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The FANC-BRCA pathway is disrupted in a subset of ovarian tumor lines.

Women's Health Weekly

| July 03, 2003 | COPYRIGHT 2003 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2003 JUL 3 - (NewsRx.com & NewsRx.net) -- The FANC-BRCA pathway is disrupted in a subset of ovarian tumor lines.

"Ovarian tumor cells are often genomically unstable and hypersensitive to cisplatin. To understand the molecular basis for this phenotype, we examined the integrity of the Fanconi anemia-BRCA (FANC-BRCA) pathway in those cells," researchers in England report.

"This pathway regulates cisplatin sensitivity and is governed by the coordinate activity of six genes associated with Fanconi anemia (FANCA, FANCC, FANCD2, FANCE, FANCF and FANCG) as well as BRCA1 and BRCA2 (FANCD1). Here we show that," wrote T. Taniguchi and colleagues, Guys Kings & St. Thomas School of Medicine, Dana Farber Cancer Institute.

"Mono-ubiquitination of FANCD2, a measure of the function of this pathway, and cisplatin resistance were restored by functional complementation with FANCF, a gene that is upstream in this pathway," the researchers stated.

The researchers concluded: "FANCF inactivation in ...

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Source: HighBeam Research, The FANC-BRCA pathway is disrupted in a subset of ovarian tumor lines.

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