The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancer

<p>Abstract</p> <p>Mutations within the BRCA1 tumor suppressor gene occur frequently in familial epithelial ovarian carcinomas but they are a rare event in the much more prevalent sporadic form of the disease. However, decreased BRCA1 expression occurs frequently in sporadic tumors...

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Main Authors: Mueller Christopher R, McCoy Marcia L, Roskelley Calvin D
Format: Article
Language:English
Published: BMC 2003-10-01
Series:Reproductive Biology and Endocrinology
Online Access:http://www.RBEj.com/content/1/1/72
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spelling doaj-14d0a12aa44743919e484008f44fb59e2020-11-24T21:19:08ZengBMCReproductive Biology and Endocrinology1477-78272003-10-01117210.1186/1477-7827-1-72The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancerMueller Christopher RMcCoy Marcia LRoskelley Calvin D<p>Abstract</p> <p>Mutations within the BRCA1 tumor suppressor gene occur frequently in familial epithelial ovarian carcinomas but they are a rare event in the much more prevalent sporadic form of the disease. However, decreased BRCA1 expression occurs frequently in sporadic tumors, and the magnitude of this decrease has been correlated with increased disease progression. The near absence of somatic mutations consequently suggests that there are alternative mechanisms that may contribute to the observed loss of BRCA1 in sporadic tumors. Indeed, both allelic loss at the BRCA1 locus and epigenetic hypermethylation of the BRCA1 promoter play an important role in BRCA1 down-regulation; yet these mechanisms alone or in combination do not always account for the reduced BRCA1 expression. Alternatively, misregulation of specific upstream factors that control BRCA1 transcription may be a crucial means by which BRCA1 is lost. Therefore, determining how regulators of BRCA1 expression may be co-opted during sporadic ovarian tumorigenesis will lead to a better understanding of ovarian cancer etiology and it may help foster the future development of novel therapeutic strategies aimed at halting ovarian tumor progression.</p> http://www.RBEj.com/content/1/1/72
collection DOAJ
language English
format Article
sources DOAJ
author Mueller Christopher R
McCoy Marcia L
Roskelley Calvin D
spellingShingle Mueller Christopher R
McCoy Marcia L
Roskelley Calvin D
The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancer
Reproductive Biology and Endocrinology
author_facet Mueller Christopher R
McCoy Marcia L
Roskelley Calvin D
author_sort Mueller Christopher R
title The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancer
title_short The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancer
title_full The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancer
title_fullStr The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancer
title_full_unstemmed The role of the breast cancer susceptibility gene 1 (BRCA1) in sporadic epithelial ovarian cancer
title_sort role of the breast cancer susceptibility gene 1 (brca1) in sporadic epithelial ovarian cancer
publisher BMC
series Reproductive Biology and Endocrinology
issn 1477-7827
publishDate 2003-10-01
description <p>Abstract</p> <p>Mutations within the BRCA1 tumor suppressor gene occur frequently in familial epithelial ovarian carcinomas but they are a rare event in the much more prevalent sporadic form of the disease. However, decreased BRCA1 expression occurs frequently in sporadic tumors, and the magnitude of this decrease has been correlated with increased disease progression. The near absence of somatic mutations consequently suggests that there are alternative mechanisms that may contribute to the observed loss of BRCA1 in sporadic tumors. Indeed, both allelic loss at the BRCA1 locus and epigenetic hypermethylation of the BRCA1 promoter play an important role in BRCA1 down-regulation; yet these mechanisms alone or in combination do not always account for the reduced BRCA1 expression. Alternatively, misregulation of specific upstream factors that control BRCA1 transcription may be a crucial means by which BRCA1 is lost. Therefore, determining how regulators of BRCA1 expression may be co-opted during sporadic ovarian tumorigenesis will lead to a better understanding of ovarian cancer etiology and it may help foster the future development of novel therapeutic strategies aimed at halting ovarian tumor progression.</p>
url http://www.RBEj.com/content/1/1/72
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