نتایج جستجو برای: brca2

تعداد نتایج: 4162  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2008
Amber J Willems Sarah-Jane Dawson Hema Samaratunga Alessandro De Luca Yoland C Antill John L Hopper Heather J Thorne

PURPOSE Prostate cancer risk is increased for men carrying a pathogenic germline mutation in BRCA2, and perhaps BRCA1. Our primary aim was to test for loss of heterozygosity (LOH) at the locus of the mutation in prostate cancers from men who a carry pathogenic germline mutation in BRCA1 or BRCA2, and to assess clinical and pathologic features of these tumors. EXPERIMENTAL DESIGN From 1,243 kC...

Journal: :International journal of oncology 2007
Loredana Moro Arnaldo A Arbini Ersilia Marra Margherita Greco

BRCA2 is central to an utterly diverse biological behavior elicited after integrin-mediated normal and prostate cancer cell adhesion to basement membrane (BM) and extracellular matrix (ECM) proteins. Unlike normal cells, adhesive stimuli in cancer cells activate PI 3-kinase/AKT signaling resulting in BRCA2 degradation and unchecked cancer cell proliferation and metastasis. However, the precise ...

2017
Ming Cui Xian-Shu Gao Xiaobin Gu Wei Guo Xiaoying Li Mingwei Ma Shangbin Qin Xin Qi Mu Xie Chuan Peng Yun Bai

The aim of this study was to focus on clinicopathological characteristics and prognosis in men with prostate cancer (PCa) harboring a breast cancer 2 (BRCA2) gene mutation and to offer convincing evidence to consider BRCA2 mutation as a marker of poor prognosis in the molecular classification of PCa. We searched relevant articles from PubMed, Embase, Web of Science, and the Cochrane Library dat...

2008
Martha Klovstad Uri Abdu Trudi Schüpbach

Heterozygous mutations in the tumor suppressor BRCA2 confer a high risk of breast and other cancers in humans. BRCA2 maintains genome stability in part through the regulation of Rad51-dependent homologous recombination. Much about its precise function in the DNA damage responses is, however, not yet known. We have made null mutations in the Drosophila homolog of BRCA2 and measured the levels of...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2013
P M L H Vencken W Reitsma M Kriege M J E Mourits G H de Bock J A de Hullu A M van Altena K N Gaarenstroom H F A Vasen M A Adank M K Schmidt M van Beurden R P Zweemer F Rijcken B F M Slangen C W Burger C Seynaeve

BACKGROUND Recent studies suggested an improved overall survival (OS) for BRCA2- versus BRCA1-associated epithelial ovarian cancer (EOC), whereas the impact of chemotherapy is not yet clear. In a nationwide cohort, we examined the results of primary treatment, progression-free survival (PFS), treatment-free interval (TFI), and OS of BRCA1 versus BRCA2 EOC patients. METHODS Two hundred and for...

Journal: :Anticancer research 2005
L Le Corre C Vissac-Sabatier N Chalabi Y J Bignon A Daver A Chassevent D J Bernard-Gallon

The human DNA mismatch repair gene hMSH2 is involved in the development of sporadic and hereditary nonpolyposis colorectal cancer. An increased risk of colorectal cancer has also been suggested in BRCA1 and BRCA2 mutation carriers. To address the relationship between the expression level of these genes and colorectal tumorigenesis, we studied BRCA1, BRCA2 and hMSH2 mRNA expression by real-time ...

Journal: :Cancer research 1999
S S Yuan S Y Lee G Chen M Song G E Tomlinson E Y Lee

Mutations in BRCA1 and BRCA2 account for the majority of familial breast cancers. Cells with mutated BRCA1 or BRCA2 are hypersensitive to ionizing radiation (IR) and exhibit defective DNA repair. Both BRCA1 and BRCA2 have been reported to bind Rad51, a protein essential for homologous recombination and the recombinational repair of DNA double-strand breaks. In normal cells, a redistribution of ...

2015
Jun-hyeon Jeong Areum Jo Pilgu Park Hyunsook Lee Hae-Ock Lee

Germline mutations in the breast cancer type 2 susceptibility gene (BRCA2) are linked to familial breast cancer and the progressive bone marrow failure syndrome Fanconi anaemia. Established Brca2 mouse knockout models show embryonic lethality, but those with a truncating mutation at the C-terminus survive to birth and develop thymic lymphoma at an early age. To overcome early lethality and inve...

Journal: :American journal of human genetics 2008
Antonis C Antoniou Amanda B Spurdle Olga M Sinilnikova Sue Healey Karen A Pooley Rita K Schmutzler Beatrix Versmold Christoph Engel Alfons Meindl Norbert Arnold Wera Hofmann Christian Sutter Dieter Niederacher Helmut Deissler Trinidad Caldes Kati Kämpjärvi Heli Nevanlinna Jacques Simard Jonathan Beesley Xiaoqing Chen Susan L Neuhausen Timothy R Rebbeck Theresa Wagner Henry T Lynch Claudine Isaacs Jeffrey Weitzel Patricia A Ganz Mary B Daly Gail Tomlinson Olufunmilayo I Olopade Joanne L Blum Fergus J Couch Paolo Peterlongo Siranoush Manoukian Monica Barile Paolo Radice Csilla I Szabo Lutecia H Mateus Pereira Mark H Greene Gad Rennert Flavio Lejbkowicz Ofra Barnett-Griness Irene L Andrulis Hilmi Ozcelik Anne-Marie Gerdes Maria A Caligo Yael Laitman Bella Kaufman Roni Milgrom Eitan Friedman Susan M Domchek Katherine L Nathanson Ana Osorio Gemma Llort Roger L Milne Javier Benítez Ute Hamann Frans B L Hogervorst Peggy Manders Marjolijn J L Ligtenberg Ans M W van den Ouweland Susan Peock Margaret Cook Radka Platte D Gareth Evans Rosalind Eeles Gabriella Pichert Carol Chu Diana Eccles Rosemarie Davidson Fiona Douglas Andrew K Godwin Laure Barjhoux Sylvie Mazoyer Hagay Sobol Violaine Bourdon François Eisinger Agnès Chompret Corinne Capoulade Brigitte Bressac-de Paillerets Gilbert M Lenoir Marion Gauthier-Villars Claude Houdayer Dominique Stoppa-Lyonnet Georgia Chenevix-Trench Douglas F Easton

Germline mutations in BRCA1 and BRCA2 confer high risks of breast cancer. However, evidence suggests that these risks are modified by other genetic or environmental factors that cluster in families. A recent genome-wide association study has shown that common alleles at single nucleotide polymorphisms (SNPs) in FGFR2 (rs2981582), TNRC9 (rs3803662), and MAP3K1 (rs889312) are associated with incr...

Journal: :Cancer research 2008
Daniel J Farrugia Mukesh K Agarwal Vernon S Pankratz Amie M Deffenbaugh Dmitry Pruss Cynthia Frye Linda Wadum Kiley Johnson Jennifer Mentlick Sean V Tavtigian David E Goldgar Fergus J Couch

The assessment of the influence of many rare BRCA2 missense mutations on cancer risk has proved difficult. A multifactorial likelihood model that predicts the odds of cancer causality for missense variants is effective, but is limited by the availability of family data. As an alternative, we developed functional assays that measure the influence of missense mutations on the ability of BRCA2 to ...

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