نتایج جستجو برای: brca mutation

تعداد نتایج: 292614  

Journal: :Cancer research 2006
Jennifer K Hockings Patricia A Thorne Michael Q Kemp Sherif S Morgan Ornella Selmin Donato F Romagnolo

In sporadic breast cancers, BRCA-1 expression is down-regulated in the absence of mutations in the BRCA-1 gene. This suggests that disruption of BRCA-1 expression may contribute to the onset of mammary tumors. Environmental contaminants found in industrial pollution, tobacco smoke, and cooked foods include benzo(a)pyrene [B(a)P] and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), which have been sh...

2017
Kai Xu Shouhua Yang Yingchao Zhao

There is no consensus on the syntheses concerning the impact of BRCA mutation on ovarian cancer survival. A systematic review and meta-analysis of observational studies was conducted that evaluated the impact of BRCA mutations on the survival outcomes of patients with ovarian cancer. The primary outcome measure was overall survival (OS) and secondary outcome was progression-free survival (PFS)....

2016
Andrea L Amico Rimas V Lukas Hedy L Kindler

Leptomeningeal carcinomatosis from pancreatic cancer is a rare finding thought to occur late in the natural history of the disease. Here we present two cases of leptomeningeal carcinomatosis from BRCA mutation-associated pancreatic cancer including one patient in whom it developed during treatment with a PARP-inhibitor. We review the literature and discuss the possibility that BRCA-associated p...

Journal: :Obstetrical & Gynecological Survey 2023

(Abstracted from J Clin Oncol 2022; doi: 10.1200/JCO.22.01549) Because of nonspecific symptoms at disease presentation and inadequate screening methods, ovarian cancer is often advanced the time diagnosis results in a 10-year survival 17% patients with epithelial cancer. The poly(ADP-ribose) polymerase (PARP) inhibitor olaparib new standard care newly diagnosed BRCA1 and/or BRCA2 (BRCA) mutation.

Journal: :Journal of clinical pathology 1999
R P Zweemer P A Shaw R M Verheijen A Ryan A Berchuck B A Ponder H Risch J R McLaughlin S A Narod F H Menko P Kenemans I J Jacobs

BACKGROUND Mutations in the BRCA1 or BRCA2 genes are responsible for up to 95% of hereditary ovarian cancer cases. Both genes function as tumour suppressor genes, and development of a cancer is thought to require an accumulation of somatic genetic events in addition to the inherited germline predisposition. It is unknown whether these somatic events in BRCA associated ovarian cancer are similar...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2008
N Hoogerbrugge Y J L Kamm P Bult K M Landsbergen E M H F Bongers H G Brunner H J Bonenkamp J A de Hullu M J L Ligtenberg C Boetes

PURPOSE To assess the false-positive rate of breast cancer surveillance by magnetic resonance imaging (MRI) in BRCA mutation carriers and the impact of an abnormal mammography or breast MRI on the patients' decision for prophylactic mastectomy. PATIENTS AND METHODS A total of 196 BRCA mutation carriers were included with a median follow-up of 2 years (range 1-9) with annual mammography and MR...

2015
Soley Bayraktar Hongming Qiu Diane Liu Yu Shen Angelica M Gutierrez-Barrera Banu K Arun Aysegul A Sahin

BACKGROUND Several studies have evaluated histologic features of non-neoplastic breast parenchyma in patients with BRCA1/2 mutations, but the results are conflicting. The limited data suggest a much higher prevalence of high-risk precursor lesions in BRCA carriers. Therefore, we designed this study to compare the clinicopathological characteristics of peritumoral benign breast tissue in patient...

2016
Po-Han Lin Wen-Hung Kuo Ai-Chu Huang Yen-Shen Lu Ching-Hung Lin Sung-Hsin Kuo Ming-Yang Wang Chun-Yu Liu Fiona Tsui-Fen Cheng Ming-Hsin Yeh Huei-Ying Li Yu-Hsuan Yang Yu-Hua Hsu Sheng-Chih Fan Long-Yuan Li Sung-Liang Yu King-Jen Chang Pei-Lung Chen Yen-Hsuan Ni Chiun-Sheng Huang

Since BRCA mutations are only responsible for 10-20% of cases of breast cancer in patients with early-onset or a family history and since next-generation sequencing technology allows the simultaneous sequencing of a large number of target genes, testing for multiple cancer-predisposing genes is now being considered, but its significance in clinical practice remains unclear. We then developed a ...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005
Jeffrey N Weitzel Mark Robson Barbara Pasini Siranoush Manoukian Dominique Stoppa-Lyonnet Henry T Lynch Jane McLennan William D Foulkes Teresa Wagner Nadine Tung Parviz Ghadirian Olufunmilayo Olopade Claudine Isaacs Charmaine Kim-Sing Pal Møller Susan L Neuhausen Kelly Metcalfe Ping Sun Steven A Narod

BACKGROUND Women with breast cancer and a BRCA mutation have a high risk of developing a contralateral breast cancer. It is generally believed that the two cancers represent independent events. However, the extent of concordance between the first and second tumors with respect to hormone receptor expression and other pathologic features is unknown. PURPOSE To determine the degree of concordan...

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