Small-cell lung carcinoma (SCLC) is a neuroendocrine subtype of lung cancer. Although SCLC patients often initially respond to therapy, tumors nearly always recur, resulting in a 5-year survival rate of less than 10%. A mouse model has been developed based on the fact that the RB and p53 tumor suppressor genes are mutated in more than 90% of human SCLCs. Emerging evidence in patients and mouse models suggests that p130, a gene related to RB, may act as a tumor suppressor in SCLC cells. To test this idea, we used conditional mutant mice to delete p130 in combination with Rb and p53 in adult lung epithelial cells. We found that loss of p130 resulted in increased proliferation and significant acceleration of SCLC development in this triple-knockout mouse model. The histopathologic features of the triple-mutant mouse tumors closely resembled that of human SCLC. Genome-wide expression profiling experiments further showed that Rb/p53/p130-mutant mouse tumors were similar to human SCLC. These findings indicate that p130 plays a key tumor suppressor role in SCLC. Rb/p53/p130-mutant mice provide a novel preclinical mouse model to identify novel therapeutic targets against SCLC. Cancer Res; 70(10); 3877–83. ©2010 AACR.

The prognosis for patients suffering from small-cell lung carcinoma (SCLC) has not improved in the past 25 years. Despite advances in chemotherapy and radiation therapy regimens, 5-year survival rates for SCLC remain only 5% to 10%. At the time of diagnosis, SCLC has often already metastasized, and patients almost always relapse following treatment (1).

Based on the observation that the RB and p53 tumor suppressor genes are both mutated in more than 90% of human SCLC, a mouse model for human SCLC has been generated. In this model, Cre-mediated deletion of Rb and p53 conditional alleles in the lungs of adult mice results in the development of tumors that share many characteristics with human SCLC, including their histopathology, the expression of neuroendocrine markers, and their ability to metastasize (2). This mouse model provides a system to identify genetic and epigenetic changes that may contribute to the development of SCLC, in addition to loss of Rb and p53 (2, 3). In particular, emerging evidence suggests that p130, a cell cycle inhibitor related to RB (4), may normally suppress SCLC development. The first report describing loss of p130 in a human cancer was in SCLC (5). In addition, low levels of the p130 protein have been associated with a higher histologic grade, increased proliferation, and a trend toward poorer patient survival (68). Recent evidence further indicates that p130 mRNA levels may be downregulated in lung cancer cells by members of the miR-17-92 microRNA cluster, which is often overexpressed in human SCLC and may play a role in the expansion of neuroendocrine cells (9, 10). The possibility that p130 is a bona fide tumor suppressor has gained further support in mice where loss of p130 cooperates with loss of Rb in retinoblastoma development (11) and in the development of small neuroendocrine lung lesions (12). Similarly, loss of E2F4, a major partner for p130, partially suppresses lung neuroendocrine hyperplasias in Rb-mutant mice (13). Loss of p130 also results in the acceleration of tumorigenesis in a mouse model for human lung adenocarcinoma (14). Interestingly, although p130 shares many characteristics with p107, the third member of the RB family, there is no evidence that p107 may be involved in the suppression of SCLC (5, 12). Here, we tested the tumor suppressor role of p130 in SCLC using a mouse genetics approach. We found that loss of p130 accelerates the development of SCLC in Rb/p53-mutant mice and that Rb/p53/p130-mutant mice provide an improved mouse model of SCLC.

Mice and adenoviral infections

Conditional mutant Rb and p53 mice were bred to mice with a conditional allele for p130 (refs. 2, 15; Supplementary Fig. S1 and Supplementary Methods). Adenoviral infections were done as described (14). Mice were maintained at the Stanford Research Animal Facility accredited by the Association for Assessment and Accreditation of Laboratory Animal Care.

DNA, RNA, and microarray analysis

Genomic DNA was prepared using lysis buffer containing Proteinase K (Sigma Aldrich). RNA was isolated from tumors or control lungs using TRIzol (Invitrogen). The Dynamo cDNA Synthesis Kit (New England Biolabs) was used to prepare cDNA from RNA. Real-time quantitative PCR was done on an ABI Prism 7900HT Sequence Detection System with the SYBR GreenER qPCR mix (Invitrogen). The Ct value of each sample was normalized using the values for the TATA binding protein gene (TBP). Primer sequences are listed in Supplementary Tables S1 and S2. Affymetrix 430-2.0 arrays were hybridized and analyzed at the Stanford Microarray facility as described (ref. 15; Supplementary Methods).

Immunoblot analysis and immunostaining

For immunoblot analysis (14), the antibodies used were p130 (BD Biosciences), p107 (Santa Cruz), synaptophysin (SYP; Neomarkers), karyopherin β1 (Santa Cruz), and α-tubulin (Sigma).

Paraffin sections were rehydrated in Trilogy reagent (Cell Marque). Sections were mounted in ProLong Gold Antifade reagent (Invitrogen) after immunostaining (14). The primary antibodies used were phospho-histone 3 Ser10 (PH3; Millipore), bromodeoxyuridine (BrdUrd) (Becton-Dickinson), Ki67 (BD Biosciences), MCM6 (Santa Cruz Biotechnology), proliferating cell nuclear antigen (PCNA; Santa Cruz Biotechnology), surfactant protein C (SP-C; Dr. Jeff Whitsett, University of Cincinnati, Cincinnati, OH), Clara cell secretory protein (CCSP; Santa Cruz Biotechnology), and SYP (Neomarkers). Alexa Fluor secondary antibodies (Invitrogen) were used for antibody detection. Quantification was done using the Bio-Quant image analysis software.

Statistics

Statistical significance was assayed by Student's t test with the Prism GraphPad software.

To test the possibility that p130 may act as a tumor suppressor gene in SCLC, we performed intranasal instillation of adenovirus expressing the Cre recombinase (Ad-Cre) in Rb/p53/p130 triple conditional mutant mice (Fig. 1A). After 6 months, primary lung tumors and liver metastases were detected at the surface of these organs; no other tumor types were identified in the mutant mice at this time point (Fig. 1B and data not shown; see below). PCR analysis on genomic DNA showed deletion of the three genes in the tumor cells but not in tail DNA in all cases examined (Fig. 1C). Quantitative reverse transcription-PCR (RT-PCR) analysis confirmed the decreased expression of these three genes in the triple-mutant tumors (Fig. 1D). Finally, immunoblot analysis showed depletion of the p130 protein in all the triple-mutant tumors analyzed (Supplementary Fig. S2). p107 levels increased similarly in double- and triple-mutant tumors compared with wild-type lungs (Fig. 1D; Supplementary Fig. S2), indicating that loss of p130 does not induce p107 expression in SCLC cells. Together, these experiments suggest that loss of p130 is not counter-selected during tumorigenesis, allowing us to test the role of p130 in SCLC development. Recent observations indicate that the combined loss of Rb and p130 is not sufficient for SCLC development in mice (16). The fact that we did not find tumors that were only p53/p130 mutant is also suggestive that loss of p130 does not alleviate the need for loss of Rb in SCLC, but this idea remains to be directly tested in p53/p130-mutant mice.

To determine the functional role of p130 in SCLC development, we compared tumorigenesis in the lungs of Rb/p53- and Rb/p53/p130-mutant mice. We found that 6 months after Ad-Cre infection, few tumors were present at the surface of the lungs of Rb/p53-mutant mice, as reported (2). In contrast, a number of tumors were visible in the lungs of Rb/p53/p130-mutant mice (Fig. 1B). Histologic examination confirmed that tumors were rarely found at this time point in Rb/p53-mutant lungs, whereas tumors of various sizes were present in Rb/p53/p130-mutant lungs (Fig. 2A). Even 3 months after Ad-Cre infection, numerous lesions were readily identified in sections of Rb/p53/p130-mutant lungs, whereas similar-sized lesions were observed 6 months after infection of Rb/p53-mutant mice (Fig. 2A).Tumor burden was measured in the lungs of Rb/p53/p130-mutant mice 6 months after Ad-Cre infection and was similar to that of Rb/p53-mutant mice 9 to 12 months after infection (Fig. 2B). Not only did the triple-mutant mice developed tumors more rapidly but they also developed significantly more tumors than the double-mutant animals (Fig. 2C). We found that very few double-mutant mice died before 28 weeks (data not shown), similar to what was described before (2). In contrast, one triple-mutant mouse died at 17 weeks, another at 19 weeks, and two at 26 weeks; in addition, all the Rb/p53/p130-mutant mice analyzed at the 6-month time point were moribund. Although we have not performed a complete survival analysis, these observations suggest that Rb/p53/p130-mutant mice may die faster than Rb/p53-mutant mice with the dose of Ad-Cre used in these studies. Thus, p130 is a potent suppressor of lung cancer initiated by loss of Rb and p53 functions in mice.

p130 is a known regulator of cell cycle progression (4), which led us to examine the proliferative status of double- and triple-mutant tumor cells in vivo. Immunostaining for Ki67, a marker of cycling cells, and PCNA and MCM6, two markers of S phase, showed that both double- and triple-mutant cells were actively proliferating (Supplementary Fig. S3). Quantitative analysis of the mitotic index of tumors using immunostaining for phospho-histone 3 (PH3) further indicated that triple-mutant tumors had more cells in G2-M than double-mutant tumors of similar sizes (Fig. 2D). These data suggest that one mechanism of tumor suppression by p130 in SCLC is to limit the proliferation of Rb/p53-mutant cells (see below), without excluding the possibility that p130 loss may accelerate SCLC development by other mechanisms. In particular, p130 loss could change the type of lung cancer developing in the mutant mice. Although histopathologic analysis showed that a few lesions had some characteristic of lung adenocarcinomas, adenocarcinomas with neuroendocrine features, large-cell neuroendocrine carcinomas, and large-cell carcinomas, all these were present in mice from both genotypes. Furthermore, the large majority of tumors developing in Rb/p53- and Rb/p53/p130-mutant mice had clear architectural, cytologic, and clinical features of human SCLC (Fig. 2A, Supplementary Fig. S4, and data not shown). Furthermore, although the number of mice analyzed thus far remains limited, another striking phenotype of the Rb/p53/p130-mutant model is a high incidence of metastasis to the liver, one of the primary organs to which SCLC is known to metastasize in patients. Three of five Rb/p53/p130 mice had several liver metastases 6 months after Ad-Cre infection, whereas no lesions were identified in Rb/p53 mice at the same time point and a lower incidence of liver metastasis was observed or previously reported at 9 months or later time points (Supplementary Fig. S4 and data not shown; ref. 2). In addition, Rb/p53p130 mice developed metastases to pulmonary lymph nodes and kidney, two common sites of metastasis of human SCLC (Supplementary Fig. S4).

We next examined the expression of lung cancer markers in Rb/p53/p130-mutant tumors. Immunostaining analysis showed that triple-mutant lesions expressed SYP, a synaptic vesicle protein used as a marker for human SCLC, but were largely negative for SP-C and CCSP, two markers of lung alveolar and bronchiolar epithelial cells, respectively, similar to Rb/p53-mutant tumors (Fig. 3A). Even 1 month after Ad-Cre infection, at a time when no lesions are visible in Rb/p53-mutant mice, small triple-mutant lesions were evident. Cells in these lesions were dividing, as assessed by BrdUrd incorporation, and expressed SYP (Fig. 3B). Moreover, quantitative RT-PCR showed that all Rb/p53/p130-mutant tumors examined expressed typical markers of human SCLC such as Cgrp, Syp, Ncam1, and Ascl1 (ref. 17; Fig. 3C). Immunoblot analysis further indicated that the triple-mutant tumor cells expressed the SYP protein (Fig. 3D). Cell lines derived from triple- and double-knockout mutant tumors grew in floating clusters, similar to human SCLC cells (18); the mouse tumor cells also retained the expression of SYP, but, as expected, Rb/p53/p130-mutant tumor cells did not express p130 (Supplementary Fig. S5).

To compare genome-wide expression profiles in Rb/p53- and Rb/p53/p130-mutant tumors, we performed a microarray analysis with double-mutant tumors 9 months after Ad-Cre infection and with triple-mutant tumors 6 months after Ad-Cre infection. Although this difference in time could affect tumor evolution in the two models, the histology and the size of double- and triple-mutant tumors at these time points are similar (Fig. 2A and B). Significant analysis of microarrays (SAM) showed that only 151 genes were differentially expressed between the two genotypes of a total of 14,712 genes, with a minimal 1.5-fold change of expression level and a false discovery rate of 10% or lower (Supplementary Fig. S6). This observation strongly indicates that tumors from the two genotypes are very similar at the level of global gene expression. Using DAVID bioinformatics tools, we found that a few of the differentially expressed genes were implicated in the control of cell cycle progression (Supplementary Fig. S6A). Quantitative RT-PCR analysis confirmed increased levels of the tyrosine kinase gene c-Yes and the DNA repair gene Rad54l in Rb/p53/p130-mutant tumors compared with Rb/p53-mutant tumors; in contrast, the expression of classic E2F targets such as genes coding for B-Myb, cyclin E, and PCNA was not significantly different (Supplementary Fig. S7). The functional role of the genes whose expression is significantly different in triple-knockout tumors and the mechanisms underlying the increased proliferation of triple-mutant cells versus double-mutant cells will be investigated in future experiments.

We next compared the data sets from the mouse models to data sets from human SCLC and non–small-cell lung cancer (NSCLC); because SCLC patients rarely undergo surgery, less than 50 genome-wide transcription profiling microarray data for primary human SCLC samples are currently publicly available (1921); the 13 data sets from double- and triple-mutant mouse tumors increase the number of primary tumors analyzed by more than 25%. A number of genes overexpressed in human SCLC were readily identified in the list of overexpressed genes in Rb/p53/p130- and Rb/p53-mutant tumors (Fig. 4A). Gene set enrichment analysis further showed that the genes overexpressed in human SCLC were significantly enriched in Rb/p53/p130-mutant tumors (Supplementary Fig. S8). Importantly, cross-specific clustering analysis showed that the two mouse models clustered with human SCLC rather than with normal lung or NSCLC (Fig. 4B). Taken together, these findings extend the similarity between the Rb/p53- and Rb/p53/p130-mutant lung tumors and human SCLC from the histopathologic level to global gene expression, further validating the Rb/p53/p130-mutant mouse model.

In conclusion, the ablation of p130 in the context of Rb and p53 loss accelerates tumor development while maintaining the overall histopathologic and molecular features of SCLC. Our data directly show that p130 serves a potent tumor suppression function in murine SCLC. Loss of p130 function results in increased proliferation, providing an explanation for why reduced p130 levels may be selected in human tumors. Compared with Rb/p53-mutant mice, Rb/p53/p130-mutant mice develop more tumors at a faster rate and will be instrumental in exploring the mechanisms of SCLC initiation, progression, and metastasis. Future studies will use different doses of virus to change tumor burden and explore the long-term survival and phenotypes of the triple-mutant mice. This novel mouse model for human SCLC will also serve to identify novel diagnostic markers and therapeutic targets against this deadly cancer.

No potential conflicts of interest were disclosed.

We thank Dr. J. Kissil for critical reading of the manuscript and Drs. J. Whitsett and A. Berns (Netherlands Cancer Institute, Amsterdam, The Netherlands) for the generous gift of SP-C antibodies and p53lox mice, respectively. We apologize to our colleagues whose important work is not cited because of space considerations.

Grant Support: The American Lung Association (J. Sage and K-S. Park), the Parker B. Francis Fellowship Program (K-S. Park), the California Tobacco-Related Disease Research Program (J.F. Conklin), the California Breast Cancer Research Program Dissertation Fellowship (D.L. Burkhart), the Damon Runyon Cancer Research Foundation (J. Sage), and the American Cancer Society (J. Sage).

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

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