Your browser doesn't support javascript.
loading
Frequent loss of BRCA1 mRNA and protein expression in sporadic ovarian cancers.
Russell, P A; Pharoah, P D; De Foy, K; Ramus, S J; Symmonds, I; Wilson, A; Scott, I; Ponder, B A; Gayther, S A.
Affiliation
  • Russell PA; CRC Department of Oncology, Strangeways Research Laboratory, Cambridge, UK. paul.russell@srl.cam.ac.uk
Int J Cancer ; 87(3): 317-21, 2000 Aug 01.
Article in En | MEDLINE | ID: mdl-10897034
Germline mutations in the BRCA1 gene cause inherited susceptibility to breast and ovarian cancers. However, somatic mutations of BRCA1 are rare in sporadic breast and ovarian tumours. To establish whether BRCA1 is altered during the development of sporadic ovarian cancer by mechanisms other than somatic mutation, we have analysed 57 sporadic epithelial ovarian tumours for BRCA1 protein and RNA expression. Reduced or absent protein expression was observed in 90% of tumours. Decreased protein expression was significantly associated with a reduction in the levels of RNA expression. Somatic mutations of BRCA1 and LOH at the BRCA1 locus were detected in 3.5% and 44% of informative tumours, respectively; there was no significant correlation between the levels of protein and RNA expression and the DNA mutation and/or LOH status. Together, these data suggest that expression of BRCA1 is down-regulated at the level of transcription during the development of sporadic ovarian cancers.
Subject(s)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms / RNA, Messenger / RNA, Neoplasm / Gene Deletion / BRCA1 Protein / Genes, BRCA1 / Loss of Heterozygosity / Mutation / Neoplasm Proteins Limits: Female / Humans Language: En Journal: Int J Cancer Year: 2000 Document type: Article Country of publication: United States
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms / RNA, Messenger / RNA, Neoplasm / Gene Deletion / BRCA1 Protein / Genes, BRCA1 / Loss of Heterozygosity / Mutation / Neoplasm Proteins Limits: Female / Humans Language: En Journal: Int J Cancer Year: 2000 Document type: Article Country of publication: United States