.87) 0.69 0.07 2.65 (1.34–5.21) <0.001 2.51 (0.89–7.08) 0.11 0.27 
  Conjugated estrone 3.04 (1.62–5.70) <0.001 4.22 (1.02–17.54) 0.15 0.60 3.00 (1.49–6.06) <0.001 2.67 (0.98–7.29) 0.03 0.68 
 Estradiol 1.70 (0.89–3.25) 0.13 0.76 (0.22–2.62) 0.67 0.29 1.48 (0.72–3.04) 0.16 1.89 (0.54–6.62) 0.98 0.35 
  Unconjugated estradiol 6.97 (3.20–15.20) <0.001 1.80 (0.43–7.49) 0.83 0.01 8.92 (3.38–23.54) <0.001 3.27 (1.03–10.36) 0.09 0.14 
  Conjugated estradiol 1.16 (0.62–2.19) 0.64 0.48 (0.13–1.77) 0.28 0.26 1.05 (0.52–2.13) 0.50 1.26 (0.39–4.08) 0.57 0.45 
2-Hydroxylation pathway 
 2-Hydroxyestrone 2.99 (1.55–5.78) <0.001 3.38 (0.58–19.67) 0.78 0.16 3.56 (1.65–7.69) 0.001 2.30 (0.81–6.48) 0.06 0.62 
 2-Hydroxyestradiol 2.43 (1.28–4.63) 0.008 2.56 (0.56–11.72) 0.71 0.40 3.16 (1.47–6.82) 0.006 1.63 (0.62–4.29) 0.16 0.62 
 2-Methoxyestrone 2.51 (1.36–4.65) <0.001 0.90 (0.28–2.90) 0.81 0.16 2.27 (1.16–4.45) 0.001 3.94 (1.30–11.92) 0.01 0.93 
  Unconjugated 2-methoxyestrone 3.47 (1.82–6.62) <0.001 0.95 (0.30–3.05) 0.74 0.02 3.40 (1.63–7.11) 0.003 3.45 (1.16–10.23) 0.03 0.72 
  Conjugated 2-methoxyestrone 1.71 (0.95–3.08) 0.007 1.19 (0.37–3.84) 0.53 0.67 1.62 (0.85–3.09) 0.01 1.99 (0.77–5.13) 0.07 0.97 
 2-Methoxyestradiol 4.19 (2.18–8.07) <0.001 1.48 (0.43–5.08) 0.66 0.08 3.50 (1.68–7.28) <0.001 5.14 (1.76–14.99) 0.00 0.42 
  Unconjugated 2-methoxyestradiol 3.85 (1.99–7.45) <0.001 1.68 (0.52–5.43) 0.55 0.20 3.43 (1.63–7.25) <0.001 4.07 (1.33–12.45) 0.01 0.76 
  Conjugated 2-methoxyestradiol 3.79 (1.97–7.29) <0.001 1.97 (0.52–7.41) 0.51 0.15 3.35 (1.61–6.94) <0.001 4.03 (1.38–11.78) 0.01 0.87 
 2-Hydroxyestrone-3-methyl ether 3.58 (1.80–7.11) 0.004 1.08 (0.25–4.60) 0.81 0.17 3.93 (1.80–8.58) 0.003 2.33 (0.73–7.43) 0.43 0.18 
4-Hydroxylation pathway 
 4-Hydroxyestrone 3.19 (1.67–6.11) <0.001 2.73 (0.59–12.63) 0.82 0.12 4.17 (1.93–9.03) <0.001 1.91 (0.72–5.08) 0.07 0.55 
 4-Methoxyestrone 3.54 (1.91–6.59) <0.001 0.84 (0.23–3.06) 0.96 0.03 3.20 (1.61–6.37) <0.001 4.13 (1.6–10.66) 0.00 0.30 
 4-Methoxyestradiol 4.00 (2.06–7.79) <0.001 2.23 (0.59–8.45) 0.44 0.12 3.70 (1.75–7.83) <0.001 3.60 (1.31–9.90) 0.00 0.80 
16α-Hydroxylation pathway 
 16α-Hydroxyestrone 2.84 (1.49–5.41) 0.001 2.23 (0.47–10.61) 0.91 0.14 3.10 (1.48–6.50) 0.002 2.50 (0.90–6.96) 0.05 0.83 
 Estriol 4.14 (2.14–8.00) <0.001 3.38 (0.75–15.20) 0.34 0.21 4.85 (2.20–10.66) <0.001 3.53 (1.32–9.46) 0.00 0.40 
  Unconjugated estriol 3.34 (1.75–6.35) <0.001 1.83 (0.43–7.84) 0.88 0.03 3.02 (1.47–6.19) <0.001 4.05 (1.39–11.77) 0.01 0.84 
  Conjugated estriol 3.35 (1.73–6.45) <0.001 4.60 (0.85–25.08) 0.40 0.38 3.69 (1.71–7.96) 0.003 3.23 (1.17–8.93) 0.01 0.54 
 16-Ketoestradiol 3.23 (1.67–6.27) 0.002 3.27 (0.74–14.51) 0.52 0.32 3.59 (1.65–7.79) 0.004 2.65 (0.95–7.40) 0.03 0.90 
 16-Epiestriol 3.33 (1.70–6.54) 0.001 1.35 (0.32–5.66) 0.99 0.11 4.43 (1.96–9.98) <0.001 2.21 (0.76–6.46) 0.19 0.29 
 17-Epiestriol 2.57 (1.36–4.85) 0.005 1.60 (0.40–6.39) 0.60 0.40 3.62 (1.66–7.92) 0.006 1.33 (0.53–3.35) 0.17 0.53 
Type IType IILow gradeHigh grade
(n = 271)(n = 42)(n = 189)(n = 65)
Parent estrogensORa (95% CI)PtrendbORa (95% CI)PtrendbPhetORa (95% CI)PtrendbORa (95% CI)PtrendbPhet
 Estrone 3.41 (1.79–6.50) <0.001 3.39 (0.90–12.73) 0.14 0.48 3.38 (1.65–6.96) <0.001 3.16 (1.09–9.13) 0.01 0.63 
  Unconjugated estrone 2.91 (1.58–5.37) <0.001 1.50 (0.46–4.87) 0.69 0.07 2.65 (1.34–5.21) <0.001 2.51 (0.89–7.08) 0.11 0.27 
  Conjugated estrone 3.04 (1.62–5.70) <0.001 4.22 (1.02–17.54) 0.15 0.60 3.00 (1.49–6.06) <0.001 2.67 (0.98–7.29) 0.03 0.68 
 Estradiol 1.70 (0.89–3.25) 0.13 0.76 (0.22–2.62) 0.67 0.29 1.48 (0.72–3.04) 0.16 1.89 (0.54–6.62) 0.98 0.35 
  Unconjugated estradiol 6.97 (3.20–15.20) <0.001 1.80 (0.43–7.49) 0.83 0.01 8.92 (3.38–23.54) <0.001 3.27 (1.03–10.36) 0.09 0.14 
  Conjugated estradiol 1.16 (0.62–2.19) 0.64 0.48 (0.13–1.77) 0.28 0.26 1.05 (0.52–2.13) 0.50 1.26 (0.39–4.08) 0.57 0.45 
2-Hydroxylation pathway 
 2-Hydroxyestrone 2.99 (1.55–5.78) <0.001 3.38 (0.58–19.67) 0.78 0.16 3.56 (1.65–7.69) 0.001 2.30 (0.81–6.48) 0.06 0.62 
 2-Hydroxyestradiol 2.43 (1.28–4.63) 0.008 2.56 (0.56–11.72) 0.71 0.40 3.16 (1.47–6.82) 0.006 1.63 (0.62–4.29) 0.16 0.62 
 2-Methoxyestrone 2.51 (1.36–4.65) <0.001 0.90 (0.28–2.90) 0.81 0.16 2.27 (1.16–4.45) 0.001 3.94 (1.30–11.92) 0.01 0.93 
  Unconjugated 2-methoxyestrone 3.47 (1.82–6.62) <0.001 0.95 (0.30–3.05) 0.74 0.02 3.40 (1.63–7.11) 0.003 3.45 (1.16–10.23) 0.03 0.72 
  Conjugated 2-methoxyestrone 1.71 (0.95–3.08) 0.007 1.19 (0.37–3.84) 0.53 0.67 1.62 (0.85–3.09) 0.01 1.99 (0.77–5.13) 0.07 0.97 
 2-Methoxyestradiol 4.19 (2.18–8.07) <0.001 1.48 (0.43–5.08) 0.66 0.08 3.50 (1.68–7.28) <0.001 5.14 (1.76–14.99) 0.00 0.42 
  Unconjugated 2-methoxyestradiol 3.85 (1.99–7.45) <0.001 1.68 (0.52–5.43) 0.55 0.20 3.43 (1.63–7.25) <0.001 4.07 (1.33–12.45) 0.01 0.76 
  Conjugated 2-methoxyestradiol 3.79 (1.97–7.29) <0.001 1.97 (0.52–7.41) 0.51 0.15 3.35 (1.61–6.94) <0.001 4.03 (1.38–11.78) 0.01 0.87 
 2-Hydroxyestrone-3-methyl ether 3.58 (1.80–7.11) 0.004 1.08 (0.25–4.60) 0.81 0.17 3.93 (1.80–8.58) 0.003 2.33 (0.73–7.43) 0.43 0.18 
4-Hydroxylation pathway 
 4-Hydroxyestrone 3.19 (1.67–6.11) <0.001 2.73 (0.59–12.63) 0.82 0.12 4.17 (1.93–9.03) <0.001 1.91 (0.72–5.08) 0.07 0.55 
 4-Methoxyestrone 3.54 (1.91–6.59) <0.001 0.84 (0.23–3.06) 0.96 0.03 3.20 (1.61–6.37) <0.001 4.13 (1.6–10.66) 0.00 0.30 
 4-Methoxyestradiol 4.00 (2.06–7.79) <0.001 2.23 (0.59–8.45) 0.44 0.12 3.70 (1.75–7.83) <0.001 3.60 (1.31–9.90) 0.00 0.80 
16α-Hydroxylation pathway 
 16α-Hydroxyestrone 2.84 (1.49–5.41) 0.001 2.23 (0.47–10.61) 0.91 0.14 3.10 (1.48–6.50) 0.002 2.50 (0.90–6.96) 0.05 0.83 
 Estriol 4.14 (2.14–8.00) <0.001 3.38 (0.75–15.20) 0.34 0.21 4.85 (2.20–10.66) <0.001 3.53 (1.32–9.46) 0.00 0.40 
  Unconjugated estriol 3.34 (1.75–6.35) <0.001 1.83 (0.43–7.84) 0.88 0.03 3.02 (1.47–6.19) <0.001 4.05 (1.39–11.77) 0.01 0.84 
  Conjugated estriol 3.35 (1.73–6.45) <0.001 4.60 (0.85–25.08) 0.40 0.38 3.69 (1.71–7.96) 0.003 3.23 (1.17–8.93) 0.01 0.54 
 16-Ketoestradiol 3.23 (1.67–6.27) 0.002 3.27 (0.74–14.51) 0.52 0.32 3.59 (1.65–7.79) 0.004 2.65 (0.95–7.40) 0.03 0.90 
 16-Epiestriol 3.33 (1.70–6.54) 0.001 1.35 (0.32–5.66) 0.99 0.11 4.43 (1.96–9.98) <0.001 2.21 (0.76–6.46) 0.19 0.29 
 17-Epiestriol 2.57 (1.36–4.85) 0.005 1.60 (0.40–6.39) 0.60 0.40 3.62 (1.66–7.92) 0.006 1.33 (0.53–3.35) 0.17 0.53 

NOTE: Type I (66 adenocarcinomas, 194 endometrioid carcinomas, 11 mucinous) vs. type II (34 serous, 6 clear cell, 2 other); grade of tumor (low = grade 1, 2, high = grade 3, 4) evaluated among endometrioid carcinomas and adenocarcinomas only.

aOR (quintile 5 vs. quintile 1) from model adjusted for matching factors [age at baseline, calendar year of blood draw, race/ethnicity, and recency of MHT use (never, ≤1/>1 year)] and education, BMI, cigarette smoking status, years of oral contracteptive use, age at menarche, gravidity, age at menopause, and previous tubal ligation.

bP values for trend across quintile (median value of category).

Associations were not significantly different by time since blood draw (<5/≥5 years). In sensitivity analyses, ORs excluding cases diagnosed within 2 years of blood draw or diabetics remained unchanged. We also excluded individuals with outlier estrogen measurements, but given the small numbers involved this had minimal effects on derived associations. Finally, we restricted analyses to never users of MHT (excluding former users) and did not observe large alterations from previously derived risks.

In this largest study to date addressing the relation of endogenous estrogens and estrogen metabolites to endometrial cancer risk, we found that endometrial cancer risk was directly associated with serum levels of endogenous estrogens, with the highest risks associated with levels of unconjugated estradiol. Using a highly sensitive, accurate, and reproducible assay, we found that the association with unconjugated estradiol was stronger than generally has been seen with less robust assays, with subjects in the highest quintile showing a 6-fold increased risk compared with those in the lowest quintile. After adjustment for unconjugated estradiol, the associations with the other estrogens and metabolites were attenuated, but most continued to show risk elevations on the order to 2- to 3-fold for women in the highest versus lowest quintiles.

Our findings provided little support for varying effects of different estrogen metabolites on endometrial cancer risk, in line with two prior smaller prospective studies (13, 14). Dissimilar to our hypothesis that endometrial cancer might be affected by metabolites that have unique mitogenic properties, and in contrast to finding from several breast cancer studies (9, 11), we did not observe distinctive associations with high ratios of the 2- to 16-pathway estrogens. We also found no support for mutagenicity given that endometrial cancer risk was not related to increased levels of catechols to methylated catechols. Divergent findings for breast and endometrial cancer are further supported by experimental data, which fail to support unique antineoplastic activity of 2-hydroxy metabolites in endometrial tissue (24, 25) and instead are consistent with all three pathways (2, 4, and 16) having uterotropic activity that can result in endometrial proliferation (26) and endometrial tumor progression (27). Findings that unopposed estrogens are inversely associated with breast cancer risk (28), but show strong positive relations for endometrial cancer (28, 29), provide additional support for differing etiologic roles of estrogens on the two cancer sites.

Especially high risks of endometrial cancer have been related to obesity (particularly for type I cancers), and it is widely accepted that this is partly due to higher levels of estrogens among obese postmenopausal women given peripheral conversion of androgens to estrogens in adipose tissue (30). Several investigations have explored the extent to which estrogens explain the effects of obesity on breast cancer risk (31, 32), with findings that the relations with obesity were attenuated and became nonsignificant after adjustment for estrogens, most notably estradiol. However, effects of estrogens on the obesity–endometrial cancer relation have been less well explored. We observed similar results as have been seen for breast cancer, namely, an attenuation of risks associated with obesity after adjustment for unconjugated estradiol levels. However, for endometrial cancer, where obesity is more strongly related to risk than it is for breast cancer, we were unable to completely eliminate the obesity-associated risks, suggesting that there may be other mediators of the association. Thus, further attention seems warranted on such factors as insulin, insulin-like growth factors, androgens, and inflammatory factors, which are also related to endometrial cancer risk as well as BMI (3, 4).

Much recent interest has focused on the etiologic heterogeneity of endometrial cancer, specifically whether there are differences between type I and II tumors. It has long been speculated that the numerically predominant type I tumors have hormonally driven etiologies (excess estrogen exposure) that develop from endometrial hyperplasias; in contrast, type II tumors are considered unrelated to typical endometrial cancer risk factors and endometrial hyperplasia (33). Risk factor differences, however, have only recently been robustly assessed in epidemiologic investigations. It has thus been of interest that these studies support risk factor differences, with accepted endometrial cancer risk factors (e.g., obesity, nulliparity, absence of cigarette smoking) being stronger for type I than II tumors (17, 18, 34–36). As an extension, it would be expected that the effects of endogenous estrogens would also be differential; however, apart from one small investigation (37), these relations have not been explored.

Although estrogens appeared to influence both type I and II tumors, our findings showed that the association of unconjugated estradiol was stronger for the type I tumors, consistent with a central role for estrogens in influencing the progression of endometrial hyperplasias to these malignancies (38). Although we did not observe the difference to be statistically significant, we also observed unconjugated estradiol more strongly linked to low-grade than high-grade tumors. This finding supports recent epidemiologic (17) as well as clinical (39) data suggesting that the high-grade endometrioid tumors may be etiologically distinct from other type I cancers and more resemble type II cancers.

This study had some notable strengths, as well as a few limitations. Strengths included the relatively large number of cases identified through a well-defined population for whom prediagnostic estrogen levels could be measured and adjusted for other important endometrial cancer risk factors. The assay used to measure estrogens and their metabolites has extremely high sensitivity and specificity. Nonetheless, many of the metabolites were highly correlated with each other, presenting problems for disentangling effects. In addition, despite the relatively large number of endometrial cases, few were diagnosed with type II tumors, limiting our ability to explore etiologic heterogeneity across tumor subtypes. We also included only postmenopausal women, conducted assays on a single serum sample collected at baseline, and did not measure sex hormone blinding globulin levels. Furthermore, estrogens were circulating measures, whereas more biologically meaningful assessments may derive from tissue assays, which are methodologically challenging (40).

In summary, our results support a central role for estrogens in endometrial cancer. Although the strongest effect was for unconjugated estradiol, other estrogens and estrogen metabolites may also contribute to risk. The association with unconjugated estradiol predominated for type I cancers, consistent with an important role for estrogenic influences in the progression of endometrial hyperplasia to cancer. Additional attention focused on estrogen metabolism in relation to other endometrial cancer biomarkers, and as measured in tissue, may further our understanding of endometrial carcinogenesis.

No potential conflicts of interest were disclosed.

Conception and design: L.A. Brinton, B.J. Fuhrman, N. Wentzensen

Development of methodology: L.A. Brinton, B. Trabert, R.T. Falk, B.J. Fuhrman

Acquisition of data (provided animals, acquired and managed patients, provided facilities, etc.): L.A. Brinton, G.L. Anderson, M.L. Gass, X. Xu

Analysis and interpretation of data (e.g., statistical analysis, biostatistics, computational analysis): L.A. Brinton, B. Trabert, R.T. Falk, L.H. Kuller, R.M. Pfeiffer, H.D. Strickler, N. Wentzensen

Writing, review, and/or revision of the manuscript: L.A. Brinton, B. Trabert, G.L. Anderson, R.T. Falk, A.S. Felix, B.J. Fuhrman, M.L. Gass, L.H. Kuller, R.M. Pfeiffer, T.E. Rohan, H.D. Strickler, X. Xu, N. Wentzensen

Administrative, technical, or material support (i.e., reporting or organizing data, constructing databases): L.A. Brinton, B. Trabert, B.J. Fuhrman

Study supervision: L.A. Brinton, B. Trabert

The authors acknowledge the following short list of WHI investigators:

Program Office: National Heart, Lung, and Blood Institute, Bethesda, Maryland (Jacques Rossouw, Shari Ludlam, Dale Burwen, Joan McGowan, Leslie Ford, and Nancy Geller).

Clinical Coordinating Center: Fred Hutchinson Cancer Research Center, Seattle, WA (Garnet Anderson, Ross Prentice, Andrea LaCroix, and Charles Kooperberg).

Investigators and Academic Centers: Brigham and Women's Hospital, Harvard Medical School, Boston, MA (JoAnn E. Manson); MedStar Health Research Institute/Howard University, Washington, DC (Barbara V. Howard); Stanford Prevention Research Center, Stanford, CA (Marcia L. Stefanick); The Ohio State University, Columbus, OH (Rebecca Jackson); University of Arizona, Tucson/Phoenix, AZ (Cynthia A. Thomson); University at Buffalo, Buffalo, NY (Jean Wactawski-Wende); University of Florida, Gainesville/Jacksonville, FL (Marian Limacher); University of Iowa, Iowa City/Davenport, IA (Robert Wallace); University of Pittsburgh, Pittsburgh, PA (Lewis Kuller); Wake Forest University School of Medicine, Winston-Salem, NC (Sally Shumaker).

Women's Health Initiative Memory Study: Wake Forest University School of Medicine, Winston-Salem, NC (Sally Shumaker).

For a list of all the investigators who have contributed to WHI science, please visit https://www.whi.org/researchers/Documents%20%20Write%20a%20Paper/WHI%20Investigator%20Long%20List.pdf.

This work was supported in part by the Intramural Research Program of the NCI. The WHI program is funded by the National Heart, Lung, and Blood Institute, NIH, U.S. Department of Health and Human Services through contracts HHSN268201100046C, HHSN268201100001C, HHSN268201100002C, HHSN268201100003C, HHSN268201100004C, and HHSN271201100004C.

1.
Kaaks
R
,
Lukanova
A
,
Kurzer
MS
. 
Obesity, endogenous hormones, and endometrial cancer risk: a synthetic review
.
Cancer Epidemiol Biomarkers Prev
2002
;
11
:
1531
43
.
2.
Brown
SB
,
Hankinson
SE
. 
Endogenous estrogens and the risk of breast, endometrial, and ovarian cancers
.
Steroids
2015
;
99
:
8
10
.
3.
Allen
NE
,
Key
TJ
,
Dossus
L
,
Rinaldi
S
,
Cust
A
,
Lukanova
A
, et al
Endogenous sex hormones and endometrial cancer risk in women in the European Prospective Investigation into Cancer and Nutrition (EPIC)
.
Endocr Relat Cancer
2008
;
15
:
485
97
.
4.
Gunter
MJ
,
Hoover
DR
,
Yu
H
,
Wassertheil-Smoller
S
,
Manson
JE
,
Li
J
, et al
A prospective evaluation of insulin and insulin-like growth factor-I as risk factors for endometrial cancer
.
Cancer Epidemiol Biomarkers Prev
2008
;
17
:
921
9
.
5.
Lukanova
A
,
Lundin
E
,
Micheli
A
,
Arslan
A
,
Ferrari
P
,
Rinaldi
S
, et al
Circulating levels of sex steroid hormones and risk of endometrial cancer in postmenopausal women
.
Int J Cancer
2004
;
108
:
425
32
.
6.
Zeleniuch-Jacquotte
A
,
Akhmedkhanov
A
,
Kato
I
,
Koenig
KL
,
Shore
RE
,
Kim
MY
, et al
Postmenopausal endogenous oestrogens and risk of endometrial cancer: results of a prospective study
.
Br J Cancer
2001
;
84
:
975
81
.
7.
Ziegler
RG
,
Fuhrman
BJ
,
Moore
SC
,
Matthews
CE
. 
Epidemiologic studies of estrogen metabolism and breast cancer
.
Steroids
2015
;
99
:
67
75
.
8.
Bradlow
HL
,
Sepkovic
DW
,
Klug
T
,
Osborne
MP
. 
Application of an improved ELISA assay to the analysis of urinary estrogen metabolites
.
Steroids
1998
;
63
:
406
13
.
9.
Fishman
J
,
Schneider
J
,
Hershcope
RJ
,
Bradlow
HL
. 
Increased estrogen-16 alpha-hydroxylase activity in women with breast and endometrial cancer
.
J Steroid Biochem
1984
;
20
:
1077
81
.
10.
Cavalieri
E
,
Chakravarti
D
,
Guttenplan
J
,
Hart
E
,
Ingle
J
,
Jankowiak
R
, et al
Catechol estrogen quinones as initiators of breast and other human cancers: implications for biomarkers of susceptibility and cancer prevention
.
Biochim Biophys Acta
2006
;
1766
:
63
78
.
11.
Dallal
CM
,
Tice
JA
,
Buist
DS
,
Bauer
DC
,
Lacey
JV
 Jr
,
Cauley
JA
, et al
Estrogen metabolism and breast cancer risk among postmenopausal women: a case-cohort study within B∼FIT
.
Carcinogenesis
2014
;
35
:
346
55
.
12.
Fuhrman
BJ
,
Schairer
C
,
Gail
MH
,
Boyd-Morin
J
,
Xu
X
,
Sue
LY
, et al
Estrogen metabolism and risk of breast cancer in postmenopausal women
.
J Natl Cancer Inst
2012
;
104
:
326
39
.
13.
Zeleniuch-Jacquotte
A
,
Shore
RE
,
Afanasyeva
Y
,
Lukanova
A
,
Sieri
S
,
Koenig
KL
, et al
Postmenopausal circulating levels of 2- and 16alpha-hydroxyestrone and risk of endometrial cancer
.
Br J Cancer
2011
;
105
:
1458
64
.
14.
Dallal
CM
,
Lacey
JV
 Jr
,
Pfeiffer
RM
,
Bauer
DC
,
Falk
RT
,
Buist
DS
, et al
Estrogen metabolism and risk of postmenopausal endometrial and ovarian cancer: the B approximately FIT Cohort
.
Horm Cancer
2016
;
7
:
49
64
.
15.
Audet-Walsh
E
,
Lepine
J
,
Gregoire
J
,
Plante
M
,
Caron
P
,
Tetu
B
, et al
Profiling of endogenous estrogens, their precursors, and metabolites in endometrial cancer patients: association with risk and relationship to clinical characteristics
.
J Clin Endocrinol Metab
2011
;
96
:
E330
9
.
16.
Zhao
H
,
Jiang
Y
,
Liu
Y
,
Yun
C
,
Li
L
. 
Endogenous estrogen metabolites as biomarkers for endometrial cancer via a novel method of liquid chromatography-mass spectrometry with hollow fiber liquid-phase microextraction
.
Horm Metab Res
2015
;
47
:
158
64
.
17.
Brinton
LA
,
Felix
AS
,
McMeekin
DS
,
Creasman
WT
,
Sherman
ME
,
Mutch
D
, et al
Etiologic heterogeneity in endometrial cancer: evidence from a Gynecologic Oncology Group trial
.
Gynecol Oncol
2013
;
129
:
277
84
.
18.
Setiawan
VW
,
Yang
HP
,
Pike
MC
,
McCann
SE
,
Yu
H
,
Xiang
YB
, et al
Type I and II endometrial cancers: have they different risk factors?
J Clin Oncol
2013
;
31
:
2607
18
.
19.
Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group
.
Control Clin Trials
1998
;
19
:
61
109
.
20.
Langer
RD
,
White
E
,
Lewis
CE
,
Kotchen
JM
,
Hendrix
SL
,
Trevisan
M
. 
The Women's Health Initiative Observational Study: baseline characteristics of participants and reliability of baseline measures
.
Ann Epidemiol
2003
;
13
:
S107
21
.
21.
Trabert
B
,
Brinton
LA
,
Anderson
GL
,
Pfeiffer
RM
,
Falk
RT
,
Strickler
HD
, et al
Circulating estrogens and postmenopausal ovarian cancer risk in the Women's Health Initiative Observational Study
.
Cancer Epidemiol Biomarkers Prev
2016
Feb 5. [Epub ahead of print].
22.
Xu
X
,
Roman
JM
,
Issaq
HJ
,
Keefer
LK
,
Veenstra
TD
,
Ziegler
RG
. 
Quantitative measurement of endogenous estrogens and estrogen metabolites in human serum by liquid chromatography-tandem mass spectrometry
.
Anal Chem
2007
;
79
:
7813
21
.
23.
Loud
JT.
Circulating estrogens and estrogens within the breast among postmenopausal BRCA1/2 mutation carriers
.
Breast Cancer Res Treat
2014
;
148
:
691
2
.
24.
Newbold
RR
,
Liehr
JG
. 
Induction of uterine adenocarcinoma in CD-1 mice by catechol estrogens
.
Cancer Res
2000
;
60
:
235
7
.
25.
Reddy
VV
,
Hanjani
P
,
Rajan
R
. 
Synthesis of catechol estrogens by human uterus and leiomyoma
.
Steroids
1981
;
37
:
195
203
.
26.
Zhu
BT
,
Conney
AH
. 
Functional role of estrogen metabolism in target cells: review and perspectives
.
Carcinogenesis
1998
;
19
:
1
27
.
27.
Takahashi
M
,
Shimomoto
T
,
Miyajima
K
,
Yoshida
M
,
Katashima
S
,
Uematsu
F
, et al
Effects of estrogens and metabolites on endometrial carcinogenesis in young adult mice initiated with N-ethyl-N′-nitro-N-nitrosoguanidine
.
Cancer Lett
2004
;
211
:
1
9
.
28.
Anderson
GL
,
Chlebowski
RT
,
Aragaki
AK
,
Kuller
LH
,
Manson
JE
,
Gass
M
, et al
Conjugated equine oestrogen and breast cancer incidence and mortality in postmenopausal women with hysterectomy: extended follow-up of the Women's Health Initiative randomised placebo-controlled trial
.
Lancet Oncol
2012
;
13
:
476
86
.
29.
Trabert
B
,
Wentzensen
N
,
Yang
HP
,
Sherman
ME
,
Hollenbeck
AR
,
Park
Y
, et al
Is estrogen plus progestin menopausal hormone therapy safe with respect to endometrial cancer risk?
Int J Cancer
2013
;
132
:
417
26
.
30.
Siiteri
PK
. 
Adipose tissue as a source of hormones
.
Am J Clin Nutr
1987
;
45
:
277
82
.
31.
Key
TJ
,
Appleby
PN
,
Reeves
GK
,
Roddam
A
,
Dorgan
JF
,
Longcope
C
, et al
Body mass index, serum sex hormones, and breast cancer risk in postmenopausal women
.
J Natl Cancer Inst
2003
;
95
:
1218
26
.
32.
Rinaldi
S
,
Key
TJ
,
Peeters
PH
,
Lahmann
PH
,
Lukanova
A
,
Dossus
L
, et al
Anthropometric measures, endogenous sex steroids and breast cancer risk in postmenopausal women: a study within the EPIC cohort
.
Int J Cancer
2006
;
118
:
2832
9
.
33.
Bokhman
JV
. 
Two pathogenetic types of endometrial carcinoma
.
Gynecol Oncol
1983
;
15
:
10
7
.
34.
Felix
AS
,
Weissfeld
JL
,
Stone
RA
,
Bowser
R
,
Chivukula
M
,
Edwards
RP
, et al
Factors associated with Type I and Type II endometrial cancer
.
Cancer Causes Control
2010
;
21
:
1851
6
.
35.
McCullough
ML
,
Patel
AV
,
Patel
R
,
Rodriguez
C
,
Feigelson
HS
,
Bandera
EV
, et al
Body mass and endometrial cancer risk by hormone replacement therapy and cancer subtype
.
Cancer Epidemiol Biomarkers Prev
2008
;
17
:
73
9
.
36.
Yang
HP
,
Wentzensen
N
,
Trabert
B
,
Gierach
GL
,
Felix
AS
,
Gunter
MJ
, et al
Endometrial cancer risk factors by 2 main histologic subtypes: the NIH-AARP Diet and Health Study
.
Am J Epidemiol
2013
;
177
:
142
51
.
37.
Sherman
ME
,
Sturgeon
S
,
Brinton
LA
,
Potischman
N
,
Kurman
RJ
,
Berman
ML
, et al
Risk factors and hormone levels in patients with serous and endometrioid uterine carcinomas
.
Mod Pathol
1997
;
10
:
963
8
.
38.
Sherman
ME
. 
Theories of endometrial carcinogenesis: a multidisciplinary approach
.
Mod Pathol
2000
;
13
:
295
308
.
39.
Zannoni
GF
,
Vellone
VG
,
Arena
V
,
Prisco
MG
,
Scambia
G
,
Carbone
A
, et al
Does high-grade endometrioid carcinoma (grade 3 FIGO) belong to type I or type II endometrial cancer? A clinical-pathological and immunohistochemical study
.
Virchows Arch
2010
;
457
:
27
34
.
40.
Stanczyk
FZ
,
Mathews
BW
,
Sherman
ME
. 
Relationships of sex steroid hormone levels in benign and cancerous breast tissue and blood: a critical appraisal of current science
.
Steroids
2015
;
99
:
91
102
.