نتایج جستجو برای: brca2 gene

تعداد نتایج: 1143259  

2017
Cathy Su Alexis H. Haskins Chisato Omata Yasushi Aizawa Takamitsu A. Kato

High consumption of dietary flavonoids might contribute to a reduction of cancer risks. Quercetin and its glycosides have PARP inhibitory effects and can induce selective cytotoxicity in BRCA2-deficient cells by synthetic lethality. We hypothesized that common flavonoids in diet naringenin, hesperetin and their glycosides have a similar structure to quercetin, which might have comparable PARP i...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Anand D Jeyasekharan Nabieh Ayoub Robert Mahen Jonas Ries Alessandro Esposito Eeson Rajendra Hiroyoshi Hattori Rajan P Kulkarni Ashok R Venkitaraman

How the biochemical reactions that lead to the repair of DNA damage are controlled by the diffusion and availability of protein reactants within the nucleoplasm is poorly understood. Here, we use gene targeting to replace Brca2 (a cancer suppressor protein essential for DNA repair) with a functional enhanced green fluorescent protein (EGFP)-tagged form, followed by fluorescence correlation spec...

2013
Ryan B. Jensen

DNA damage, malfunctions in DNA repair, and genomic instability are processes that intersect at the crossroads of carcinogenesis. Underscoring the importance of DNA repair in breast and ovarian tumorigenesis is the familial inherited cancer predisposition gene BRCA2. The role of BRCA2 in DNA double-strand break repair was first revealed based on its interaction with RAD51, a central player in h...

Journal: :Endocrine-related cancer 2016
Amélie Fradet-Turcotte Justine Sitz Damien Grapton Alexandre Orthwein

Maintaining genomic integrity is essential to preserve normal cellular physiology and to prevent the emergence of several human pathologies including cancer. The breast cancer susceptibility gene 2 (BRCA2, also known as the Fanconi anemia (FA) complementation group D1 (FANCD1)) is a potent tumor suppressor that has been extensively studied in DNA double-stranded break (DSB) repair by homologous...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Shirley M H Sy Michael S Y Huen Junjie Chen

Mutations in breast cancer susceptibility gene 1 and 2 (BRCA1 and BRCA2) predispose individuals to breast and ovarian cancer development. We previously reported an in vivo interaction between BRCA1 and BRCA2. However, the biological significance of their association is thus far undefined. Here, we report that PALB2, the partner and localizer of BRCA2, binds directly to BRCA1, and serves as the ...

2017
Safoora Deihimi Avital Lev Michael Slifker Elena Shagisultanova Qifang Xu Kyungsuk Jung Namrata Vijayvergia Eric A. Ross Joanne Xiu Jeffrey Swensen Zoran Gatalica Mark Andrake Roland L. Dunbrack Wafik S. El-Deiry

Deficient mismatch repair (MMR) and microsatellite instability (MSI) contribute to ~15% of colorectal cancer (CRCs). We hypothesized MSI leads to mutations in DNA repair proteins including BRCA2 and cancer drivers including EGFR. We analyzed mutations among a discovery cohort of 26 MSI-High (MSI-H) and 558 non-MSI-H CRCs profiled at Caris Life Sciences. Caris-profiled MSI-H CRCs had high mutati...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2013
Joshy George Kathryn Alsop Dariush Etemadmoghadam Heather Hondow Thomas Mikeska Alexander Dobrovic Anna deFazio Gordon K Smyth Douglas A Levine Gillian Mitchell David D Bowtell

PURPOSE High-grade serous carcinoma (HGSC) accounts for the majority of epithelial ovarian cancer deaths. Genomic and functional data suggest that approximately half of unselected HGSC have disruption of the BRCA pathway and defects in homologous recombination repair (HRR). Pathway disruption is regarded as imparting a BRCAness phenotype. We explored the molecular changes in HGSC arising in ass...

2010
Kristiina Tamboom Krista Kaasik Jelena Aršavskaja Mare Tekkel Aili Lilleorg Peeter Padrik Andres Metspalu Toomas Veidebaum

BACKGROUND The aim of this study was to identify BRCA1 and BRCA2 mutations in the Estonian population. We analyzed genetic data and questionnaire from 64 early-onset (< 45 y) breast cancer patients, 47 familial cases (patients with breast or ovarian cancer and a case of these cancers in the family), and 33 predictive cases (patients without breast or ovarian cancer, with a family history of suc...

Journal: :Cancer research 1996
T Katagiri Y Nakamura Y Miki

To investigate whether the BRCA2 gene plays a role in carcinogenesis of hepatocellular carcinomas or pancreatic cancers in view of frequent losses of heterozygosity on chromosome 13q12-13 in those tumors, we screened the entire coding region of this gene for mutations in 60 hepatocellular carcinomas and 36 pancreatic cancers. No alteration was found in any of the pancreatic cancers examined, bu...

Journal: :Journal of medical genetics 2005
B Leegte A H van der Hout A M Deffenbaugh M K Bakker I M Mulder A ten Berge E P Leenders J Wesseling J de Hullu N Hoogerbrugge M J L Ligtenberg A Ardern-Jones E Bancroft A Salmon J Barwell R Eeles J C Oosterwijk

B Leegte, A H van der Hout, A M Deffenbaugh, M K Bakker, I M Mulder, A ten Berge, E P Leenders, J Wesseling, J de Hullu, N Hoogerbrugge, M J L Ligtenberg, A Ardern-Jones, E Bancroft, A Salmon, J Barwell, R Eeles, J C Oosterwijk . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ....

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