نتایج جستجو برای: xrcc1

تعداد نتایج: 1139  

2015
Xin-Xin Chi You-Yu Liu Su-Ning Shi Zhuang Cong Yu-Qing Liang Hui-Jun Zhang

OBJECTIVE This meta-analysis aimed to determine the relationships between XRCC1 Arg399Gln (rs25487 G>A) and XPD Lys751Gln (rs1052559 A>C) polymorphisms and susceptibility to age-related cataract. METHODS Medline (1966-2013), the Cochrane Library Database (Issue 12, 2013), EMBASE (1980-2013), CINAHL (1982-2013), Web of Science (1945-2013) and the Chinese Biomedical Database (CBM; 1982-2013) we...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2008
Feng-Yu Chiang Che-Wei Wu Pi-Jung Hsiao Wen-Rei Kuo Ka-Wo Lee Jen-Chih Lin Yi-Chu Liao Suh-Hang Hank Juo

PURPOSE DNA BER pathway is related with carcinogenesis. We hypothesized that functional polymorphisms of three BER genes, XRCC1, apurinic/apyrimidinic endonuclease (APE1), and ADPRT, confer risks for DTC and its progression. EXPERIMENTAL DESIGN Five common nonsynonymous single nucleotide polymorphisms (Arg194Trp, Arg280His, and Arg399Gln for XRCC1; Asp148Glu for APE1; and Val762Ala for ADPRT)...

Journal: :Carcinogenesis 2006
Chunying Li Zhensheng Liu Li-E Wang Sara S Strom Jeffrey E Lee Jeffrey E Gershenwald Merrick I Ross Paul F Mansfield Janice N Cormier Victor G Prieto Madeleine Duvic Elizabeth A Grimm Qingyi Wei

Sunlight causes various kinds of DNA damage, including oxidative lesions that are removed effectively by the base excision repair (BER) pathway, in which ADPRT, XRCC1 and APE1 play a key role. However, genetic variation in these genes may alter their functions. We hypothesized that ADPRT, XRCC1 and APE1 polymorphisms are associated with risk of cutaneous melanoma (CM). In a hospital-based case-...

2016
Wen-Qi Ma Xi-Qiong Han Xin Wang Ying Wang Yi Zhu Nai-Feng Liu

Genetic variations that influence DNA repair efficiency may contribute to coronary artery disease (CAD) susceptibility. Previous studies have investigated whether there was evidence of an association between polymorphisms at the X-ray repair cross complementing 1 (XRCC1) gene and susceptibility to CAD, but findings have been inconclusive. We identified eligible studies through a comprehensive l...

2015
Mi Yuanyuan You Xiaoming Zhu Lijie Feng Ninghan

OBJECTIVE The polymorphism in codon 399 of the X-ray repair cross-complementing group 1 (XRCC1) gene may subtly alter structure of DNA repair enzymes and modulate the repair capacity. Impaired DNA repair can lead to the development of cancers such as prostate cancer (PCA). Although the association between the XRCC1 codon 399 polymorphism and PCA risk has been extensively reported, the results h...

2014
Aziz Zaanan Cécile Dalban Jean-François Emile Hélène Blons Jean-François Fléjou Claire Goumard Melek Istanbullu Claire Calmel Khalid Alhazmi Pierre Validire Christophe Louvet Aimery de Gramont Pierre Laurent-Puig Julien Taïeb Françoise Praz

BACKGROUND While single nucleotide polymorphisms (SNP) in genes involved in DNA repair or drug metabolism have been shown to influence survival of metastatic colon cancer patients treated with FOLFOX, data on adjuvant setting are scarce. METHODS This study evaluated the correlation between disease-free survival (DFS) of 210 unselected stage III colon cancer patients receiving FOLFOX chemother...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2012
Yi Gan Xiao-Rong Li Dao-Jin Chen Jun-Hui Wu

We conducted this study to detect associations between XRCC1 Arg399Gln and XPD Lys751Gln genotypes and survival of colorectal cancer patients treated with 5-FU/oxalipatin chemotherapy. We included 289 Chinese patients with advanced colorectal cancer, who had received 5-FU/oxalipatin chemotherapy as first-line treatment from January 2005 to January 2007. All patients were followed up till Nov. 2...

2013
Liang Zhang Yan Wang Zhiqun Qiu Jiaohua Luo Ziyuan Zhou Weiqun Shu

OBJECTIVES Previous reports indicated that XRCC1 Arg280His polymorphism might be a possible risk factor for several cancers. Published studies on the association of XRCC1 Arg280His polymorphisms with glioma risk have yielded controversial results. The present study aimed to derive a more precise estimation of the relationship. METHODOLOGY Meta-analyses assessing the association of XRCC1 Arg28...

Journal: :Carcinogenesis 2010
Qi Wang Fang Ji Yuan Sun Yu-Lan Qiu Wei Wang Fen Wu Wen-Bin Miao Yongliang Li Paul W Brandt-Rauf Zhao-Lin Xia

In this study, a group of 313 workers occupationally exposed to vinyl chloride monomer (VCM) and 141 normal unexposed referents were examined for chromosomal damage using the cytokinesis-blocked micronucleus (CBMN) assay in peripheral lymphocytes. We explored the relationship between genetic polymorphisms of XRCC1 (Arg194Trp, Arg280His and Arg399Gln), MGMT(Leu84Phe) and hOGG1 (Ser326Cys) and su...

2015
Haipeng Zhu Tao Jiu Dong Wang

OBJECTIVE We conducted a case-control study to examine the role of XRCC1 codons 194 (Arg>Trp), 280 (Arg>His) and 399 (Arg>Gln) polymorphisms in the risk of prostate cancer. METHODS This study included 572 consecutive primary prostate cancer patients and 572 controls between January 2011 and January 2014. The polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was per...

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