Proliferation and differentiation are important processes within the ovaries and testes. Uncontrolled proliferation results in cancer whereas failure to differentiate can result in infertility. Cell cycle regulators and TGF(3 superfamily signaling pathways play key roles in both processes. Cyclin D2 null mice have decreased granulosa cell proliferation and smaller testes whereas p27 null mice have increased Sertoli cell proliferation and defects in granulosa cell terminal differentiation. With the support of this grant, we have shown that the inhibins, a:p members of the TGFp superfamily, function in the gonads as tumor suppressors and that cyclin D2/inhibin a double mutants have slowed tumor development whereas p27/inhibin a double mutants die of gonadal tumors very rapidly. Both gonadotropins (FSH and LH) are also involved in the tumorigenesis process. Given the emerging relationship between cyclin D2, FSH, and the retinoblastoma (RB) tumor suppressor in granulosa cells and consistent with findings that the RB pathway is deregulated in most human cancers, our working model is that RB is central to the development of these ovarian and testicular cancers. Our overall hypothesis is that the inhibin/activin/BMP, RB/E2F, FSH, LH, and cell cycle pathways converge to regulate the G1 to S phase transition and that modulation of the activity (phosphorylation) state of RB by cell cycle regulators (e.g., cyclin D2/CDK4, cyclin E2(E1)/CDK2, and p27) and inhibin determines the proliferation and terminal differentiation of granulosa or Sertoli cells, ultimately affecting the predisposition of these cells to cancer.
The Specific Aims of the proposed studies are: 1) Define the physiologic roles of the retinoblastoma (RB) tumor suppressor in granulosa cell and Sertoli cell proliferation and differentiation;2) Determine if the RB protein is a genetic modifier of tumor development in the inhibin a knockout model;3) Establish the relative roles of luteinizing hormone (LH) and follicle stimulating hormone (FSH) in granulosa cell and Sertoli cell proliferation, differentiation, and tumor development;and 4) Characterize the alterations in cell cycle regulation, cell adhesion, and responsiveness to LH that occur early in the transformation of granulosa cells into cancer. Characterization of these mice will lead to important insights into the development of gonadal cancers in men and women and the roles of several proteins in reproductive physiology.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA060651-18
Application #
7769891
Study Section
Special Emphasis Panel (ZRG1-EMNR-H (03))
Program Officer
Yassin, Rihab R,
Project Start
1993-08-01
Project End
2012-02-28
Budget Start
2010-03-08
Budget End
2012-02-28
Support Year
18
Fiscal Year
2010
Total Cost
$266,562
Indirect Cost
Name
Baylor College of Medicine
Department
Pathology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Matzuk, Martin M; Burns, Kathleen H (2012) Genetics of mammalian reproduction: modeling the end of the germline. Annu Rev Physiol 74:503-28
Roy, Angshumoy; Matzuk, Martin M (2011) Reproductive tract function and dysfunction in women. Nat Rev Endocrinol 7:517-25
Hawkins, Shannon M; Buchold, Gregory M; Matzuk, Martin M (2011) Minireview: The roles of small RNA pathways in reproductive medicine. Mol Endocrinol 25:1257-79
Rajanahally, Saneal; Agno, Julio E; Nalam, Roopa L et al. (2010) Genetic evidence that SMAD2 is not required for gonadal tumor development in inhibin-deficient mice. Reprod Biol Endocrinol 8:69
Nagaraja, Ankur K; Creighton, Chad J; Yu, Zhifeng et al. (2010) A link between mir-100 and FRAP1/mTOR in clear cell ovarian cancer. Mol Endocrinol 24:447-63
Nalam, Roopa L; Andreu-Vieyra, Claudia; Matzuk, Martin M (2010) Absence of inhibin alpha and retinoblastoma protein leads to early sertoli cell dysfunction. PLoS One 5:e11797
Creighton, Chad J; Benham, Ashley L; Zhu, Huifeng et al. (2010) Discovery of novel microRNAs in female reproductive tract using next generation sequencing. PLoS One 5:e9637
Nagaraja, Ankur K; Middlebrook, Brooke S; Rajanahally, Saneal et al. (2010) Defective gonadotropin-dependent ovarian folliculogenesis and granulosa cell gene expression in inhibin-deficient mice. Endocrinology 151:4994-5006
Nalam, Roopa L; Matzuk, Martin M (2010) Local signalling environments and human male infertility: what we can learn from mouse models. Expert Rev Mol Med 12:e15
Hawkins, S M; Matzuk, M M (2010) Oocyte-somatic cell communication and microRNA function in the ovary. Ann Endocrinol (Paris) 71:144-8

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