نتایج جستجو برای: xrcc3 gene

تعداد نتایج: 1141511  

Journal: :Asian Pacific journal of cancer prevention : APJCP 2014
Saniya Nissar Aga Syed Sameer Tufail A Lone Nissar A Chowdri Roohi Rasool

XRCC (X-ray cross-complementing group) genes contribute to important DNA repair mechanisms that play roles in the repair of single strand breaks (SSBs) induced by a variety of external and internal factors, including ionizing radiation, alkylating agents and reactive oxygen species. These repair genes have a pivotal role in maintaining genomic stability through different pathways of base excisi...

2017
Mohammad Reza Sobhan Mohammad Forat Yazdi Mahta Mazaheri Masoud Zare Shehneh Hossein Neamatzadeh

Objective: Although there are a few studies investigating the relation between X-Ray Repair Cross Complementing 3 (XRCC3) gene rs861539 polymorphism and osteosarcoma (OSA), the results are inconsistent. Therefore, we performed this systematic review and meta-analysis to clarify the associations between XRCC3 rs861539 polymorphism and OSA risk. Methods: We have retrieved published literature fro...

2014
GAOFENG XU MAODE WANG WANFU XIE XIAOBIN BAI

The DNA repair gene, X-ray repair cross-complementing group 3 (XRCC3) Thr241Met polymorphism may be associated with a susceptibility to glioma. The present study aimed to investigate the association between the XRCC3 Thr241Met polymorphism and the potential susceptibility to gliomas. A hospital-based case-control study was conducted, which included a total of 886 patients with glioma and 886 he...

Journal: :Genetics and molecular research : GMR 2012
A C Custódio L O Almeida G R Pinto M J Santos J R W Almeida C A Clara J A Rey C Casartelli

The gene XRCC3 (X-ray cross complementing group 3) has the task of repairing damage that occurs when there is recombination between homologous chromosomes. Repair of recombination between homologous chromosomes plays an important role in maintaining genome integrity, although it is known that double-strand breaks are the main inducers of chromosomal aberrations. Changes in the XRCC3 protei...

Journal: :Genetics and molecular research : GMR 2010
R Attar C Cacina S Sozen E Attar B Agachan

Several polymorphisms in the DNA repair gene are thought to have significant effects on cancer risk. We investigated the association of polymorphisms in the DNA repair genes XRCC1 Arg399Gln, XRCC3 Thr241Met, XPD Lys751Gln, XPG Asp1104His, APE1 Asp148Glu, and HOGG1 Ser326Cys with endometriosis risk. Genotypes were determined by PCR-RFLP assays in 52 patients with endometriosis and 101 age-matche...

Journal: :Journal of the National Cancer Institute 2006
Christine B Ambrosone Peter G Shields Jo L Freudenheim Chi-Chen Hong

BACKGROUND The Breast Cancer Association Consortium (BCAC) is an international collaboration that was established to provide large sample sizes for examining genetic associations. We conducted combined analyses on all single-nucleotide polymorphisms (SNPs) whose associations with breast cancer have been investigated by at least three participating groups. METHODS Data from up to 12 studies we...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2016
Li Yan Qinghuai Li Xiaoyu Li Hong Ji Linlei Zhang

BACKGROUND/AIMS DNA HRR pathway and BER pathway play vital roles in differentiated thyroid cancer (DTC) development, thus we supposed that polymorphisms of XRCC1, XRCC2, XRCC3 DNA repair genes are associated with thyroid cancer risk and progression. METHODS We searched the NCBI database for relevant literatures to determine eight SNPs to be included in our study (XRCC1: rs25487, rs25489, rs17...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Claire Seedhouse Rowena Faulkner Nadia Ashraf Emma Das-Gupta Nigel Russell

PURPOSE Double-strand break repair via homologous recombination is essential in maintaining genetic integrity. RAD51 and XRCC3 are involved in the repair of DNA by this pathway, and polymorphisms have been identified in both the RAD51 (RAD51-G135C) and XRCC3 (XRCC3-Thr241Met) genes. The object of this study was to examine whether these polymorphisms may modulate susceptibility to the developmen...

2015
Jingjing Cheng Weiran Liu Xianliang Zeng Bin Zhang Yihang Guo Minghan Qiu Chao Jiang Huanhuan Wang Zhiqiang Wu Maobin Meng Hongqing Zhuang Lujun Zhao Jihui Hao Qingqing Cai Dan Xie Qingsong Pang Ping Wang Zhiyong Yuan Dong Qian

Radiotherapy is widely applied for treatment of esophageal squamous cell carcinoma (ESCC). The Rad51-related protein XRCC3 plays roles in the recombinational repair of DNA double-strand breaks to maintain chromosome stability and repair DNA damage. The present study aimed to investigate the effect of XRCC3 on the radiotherapy response of ESCC and the underlying mechanisms of the roles of XRCC3 ...

Journal: :Medical science monitor : international medical journal of experimental and clinical research 2015
Wenying Lu Guiqi Wu Bo Zhang

BACKGROUND The X-ray cross-complementing group 3 (XRCC3) gene encodes a protein that plays an important role in homologous recombination repair (HRR) of DNA double-strand break (DSB). Increasing attention has been drawn to the association of XRCC3 T241M polymorphism with various types of human cancers. In this study, a meta-analysis was performed to investigate whether there is an association b...

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