POTENTIAL CONSEQUENCES OF THE BRCA1 MUTATION CARRIER STATE ON ESTROGEN RESPONSIVE ORGANS
| Autor: | Yen, Hai-Yun, Gabet, Yankel, Liu, Ying, Martin, Anthony, Wu, Nancy L, Pike, Malcolm C, Frenkel, Baruch, Maxson, Robert, Dubeau, Louis |
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| Jazyk: | angličtina |
| Rok vydání: | 2012 |
| Předmět: |
endocrine system
Genotype Genes BRCA1 Osteoclasts Estrous Cycle Familial cancer predisposition Article Hormonal carcinogenesis Mouse model Endometrium Mice Aromatase Ovarian cancer Animals Genetic Predisposition to Disease Femur Cell Proliferation Mice Knockout Granulosa Cells Estradiol BRCA1 Protein Stem Cells Cell Differentiation Estrogens BRCA1 Mice Inbred C57BL Animals Newborn Female Estrus Synchronization |
| Zdroj: | Laboratory investigation; a journal of technical methods and pathology |
| ISSN: | 1530-0307 0023-6837 |
| Popis: | Incessant menstrual cycle activity, uninterrupted by either pregnancy or oral contraceptive use, is the most important risk factor for sporadic ovarian cancer. Menstrual cycle progression is partly controlled by steroid hormones such as estrogens and others that are secreted by the ovarian granulosa cells. We showed earlier that mice carrying a homozygous granulosa cell-specific knockout of Brca1, the homolog of BRCA1 that is associated with familial ovarian cancer predisposition in humans, develop benign epithelial tumors in their reproductive tract. These tumors are driven, at least in part, by a prolongation of the proestrus phase of the estrus cycle (equivalent to the follicular phase of the menstrual cycle) in Brca1 mutant mice, resulting in prolonged unopposed estrogen stimulation. Mutant mice synchronized in proestrus also showed increased circulating estradiol levels, but the possibility that this change also has a role in tumor predisposition was not investigated. We sought to determine whether these changes in hormonal stimulation result in measurable changes in tissues targeted by estrogen outside the ovary. Here we show that mice carrying a Brca1 mutation in their ovarian granulosa cells show increased endometrial proliferation during proestrus, implying that the effects of Brca1 inactivation on estrogen stimulation have short-term consequences, at least on this target organ. We further show that mutant mice develop increased femoral trabecular thickness and femoral length, which are well-known consequences of chronic estrogen stimulation. Estrogen biosynthesis by granulosa cells was increased not only in mice carrying a homozygous Brca1 mutation, but also in heterozygous mutants mimicking the mutational status in granulosa cells of human BRCA1 mutation carriers. The results suggest that human germline BRCA1 mutations, although associated with increased cancer risk, may also have beneficial consequences, such as increased bone strength, that may have contributed to the maintenance of mutated BRCA1 alleles in the human gene pool. |
| Databáze: | OpenAIRE |
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