This review synthesized and appraised the evidence for an effect of inflammation on breast cancer risk. Systematic searches identified prospective cohort and Mendelian randomization studies relevant to this review. Meta-analysis of 13 biomarkers of inflammation were conducted to appraise the evidence for an effect breast cancer risk; we examined the dose–response of these associations. Risk of bias was evaluated using the ROBINS-E tool and the quality of evidence was appraised with Grading of Recommendations Assessment, Development, and Evaluation. Thirty-four observational studies and three Mendelian randomization studies were included. Meta-analysis suggested that women with the highest levels of C-reactive protein (CRP) had a higher risk of developing breast cancer [risk ratio (RR) = 1.13; 95% confidence interval (CI), 1.01–1.26] compared with women with the lowest levels. Women with highest levels of adipokines, particularly adiponectin (RR = 0.76; 95% CI, 0.61–0.91) had a reduced breast cancer risk, although this finding was not supported by Mendelian randomization analysis. There was little evidence of an effect of cytokines, including TNFα and IL6, on breast cancer risk. The quality of evidence for each biomarker ranged from very low to moderate. Beyond CRP, the published data do not clearly support the role of inflammation in the development of breast cancer.

Observational evidence suggests that physical activity has a protective effect on breast cancer risk (1, 2). The underlying mechanisms are yet to be clarified but may involve inflammation (1, 2). However, the certainty of a physical activity — inflammation — breast cancer pathway cannot be established without systematic synthesis and appraisal of the evidence for an effect of inflammation on breast cancer risk.

Our current understanding of the role of inflammation in carcinogenesis is underpinned by evidence from in vivo and ex vivo studies that implicate inflammatory biomarkers in all stages of tumor development (3). Inflammatory signals induce an elevation of mutagenic reactive oxygen species which cause cellular oxidative stress and DNA damage (4). Genomic instability allows budding tumor cells to acquire mutations, while a competent immune system places pressure on cells to keep mutations that favor survival (5). As cancer cells proliferate, the secretion of cytokines facilitates cancer cell growth and angiogenesis (6).

Some observational studies suggest that increased levels of circulating inflammatory biomarkers may increase breast cancer risk (7). C-reactive protein (CRP), a commonly measured, nonspecific biomarker of inflammation, is the biomarker that has been most frequently studied in the context of breast cancer development (8). Some observational studies have also reported that long-term users of NSAIDs have a reduced risk of breast cancer (9). Increased inflammatory changes in previously healthy breast tissue are also associated with breast cancer risk (10). While existing systematic reviews on CRP and breast cancer risk have generally found positive associations (8, 11), other inflammatory biomarkers and breast cancer development have not been carefully studied. Kehm and colleagues recently conducted a systematic review of inflammatory biomarkers and breast cancer risk but concluded that evidence from markers other than CRP is limited (7).

Despite a compelling biological hypothesis and evidence for immunomodulatory effects induced by physical activity (12), epidemiologic findings on the role of circulating inflammatory biomarkers on breast cancer risk have not been rigorously evaluated. This review uses the World Cancer Research Fund (WCRF) International and University of Bristol causal evidence synthesis framework for conducting systematic reviews of mechanistic pathways for exposure–cancer associations (1). Our previous systematic reviews addressed the impact of physical activity on the sex steroid hormone (13, 14) and insulin signaling pathways (15, 16) and how these effects may alter breast cancer risk. The first part of this two-part systematic review investigated the impact of physical activity on the production of inflammatory biomarkers (12). Here, we synthesize and appraise the evidence that circulating inflammatory biomarkers affect breast cancer risk.

Details on the methods for this review have been published in a protocol paper (1) and registered on PROSPERO (CRD42020165689). Briefly, systematic searches for keywords and Medical Subject Headings were conducted in MEDLINE (Ovid) and EMBASE (Ovid) until 23 February 2021. The search strategy can be found in Supplementary Methods and Materials (Supplementary Table S1). Eligible studies had a prospective design and examined the association between at least one inflammatory biomarker and breast cancer incidence. Studies conducted in a cohort of patients with a diagnosed medical condition (such as allergy and autoimmune conditions) were excluded. Study participants were required to be post-menarche. The inflammatory biomarkers of interest were previously identified and reported in our protocol paper (1). These were CRP, TNFα, leptin, adiponectin, IL1, IL1β, IL6, IL8, IL10, IL13, IFNγ, chemokine ligand 2 (CCL2), and prostaglandins.

Two authors (M.W.C. Lou and A.E. Drummond) independently screened the titles and abstracts; where there was consensus that studies were not relevant, they were excluded. Two authors (M.W.C. Lou and A.E. Drummond) then reviewed the full text of remaining papers; studies were included on the basis of consensus. Data were extracted into pre-piloted tables and summarized descriptively. For biomarkers with results reported from at least three separate studies (excluding Mendelian randomization studies), random-effects meta-analysis was conducted to estimate the effect size (risk ratio) for the highest category of biomarker compared with the lowest category. Multiple estimates from the same study were included in the same meta-analysis where it was clear that samples did not overlap. Where heterogeneity was identified, a sub-group analysis on the effect size by menopausal status at baseline was conducted. Sensitivity analyses were also completed to assess study estimate differences by exogenous hormone use (i.e., oral-contraceptive use or hormonal replacement therapy). Where it was not indicated that hormone use was controlled for either in statistical analysis or by sample restriction, the study was left out of the sensitivity analysis. A one-stage, dose–response meta-analysis of summarized data using restricted cubic splines was performed (17). The Risk of Bias in Nonrandomized Studies-of-Exposures (ROBINS-E; ref. 18) tool was used to evaluate risk of bias (ROB) for the observational studies. The ROBINS-E tool was not developed to assess Mendelian randomization studies. There is currently no validated tool to assess ROB in Mendelian randomization studies. The overall quality of evidence and strength of the findings were assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) system (19). All statistical analyses were performed using Stata version 16 (Stata Corporation, College Station, Texas).

Search results

The search results are presented in Fig. 1. Of the 11,316 publications retrieved in the search, 37 investigated the effect of inflammatory biomarkers on breast cancer risk. Of these, 34 publications were observational studies (26 independent cohorts; refs. 11, 20–50, 51, 52), and 3 publications were two-sample Mendelian randomization analyses using summary-level data (53–55). The Mendelian randomization publications used SNPs that predicted a proportion of circulating inflammatory markers in UK Biobank Study (UKBB; ref. 55) participants as instrumental variables for the biomarkers of interest. These genetic proxies were used as the exposures of interest in analyses of breast cancer cases and controls from a large, international consortium (BCAC; refs. 53–55). Both studies predominantly included people of European ancestry.

Figure 1.

PRISMA flow diagram. This figure incorporates literature search, screening and study selection.

Figure 1.

PRISMA flow diagram. This figure incorporates literature search, screening and study selection.

Close modal

Study characteristics

Characteristics of the included studies are detailed in the Supplementary Methods and Materials (Supplementary Tables S2A and S2B). Follow-up time in eligible studies ranged from less than one year to 25 years. All observational studies included postmenopausal women at baseline blood collection (n = 26 independent studies; 34 publications), with 16 of these also including premenopausal women (18 publications; refs. 20, 21, 26, 28, 29, 34, 38, 41–43, 46–50, 11, 51, 52). The sample size of studies ranged between 142 to 7,938 for premenopausal women and 302 to 44,715 for postmenopausal women. Inflammatory biomarkers examined in the studies included blood concentrations of CRP (n = 17; refs. 11, 20–22, 24, 28–30, 33, 35, 39–42, 44, 46, 48–52), TNFα (n = 4; refs. 20, 27, 33, 38), leptin (n = 9; refs. 20, 26, 32–34, 40, 43, 45, 47), adiponectin (n = 9; refs. 20, 26, 30, 31, 33, 40, 47, 48), IL6 (n = 4; refs. 20, 27, 33, 35), IL8 (n = 1; ref. 27), IL1β (n = 1; ref. 27), CCL2 (n = 2; refs. 43, 47) and urinary prostaglandin E2 (PGE2) metabolites (n = 3; refs. 36, 37). The Mendelian randomization studies were performed on two-sample, summary-level data. The sample sizes for the outcome studies were 298,951 (BCAC; refs. 53–55) and 367,643 (UKBB; ref. 55). One Mendelian randomization study was available for each of CRP (54), TNFα (55), adiponectin (54), IL6 (54), IL13 (53), and CCL2 (53).

ROB

ROB assessments are presented in the Supplementary Methods and Materials (Supplementary Table S3). All observational studies had at least moderate ROB, due to the potential for uncontrolled or residual confounding. Assessment results found one serious (49) and 31 moderate (11, 20–48, 50–52) ROB observational studies. The study with serious ROB did not control for confounding arising from adiposity, alcohol, or diet, and did not provide an explanation for not doing so (49). All other observational studies adjusted for age and body mass index (BMI; or another proxy for adiposity). Diet and/or alcohol were not controlled for in several studies (24–26, 34, 35, 38, 42, 45), with a few indicating that adjustments for these factors did not change risk estimates (29, 31, 39–41, 44). ROB in exposure classification was low for most studies, though it was deemed moderate for studies with high (>15% variation; ref. 56) or missing information on intra- and inter-assay variation (21, 24, 27, 38, 41, 44, 52) and poor sensitivity (limits of detection, biomarker-dependent; refs. 49, 51). The three Mendelian randomization studies had potential bias arising from weak genetic instruments and horizontal pleiotropy, although two studies had employed sensitivity analyses to test results in the presence of potential bias (53, 54).

Effect of inflammatory biomarkers on breast cancer risk

Meta-analysis results for each inflammatory biomarker are presented as forest plots and can be found in Figs. 2 and 3 for overall risk of breast cancer, and Supplementary Methods and Materials (Supplementary Figs. S1–S5) for subgroup and sensitivity analyses. Where categorical data were available, estimates compared the highest category level of the biomarker to the lowest category level. Dose–response curves for overall breast cancer risk are presented in Fig. 4 (CRP, leptin, adiponectin) and by menopausal subgroups in Supplementary Methods and Materials (Supplementary Figs. S1D, S4C, and S5C).

Figure 2.

Forest plots for effects of inflammatory biomarkers on breast cancer risk. Forest plots for (A) CRP, (B) TNFα, and (C) IL6.

Figure 2.

Forest plots for effects of inflammatory biomarkers on breast cancer risk. Forest plots for (A) CRP, (B) TNFα, and (C) IL6.

Close modal
Figure 3.

Forest plots for effects of inflammatory biomarkers on breast cancer risk. Forest plots for (A) leptin and (B) adiponectin.

Figure 3.

Forest plots for effects of inflammatory biomarkers on breast cancer risk. Forest plots for (A) leptin and (B) adiponectin.

Close modal
Figure 4.

Dose–response curves for effects of inflammatory biomarkers on breast cancer risk. Dose–response curves for (A) CRP, (B) leptin, and (C) adiponectin.

Figure 4.

Dose–response curves for effects of inflammatory biomarkers on breast cancer risk. Dose–response curves for (A) CRP, (B) leptin, and (C) adiponectin.

Close modal

CRP

CRP was associated with an increased risk of breast cancer for women with the highest levels of CRP compared with the lowest levels [n = 16; risk ratio (RR) = 1.13; 95% confidence interval (CI), 1.01–1.26; I2 = 34.87%; Fig. 2). The CRP-breast cancer relationship appeared to be dose-dependent, with a potential inverse U relationship (Fig. 4). In a sub-group analysis, there was little evidence of an effect in premenopausal women (n = 6; RR = 1.02; 95% CI, 0.84–1.21; I2 = 0%; Supplementary Methods and Materials; Fig. 1A). For postmenopausal women, CRP was positively associated with an increased risk of breast cancer for the highest category compared with the lowest (n = 14; RR = 1.16; 95% CI, 0.98–1.34; I2 = 44.12%), though the estimate was imprecisely estimated (Supplementary Methods and Materials; Fig. 1A). The Mendelian randomization study did not find evidence for an effect of CRP on breast cancer risk (OR per 1-SD increase = 1.03; 95% CI, 0.94–1.13; P = 0.48); no difference was reported between ER+ and ER- breast cancers (54). Of the 15 studies that measured CRP, 12 used measures for high-sensitivity CRP (hsCRP) or had a lower limit of detection of at least 0.3 mg/L (11, 20–22, 24, 28, 29, 41, 44, 46, 47, 50). Sensitivity analyses excluding studies with unknown status for exogenous hormone use (Supplementary Methods and Materials; Fig. 1B), or studies with high ROB (Supplementary Methods and Materials; Fig. 1C), did not substantially change the RR or heterogeneity estimate.

TNFα

Meta-analysis suggested that the highest category of TNFα compared with the lowest category was associated with a possible decreased risk of breast cancer (n = 4; RR = 0.84; 95% CI, 0.57–1.10; I2 = 24.3%; Fig. 2). Subgroup analysis could not explain the heterogeneity, as this remained high for each subgroup including pre- (I2 = 70%) and postmenopausal women (I2 = 89%; Supplementary Methods and Materials; Fig. 2A). Sensitivity analyses excluding studies with unknown status for exogenous hormone use (Supplementary Methods and Materials; Fig. 2B) did not substantially change the risk estimate or heterogeneity estimate. Consistent with the meta-analysis, a Mendelian randomization study found strong evidence that TNFα decreased breast cancer risk (OR per 1-SD increase = 0.51; 95% CI, 0.39–0.67; ref. 55).

Interleukins

The only interleukin with sufficient studies (n = 3) to conduct a meta-analysis was IL6. We found little evidence of an association with breast cancer risk (RR = 1.04; 95% CI, 0.66–1.42; I2 = 35.05%; Fig. 2). There was insufficient evidence to determine any differences by menopause subgroup (Supplementary Methods and Materials; Fig. 3A). A Mendelian randomization study found some evidence of a positive causal effect (OR per 1-SD increase = 1.09; 95% CI, 0.96–1.25; ref. 54).

In an individual Mendelian randomization study, higher levels of IL13 led to a small increase in breast cancer risk in another (OR per 1-SD increase = 1.06; 95% CI, 1.03–1.10; ref. 53). In a nested case–control study, there was a small increase in postmenopausal breast cancer risk was noted for increasing levels of IL8 (OR highest versus lowest category = 1.09; 95% CI, 0.71–1.66), though estimates were imprecisely estimated as confidence intervals (CI) were wide (27).

Leptin

Following meta-analysis, women with the highest levels of leptin were not clearly more likely to develop breast cancer compared with women with the lowest levels (n = 8; RR = 0.90; 95% CI, 0.63–1.18; I2 = 70.1%; Fig. 3). There was no evidence of a dose–response relationship (Fig. 4).

Subgroup analysis suggested a possible difference in breast cancer risk for pre- and postmenopausal levels of circulating leptin. For premenopausal women, a meta-analysis found that those with the highest levels compared with the lowest had decreased breast cancer risk (n = 4; RR = 0.56; 95% CI, 0.39–0.72; I2 = 0.0%; Supplementary Methods and Materials; Fig. 4A). Conversely, for postmenopausal women, higher levels of leptin may have been associated with increased breast cancer risk (n = 7; RR = 1.23; 95% CI, 0.86–1.60; I2 = 46.8%). However, there was moderate heterogeneity and a wide CI, limiting the certainty of this result. In a sensitivity analysis excluding studies with unknown status for exogenous hormone use, the positive association in postmenopausal women was strengthened, with a large reduction in heterogeneity (n = 5; RR = 1.37; 95% CI, 1.06–1.67; I2 = 0.0%; Supplementary Methods and Materials; Fig. 4B).

Adiponectin

Women with the highest levels of adiponectin experienced a decreased risk in overall breast cancer risk (n = 8; RR = 0.76; 95% CI, 0.61–0.91; I2 = 37.02%), compared with those with the lowest levels (Fig. 3). A sensitivity analysis excluding studies with unknown status for exogenous hormone use minimally changed the risk estimate (n = 7; RR = 0.72; 95% CI, 0.56–0.87; I2 = 38.4%; Supplementary Methods and Materials; Fig. 5B). Sub-group analyses revealed that adiponectin is protective for postmenopausal women (n = 3; RR = 0.75; 95% CI, 0.57–0.92; I2 = 47.0%; Supplementary Methods and Materials; Fig. 5A), and showed evidence of a dose–response effect (Supplementary Methods and Materials; Fig. 5C). There was little evidence of an association for premenopausal women, with high heterogeneity (RR = 0.93; 95% CI, 0.44–1.41; I2 = 52.4%). A Mendelian randomization study did not support a causal effect of adiponectin on breast cancer risk (OR per 1-SD increase = 1.06; 95% CI, 0.81–1.40), with wide and overlapping CIs from the meta-analysis (54).

Prostaglandins

Three studies examined prostaglandins and breast cancer risk. Urinary metabolite of PGE2 was positively associated with postmenopausal breast cancer (HR for highest versus lowest category = 2.01; 95% CI, 1.01–4.29) in one study (36). A second study observed similar results with a dose–response relationship only for the subgroup with BMI < 25 (25). Urinary prostaglandin F2-α metabolite was not associated with breast cancer risk in a third study (23).

Other cytokines

In individual studies, there was contrasting evidence of an effect of CCL2. Observational studies did not clearly support an increased risk for higher compared with lower levels of CCL2 and breast cancer risk; (OR = 1.14; 95% CI, 0.70–1.85; ref. 47) and (OR = 1.01; 95% CI, 0.48–1.74; ref. 43). In contrast, in a Mendelian randomization study genetically predicted circulating levels of CCL2 increased overall breast cancer risk (OR per 1-SD increase = 1.08; 95% CI, 1.03–1.12; ref. 53).

Table 1 presents results of the GRADE appraisal for biomarkers where there were sufficient studies to conduct a meta-analysis. Initially, the evidence for all inflammatory biomarkers and breast cancer risk was graded as low, as the results were based on observational studies only. The quality of evidence for CRP and breast cancer risk was upgraded to moderate due to evidence of a dose–response relationship. Evidence for TNFα and breast cancer risk was also upgraded as moderate due to the triangulation of evidence, with consistency in direction of effect between observational and Mendelian randomization studies. The quality of evidence for IL6 was downgraded to very low due to imprecision and inconsistency in the available evidence of only 3 studies. The quality of evidence for adiponectin was graded up due to a large magnitude of effect.

Table 1.

GRADE appraisal for inflammatory biomarkers – breast cancer pathways.

Inflammatory biomarkerStudy type, number, sample sizeMeta-analysis effect estimates (RR, 95% CI)Dose–responseQuality of evidence
CRP  
Overall Observational, 16 (153,669) 1.13 (1.01–1.26) Inverted U  
 Mendelian randomization, 1 (228,951) 1.03 (0.94–1.13)  Moderatea 
TNFα  
Overall Observational, 4 (2,256) 0.84 (0.57–1.10) N/A  
 Mendelian randomization, 1 (596,594) 0.51 (0.39–0.67)  Moderateb 
IL6  
Overall Observational, 3 (2,152) 1.04 (0.66–1.42) N/A  
 Mendelian randomization, 1 (228,951) 1.09 (0.96–1.25)  Very lowc 
Leptin  
Overall Observational, 8 (4,291) 0.90 (0.63–1.18) None Low 
Adiponectin  
Overall Observational, 8 (4,763) 0.76 (0.61–0.91) Linear  
 Mendelian randomization, 1 (228,951) 1.06 (0.81–1.40)  Moderated 
Inflammatory biomarkerStudy type, number, sample sizeMeta-analysis effect estimates (RR, 95% CI)Dose–responseQuality of evidence
CRP  
Overall Observational, 16 (153,669) 1.13 (1.01–1.26) Inverted U  
 Mendelian randomization, 1 (228,951) 1.03 (0.94–1.13)  Moderatea 
TNFα  
Overall Observational, 4 (2,256) 0.84 (0.57–1.10) N/A  
 Mendelian randomization, 1 (596,594) 0.51 (0.39–0.67)  Moderateb 
IL6  
Overall Observational, 3 (2,152) 1.04 (0.66–1.42) N/A  
 Mendelian randomization, 1 (228,951) 1.09 (0.96–1.25)  Very lowc 
Leptin  
Overall Observational, 8 (4,291) 0.90 (0.63–1.18) None Low 
Adiponectin  
Overall Observational, 8 (4,763) 0.76 (0.61–0.91) Linear  
 Mendelian randomization, 1 (228,951) 1.06 (0.81–1.40)  Moderated 

RRs summarize effects comparing the highest versus lowest category of blood biomarker concentration. Mendelian randomization effect estimate represents the OR per standard deviation increase in the exposure.

aGraded up due to dose–response effect in observational studies (Fig. 4A).

bGraded up due to triangulation of evidence.

cGraded down due to imprecision and inconsistency in the available evidence.

dGraded up due to substantial magnitude of effect.

In our review of inflammation and breast cancer risk, only increases in CRP were shown to increase breast cancer risk. A possible decrease in breast cancer risk was seen for higher levels of TNFα, leptin and adiponectin; however, wide CIs and heterogeneity limited the certainty of these findings. There was no clear evidence of a relationship between IL6 and breast cancer risk. Evidence was graded as very low (IL6), low (CRP, TNFα, leptin), or moderate (adiponectin).

The robust methodology used to search, synthesize, and appraise the current evidence on inflammatory biomarkers and breast cancer risk is a key strength of our review. The prespecified list of biomarkers in our search strategy improved identification of relevant articles compared with a previous review (7). We have identified five additional studies to the most recent meta-analysis of CRP and breast cancer risk (8), and additional previously unreviewed studies on cytokines (41, 43). Furthermore, only prospective studies and Mendelian randomization studies were included. Given that these study designs have their own strengths and limitations, incorporating findings from both enabled us to triangulate evidence (where risk estimates which align in direction may indicate stronger evidence of a true effect; ref. 57). Unlike observational studies that are inevitably subject to residual confounding, Mendelian randomization studies harness the randomization of genetic assignment at conception to measure causal effects between genetic proxies and the outcome, akin to a trial. In our review, triangulation of evidence was observed for TNFα, where higher levels were associated with decreased breast cancer risk in both a meta-analysis of observational studies and a Mendelian randomization study.

This systematic review revealed a sparsity of evidence from prospective cohorts and Mendelian randomization studies. Of the 13 biomarkers searched, publications included in the review examined 10, and only five biomarkers met criteria to facilitate a meta-analysis. Studies that measured biomarkers in premenopausal women were limited (17 of the 34 publications). Given that risk factors and mechanisms for breast cancer development likely differ between pre- and postmenopausal women (2, 58), and that ovulation itself appears to parallel with inflammation (59), more evidence is required to further clarify mechanisms in premenopausal women.

There was moderate to high heterogeneity noted for all meta-analyses. Subgroup meta-analyses were conducted to assess any potential differences by menopausal status. While menopause explained some of the heterogeneity for leptin, the sources of heterogeneity could not be further clarified for other markers due to the limited reporting of stratified results and inconsistent control for confounders between studies.

Risk factors contributing to breast cancer may differ by disease subtypes (60). However, few studies reported results by hormone receptor (HR) status and/or molecular subgroups. Of the studies that did investigate results by HR status, no significant difference was found in most observational studies (26, 33, 34, 52). One study found CRP to be associated with HR-negative breast cancers only (46). Mendelian randomization studies found CCL2 to be associated with overall and HR+ breast cancer (53), IL13 with both HR+ and HR- (53), and no significant differences for CRP, TNFα, adiponectin, and IL6 (54, 55).

Exogenous hormone use was mostly well described in studies and was adjusted for in statistical analyses, as is typical in studies on breast cancer. We included women who were taking exogenous hormones in our main analyses, although sensitivity analyses removed these and findings remained consistent. In contrast, the use of NSAIDs or aspirin was not routinely reported or adjusted for. This may be because NSAID and aspirin use is more difficult to measure, and use is typically occasional. Anti-inflammatory medication may pose a potential source of confounding in the prospective cohort studies. A recent meta-analysis of randomized controlled trials suggested that use of low-dose aspirin may offer a small degree of protection against breast cancer (61).

Almost all studies measured biomarkers only once at baseline. Correspondingly, exposure measurements were potentially limited by non-differential misclassification, leading to a potential underestimation of effects. Sensitivity analyses excluding cases diagnosed within 12/24 months of blood draw were not consistently reported amongst studies. However, no significant differences in risk estimates were observed in studies that conducted sensitivity analyses investigate risk with a time-lag until diagnosis (51, 52). Funnel plots of the included studies indicated that smaller studies with null or weak associations may be missing for CRP, leptin, and adiponectin.

Prior narrative reviews suggest that inflammation increases cancer risk (3, 62). Chronic systemic inflammation may increase breast cancer risk by promoting continuous tissue remodeling and creating a tumorigenic environment in breast tissue (6, 63). For example, CRP is an acute-phase protein produced in the liver in response to pro-inflammatory signals from cytokines such as TNFα and IL6, and moderately high CRP is indicative of low-grade inflammation (64). Higher adiponectin is observed in more active people and those with lower adiposity, and is typically associated with decreased inflammation (65, 66). While our meta-analysis of prospective cohort studies supported the protective role of increased adiponectin, results from the Mendelian randomization study did not support a causal effect of adiponectin on breast cancer risk.

The results for TNFα were not anticipated, as increased levels of the pro-inflammatory biomarker appeared to decrease risk of breast cancer. These findings should be interpreted with caution due to the small number of studies (n = 4), and it may reflect the complex dual roles of TNFα in both its antitumor functions and inflammatory tumor-promoting functions (67). Results for leptin were also not expected as it is hypothesized to promote breast cancer through increasing circulating hormone levels via aromatization of androgens to estrogens (65). Leptin was associated with increased risk in postmenopausal women but decreased risk in premenopausal women. Interestingly, these effects were analogous to the associations between adiposity and pre- and postmenopausal breast cancer (2). While all studies examining leptin controlled for BMI, it is possible that residual confounding due to inadequate control for adiposity could explain the observed relationship.

The overarching aim of this two-part series of reviews was to determine whether the inflammation mediates the inverse relationship between physical activity and breast cancer risk. Although Part 1 identified decreases in CRP, TNFα, IL6, and leptin following exercise interventions (8), in Part 2 (this manuscript) only CRP was associated with increased breast cancer risk. While both the quality of evidence identified as well as the complex nature of inflammation should caution against simple conclusions, overall, these two reviews do not provide clear evidence for a physical activity – inflammation – breast cancer pathway. This does not eliminate the possibility of this pathway; however better-quality, large-scale studies are required clarify the evidence. Future prospective studies should investigate a wider range of biomarkers of inflammation, obtaining samples from both pre- and postmenopausal women.

C.T.V. Swain reports grants from World Cancer Research Fund (WCRF) during the conduct of the study. R.L. Milne reports grants from WCRF during the conduct of the study. D.R. English reports grants from WCRF during the conduct of the study. K.A. Brown reports grants from NIH/NCI outside the submitted work. T.R. Gaunt reports grants from UK Medical Research Council during the conduct of the study; grants from Biogen outside the submitted work. R.M. Martin reports grants from Cancer Research UK during the conduct of the study. B.M. Lynch reports grants from Wereld Kanker Onderzoek Fonds (WKOF); and grants from Victorian Cancer Agency during the conduct of the study. No disclosures were reported by the other authors.

Funding (IIG_2018_1732) was obtained from WKOF, as part of the WCRF International Grant Programme. K.A. Brown is supported by NIH/NCI R01 CA215797. EHvR is funded by the WKOF, as part of the WCRF International Grant Programme (grant no. 2016/1620). R.M. Martin is a National Institute for Health Research Senior Investigator (NIHR202411). R.M. Martin and S.J. Lewis were supported by the NIHR Biomedical Research Centre at University Hospitals Bristol and Weston NHS Foundation Trust and the University of Bristol and by a Cancer Research UK (C18281/A29019) Programme Grant (the Integrative Cancer Epidemiology Programme). B.M. Lynch was supported by a Fellowship from the Victorian Cancer Agency (MCRF18005).

The publication costs of this article were defrayed in part by the payment of publication fees. Therefore, and solely to indicate this fact, this article is hereby marked “advertisement” in accordance with 18 USC section 1734.

Note: Supplementary data for this article are available at Cancer Epidemiology, Biomarkers & Prevention Online (http://cebp.aacrjournals.org/).

1.
Lynch
BM
,
Milne
RL
,
English
DR
,
Brown
KA
,
Drummond
AE
,
Swain
CTV
, et al
.
Linking physical activity to breast cancer: text mining results and a protocol for systematically reviewing three potential mechanistic pathways
.
Cancer Epidemiol Biomarkers Prev
2022
;
31
:
11
15
.
2.
Chan
DSM
,
Abar
L
,
Cariolou
M
,
Nanu
N
,
Greenwood
DC
,
Bandera
EV
, et al
.
World cancer research fund international: continuous update project-systematic literature review and meta-analysis of observational cohort studies on physical activity, sedentary behavior, adiposity, and weight change and breast cancer risk
.
Cancer Causes Control
2019
;
30
:
1183
200
.
3.
Greten
FR
,
Grivennikov
SI
.
Inflammation and cancer: triggers, mechanisms, and consequences
.
Immunity
2019
;
51
:
27
41
.
4.
Liou
GY
,
Storz
P
.
Reactive oxygen species in cancer
.
Free Radic Res
2010
;
44
:
479
96
.
5.
Chow
MT
,
Moller
A
,
Smyth
MJ
.
Inflammation and immune surveillance in cancer
.
Semin Cancer Biol
2012
;
22
:
23
32
.
6.
Deshmukh
SK
,
Srivastava
SK
,
Poosarla
T
,
Dyess
DL
,
Holliday
NP
,
Singh
AP
, et al
.
Inflammation, immunosuppressive microenvironment and breast cancer: opportunities for cancer prevention and therapy
.
Ann Transl Med
2019
;
7
:
593
.
7.
Kehm
RD
,
McDonald
JA
,
Fenton
SE
,
Kavanaugh-Lynch
M
,
Leung
KA
,
McKenzie
KE
, et al
.
Inflammatory biomarkers and breast cancer risk: a systematic review of the evidence and future potential for intervention research
.
Int J Environ Res Public Health
2020
;
17
:
5445
.
8.
Chan
DS
,
Bandera
EV
,
Greenwood
DC
,
Norat
T
.
Circulating c-reactive protein and breast cancer risk-systematic literature review and meta-analysis of prospective cohort studies
.
Cancer Epidemiol Biomarkers Prev
2015
;
24
:
1439
49
.
9.
de Pedro
M
,
Baeza
S
,
Escudero
MT
,
Dierssen-Sotos
T
,
Gomez-Acebo
I
,
Pollan
M
, et al
.
Effect of cox-2 inhibitors and other nonsteroidal inflammatory drugs on breast cancer risk: a meta-analysis
.
Breast Cancer Res Treat
2015
;
149
:
525
36
.
10.
Danforth
DN
.
The role of chronic inflammation in the development of breast cancer
.
Cancers
2021
;
13
:
3918
.
11.
Wang
J
,
Lee
IM
,
Tworoger
SS
,
Buring
JE
,
Ridker
PM
,
Rosner
B
, et al
.
Plasma c-reactive protein and risk of breast cancer in two prospective studies and a meta-analysis
.
Cancer Epidemiol Biomarkers Prev
2015
;
24
:
1199
206
.
12.
Swain
CTV
,
Drummond
AE
,
Milne
RL
,
English
DR
,
Brown
KA
,
Lou
MWC
, et al
.
Linking physical activity to breast cancer risk via inflammation, part 1: the effect of physical activity on inflammation
.
Cancer Epidemiol Biomarkers Prev
2023
;
32
:
588
96
.
13.
Swain
CTV
,
Drummond
AE
,
Boing
L
,
Milne
RL
,
English
DR
,
Brown
KA
, et al
.
Linking physical activity to breast cancer via sex hormones, part 1: the effect of physical activity on sex steroid hormones
.
Cancer Epidemiol Biomarkers Prev
2022
;
31
:
16
27
.
14.
Drummond
AE
,
Swain
CTV
,
Brown
KA
,
Dixon-Suen
SC
,
Boing
L
,
van Roekel
EH
, et al
.
Linking physical activity to breast cancer via sex steroid hormones, part 2: the effect of sex steroid hormones on breast cancer risk
.
Cancer Epidemiol Biomarkers Prev
2022
;
31
:
28
37
.
15.
Swain
CTV
,
Drummond
AE
,
Milne
RL
,
English
DR
,
Brown
KA
,
Chong
JE
, et al
.
Linking physical activity to breast cancer risk via insulin/insulin-like growth factor signaling system, part 1: the effect of physical activity on the insulin/insulin-like growth factor signaling system
.
Cancer Epidemiol Biomarkers Prev
2022
;
31
:
2106
15
.
16.
Drummond
AE
,
Swain
CTV
,
Milne
RL
,
English
DR
,
Brown
KA
,
Skinner
TL
, et al
.
Linking physical activity to breast cancer risk via the insulin/insulin-like growth factor signaling system, part 2: the effect of insulin/insulin-like growth factor signaling on breast cancer risk
.
Cancer Epidemiol Biomarkers Prev
2022
;
31
:
2116
25
.
17.
Orsini
N
.
Weighted mixed-effects dose–response models for tables of correlated contrasts
.
The Stata Journal
2021
;
21
:
320
47
.
18.
Morgan
RL
,
Thayer
KA
,
Santesso
N
,
Holloway
AC
,
Blain
R
,
Eftim
SE
, et al
.
A risk of bias instrument for non-randomized studies of exposures: a users' guide to its application in the context of grade
.
Environ Int
2019
;
122
:
168
84
.
19.
Guyatt
G
,
Oxman
AD
,
Akl
EA
,
Kunz
R
,
Vist
G
,
Brozek
J
, et al
.
Grade guidelines: 1. Introduction-grade evidence profiles and summary of findings tables
.
J Clin Epidemiol
2011
;
64
:
383
94
.
20.
Agnoli
C
,
Grioni
S
,
Pala
V
,
Allione
A
,
Matullo
G
,
Gaetano
CD
, et al
.
Biomarkers of inflammation and breast cancer risk: a case–control study nested in the EPIC-Varese cohort
.
Sci Rep
2017
;
7
:
12708
.
21.
Allin
KH
,
Bojesen
SE
,
Nordestgaard
BG
.
Inflammatory biomarkers and risk of cancer in 84,000 individuals from the general population
.
Int J Cancer
2016
;
139
:
1493
500
.
22.
Basu
S
,
Harris
H
,
Larsson
A
,
Vasson
MP
,
Wolk
A
.
Is there any role for serum cathepsin S and CRP levels on prognostic information in breast cancer? The Swedish Mammography Cohort
.
Antioxid Redox Signal
2015
;
23
:
1298
302
.
23.
Basu
S
,
Harris
H
,
Wolk
A
,
Rossary
A
,
Caldefie-Chezet
F
,
Vasson
MP
, et al
.
Inflammatory F2-isoprostane, prostaglandin F2α, pentraxin 3 levels, and breast cancer risk: The Swedish Mammography Cohort
.
Prostaglandins Leukot Essent Fatty Acids
2016
;
113
:
28
32
.
24.
Busch
EL
,
Whitsel
EA
,
Kroenke
CH
,
Yang
YC
.
Social relationships, inflammation markers, and breast cancer incidence in the Women's Health Initiative
.
Breast
2018
;
39
:
63
9
.
25.
Cui
Y
,
Shu
XO
,
Gao
YT
,
Cai
Q
,
Ji
BT
,
Li
HL
, et al
.
Urinary prostaglandin E2 metabolite and breast cancer risk
.
Cancer Epidemiol Biomarkers Prev
2014
;
23
:
2866
73
.
26.
Cust
AE
,
Stocks
T
,
Lukanova
A
,
Lundin
E
,
Hallmans
G
,
Kaaks
R
, et al
.
The influence of overweight and insulin resistance on breast cancer risk and tumor stage at diagnosis: a prospective study
.
Breast Cancer Res Treat
2009
;
113
:
567
76
.
27.
Dias
JA
,
Fredrikson
GN
,
Ericson
U
,
Gullberg
B
,
Hedblad
B
,
Engstrom
G
, et al
.
Low-grade inflammation, oxidative stress and risk of invasive postmenopausal breast cancer: a nested case–control study from the Malmö Diet and Cancer Cohort
.
PLoS One
2016
;
11
:
e0158959
.
28.
Dossus
L
,
Jimenez-Corona
A
,
Romieu
I
,
Boutron-Ruault
MC
,
Boutten
A
,
Dupre
T
, et al
.
C-reactive protein and postmenopausal breast cancer risk: results from the E3N Cohort Study
.
Cancer Causes Control
2014
;
25
:
533
9
.
29.
Frydenberg
H
,
Thune
I
,
Lofterod
T
,
Mortensen
ES
,
Eggen
AE
,
Risberg
T
, et al
.
Pre-diagnostic high-sensitive C-reactive protein and breast cancer risk, recurrence, and survival
.
Breast Cancer Res Treat
2016
;
155
:
345
54
.
30.
Gaudet
MM
,
Patel
AV
,
Teras
LR
,
Sun
J
,
Campbell
PT
,
Stevens
VL
, et al
.
Obesity-related markers and breast cancer in CPS-II Nutrition Cohort
.
Int J Mol Epidemiol Genet
2013
;
4
:
156
66
.
31.
Gaudet
MM
,
Falk
RT
,
Gierach
GL
,
Lacey
JV
Jr.
,
Graubard
BI
,
Dorgan
JF
, et al
.
Do adipokines underlie the association between known risk factors and breast cancer among a cohort of United States women?
Cancer Epidemiol
2010
;
34
:
580
6
.
32.
Gross
AL
,
Newschaffer
CJ
,
Hoffman-Bolton
J
,
Rifai
N
,
Visvanathan
K
.
Adipocytokines, inflammation, and breast cancer risk in postmenopausal women: a prospective study
.
Cancer Epidemiol Biomarkers Prev
2013
;
22
:
1319
24
.
33.
Gunter
MJ
,
Wang
T
,
Cushman
M
,
Xue
X
,
Wassertheil-Smoller
S
,
Strickler
HD
, et al
.
Circulating adipokines and inflammatory markers and postmenopausal breast cancer risk
.
J Natl Cancer Inst
2015
;
107
:
djv169
.
34.
Harris
HR
,
Tworoger
SS
,
Hankinson
SE
,
Rosner
BA
,
Michels
KB
.
Plasma leptin levels and risk of breast cancer in premenopausal women
.
Cancer Prev Res
2011
;
4
:
1449
56
.
35.
Heikkila
K
,
Harris
R
,
Lowe
G
,
Rumley
A
,
Yarnell
J
,
Gallacher
J
, et al
.
Associations of circulating C-reactive protein and interleukin 6 with cancer risk: findings from two prospective cohorts and a meta-analysis
.
Cancer Causes Control
2009
;
20
:
15
26
.
36.
Kim
S
,
Campbell
J
,
Yoo
W
,
Taylor
JA
,
Sandler
DP
.
Systemic levels of estrogens and PGE2 synthesis in relation to postmenopausal breast cancer risk
.
Cancer Epidemiol Biomarkers Prev
2017
;
26
:
383
8
.
37.
Kim
S
,
Taylor
JA
,
Milne
GL
,
Sandler
DP
.
Association between urinary prostaglandin E2 metabolite and breast cancer risk: a prospective, case–cohort study of postmenopausal women
.
Cancer Prev Res
2013
;
6
:
511
8
.
38.
Krajcik
RA
,
Massardo
S
,
Orentreich
N
.
No association between serum levels of tumor necrosis factor-alpha (TNF-alpha) or the soluble receptors sTNFR1 and sTNFR2 and breast cancer risk
.
Cancer Epidemiol Biomarkers Prev
2003
;
12
:
945
6
.
39.
Nelson
SH
,
Brasky
TM
,
Patterson
RE
,
Laughlin
GA
,
Kritz-Silverstein
D
,
Edwards
BJ
, et al
.
The association of the C-reactive protein inflammatory biomarker with breast cancer incidence and mortality in the Women's Health Initiative
.
Cancer Epidemiol Biomarkers Prev
2017
;
26
:
1100
6
.
40.
Ollberding
NJ
,
Kim
Y
,
Shvetsov
YB
,
Wilkens
LR
,
Franke
AA
,
Cooney
RV
, et al
.
Prediagnostic leptin, adiponectin, C-reactive protein, and the risk of postmenopausal breast cancer
.
Cancer Prev Res
2013
;
6
:
188
95
.
41.
Price
TR
,
Friedenreich
CM
,
Robson
PJ
,
Li
H
,
Brenner
DR
.
High-sensitivity C-reactive protein, hemoglobin A1c and breast cancer risk: a nested case–control study from Alberta's Tomorrow Project cohort
.
Cancer Causes Control
2020
;
31
:
1057
68
.
42.
Prizment
AE
,
Folsom
AR
,
Dreyfus
J
,
Anderson
KE
,
Visvanathan
K
,
Joshu
CE
, et al
.
Plasma C-reactive protein, genetic risk score, and risk of common cancers in the Atherosclerosis Risk in Communities study
.
Cancer Causes Control
2013
;
24
:
2077
87
.
43.
Shen
J
,
Hernandez
D
,
Ye
Y
,
Wu
X
,
Chow
WH
,
Zhao
H
.
Metabolic hormones and breast cancer risk among Mexican American women in the Mano a Mano Cohort study
.
Sci Rep
2019
;
9
:
9989
.
44.
Siemes
C
,
Visser
LE
,
Coebergh
JW
,
Splinter
TA
,
Witteman
JC
,
Uitterlinden
AG
, et al
.
C-reactive protein levels, variation in the C-reactive protein gene, and cancer risk: the Rotterdam Study
.
J Clin Oncol
2006
;
24
:
5216
22
.
45.
Stattin
P
,
Soderberg
S
,
Biessy
C
,
Lenner
P
,
Hallmans
G
,
Kaaks
R
, et al
.
Plasma leptin and breast cancer risk: a prospective study in northern Sweden
.
Breast Cancer Res Treat
2004
;
86
:
191
6
.
46.
Tobias
DK
,
Akinkuolie
AO
,
Chandler
PD
,
Lawler
PR
,
Manson
JE
,
Buring
JE
, et al
.
Markers of inflammation and incident breast cancer risk in the Women's Health Study
.
Am J Epidemiol
2018
;
187
:
705
16
.
47.
Touvier
M
,
Fezeu
L
,
Ahluwalia
N
,
Julia
C
,
Charnaux
N
,
Sutton
A
, et al
.
Association between prediagnostic biomarkers of inflammation and endothelial function and cancer risk: a nested case–control study
.
Am J Epidemiol
2013
;
177
:
3
13
.
48.
Tworoger
SS
,
Eliassen
AH
,
Kelesidis
T
,
Colditz
GA
,
Willett
WC
,
Mantzoros
CS
, et al
.
Plasma adiponectin concentrations and risk of incident breast cancer
.
J Clin Endocrinol Metab
2007
;
92
:
1510
6
.
49.
Van Hemelrijck
M
,
Holmberg
L
,
Garmo
H
,
Hammar
N
,
Walldius
G
,
Binda
E
, et al
.
Association between levels of C-reactive protein and leukocytes and cancer: three repeated measurements in the Swedish Amoris Study
.
Cancer Epidemiol Biomarkers Prev
2011
;
20
:
428
37
.
50.
Wang
G
,
Li
N
,
Chang
S
,
Bassig
BA
,
Guo
L
,
Ren
J
, et al
.
A prospective follow-up study of the relationship between C-reactive protein and human cancer risk in the Chinese Kailuan Female Cohort
.
Cancer Epidemiol Biomarkers Prev
2015
;
24
:
459
65
.
51.
Wulaningsih
W
,
Holmberg
L
,
Garmo
H
,
Malmstrom
H
,
Lambe
M
,
Hammar
N
, et al
.
Prediagnostic serum inflammatory markers in relation to breast cancer risk, severity at diagnosis, and survival in breast cancer patients
.
Carcinogenesis
2015
;
36
:
1121
8
.
52.
Zhang
SM
,
Lin
J
,
Cook
NR
,
Lee
IM
,
Manson
JE
,
Buring
JE
, et al
.
C-reactive protein and risk of breast cancer
.
J Natl Cancer Inst
2007
;
99
:
890
4
.
53.
Li
S
,
Xu
Y
,
Zhang
Y
,
Nie
L
,
Ma
Z
,
Ma
L
, et al
.
Mendelian randomization analyses of genetically predicted circulating levels of cytokines with risk of breast cancer
.
NPJ Precis Oncol
2020
;
4
:
25
.
54.
Robinson
T
,
Martin
RM
,
Yarmolinsky
J
.
Mendelian randomization analysis of circulating adipokines and C-reactive protein on breast cancer risk
.
Int J Cancer
2020
;
147
:
1597
603
.
55.
Yuan
S
,
Carter
P
,
Bruzelius
M
,
Vithayathil
M
,
Kar
S
,
Mason
AM
, et al
.
Effects of tumor necrosis factor on cardiovascular disease and cancer: a two-sample Mendelian randomization study
.
EBioMedicine
2020
;
59
.
56.
Ederveen
J
.
A practical approach to biological assay validation
.
Hoofddorp: Progress
2010
;
106
.
57.
Lawlor
DA
,
Tilling
K
,
Davey Smith
G
.
Triangulation in etiological epidemiology
.
Int J Epidemiol
2016
;
45
:
1866
86
.
58.
World Cancer Research Fund, American Institute for Cancer Research
.
Diet, nutrition, physical activity, and breast cancer
.
2018
.
59.
Duffy
DM
,
Ko
C
,
Jo
M
,
Brannstrom
M
,
Curry
TE
.
Ovulation: parallels with inflammatory processes
.
Endocr Rev
2019
;
40
:
369
416
.
60.
Anderson
KN
,
Schwab
RB
,
Martinez
ME
.
Reproductive risk factors and breast cancer subtypes: a review of the literature
.
Breast Cancer Res Treat
2014
;
144
:
1
10
.
61.
Wang
L
,
Zhang
R
,
Yu
L
,
Xiao
J
,
Zhou
X
,
Li
X
, et al
.
Aspirin use and common cancer risk: a meta-analysis of cohort studies and randomized controlled trials
.
Front Oncol
2021
;
11
:
690219
.
62.
King
J
,
Mir
H
,
Singh
S
.
Association of cytokines and chemokines in pathogenesis of breast cancer
.
Prog Mol Biol Transl Sci
2017
;
151
:
113
36
.
63.
Rose
DP
,
Vona-Davis
L
.
Biochemical and molecular mechanisms for the association between obesity, chronic inflammation, and breast cancer
.
Biofactors
2014
;
40
:
1
12
.
64.
Sproston
NR
,
Ashworth
JJ
.
Role of C-reactive protein at sites of inflammation and infection
.
Front Immunol
2018
;
9
:
754
.
65.
Jarde
T
,
Perrier
S
,
Vasson
MP
,
Caldefie-Chezet
F
.
Molecular mechanisms of leptin and adiponectin in breast cancer
.
Eur J Cancer
2011
;
47
:
33
43
.
66.
Nigro
E
,
Scudiero
O
,
Monaco
ML
,
Palmieri
A
,
Mazzarella
G
,
Costagliola
C
, et al
.
New insight into adiponectin role in obesity and obesity-related diseases
.
Biomed Res Int
2014
;
2014
:
658913
.
67.
Cruceriu
D
,
Baldasici
O
,
Balacescu
O
,
Berindan-Neagoe
I
.
I. The dual role of tumor necrosis factor-alpha (TNFα) in breast cancer: molecular insights and therapeutic approaches
.
Cell Oncol
2020
;
43
:
1
18
.
This open access article is distributed under the Creative Commons Attribution 4.0 International (CC BY 4.0) license.

Supplementary data