نتایج جستجو برای: ercc5

تعداد نتایج: 216  

Journal: :International journal of clinical and experimental pathology 2015
Nari Na Eer Dun Lidong Ren Guoxin Li

We conducted a case-control study to evaluate the association between ERCC5 polymorphism and breast cancer risk. 325 breast cancer patients and 325 controls were recruited in our study between January 2011 and March 2014. ERCC5 rs1047768, rs2094258, rs2296147, rs751402 and rs873601 polymorphisms were genotyped, using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) ...

2012
Mei-Ling Zhu Mengyun Wang Zhi-Gang Cao Jing He Ting-Yan Shi Kai-Qin Xia Li-Xin Qiu Qing-Yi Wei

BACKGROUND Excision repair cross complementing group 5 (ERCC5 or XPG) plays an important role in regulating DNA excision repair, removal of bulky lesions caused by environmental chemicals or UV light. Mutations in this gene cause a rare autosomal recessive syndrome, and its functional single nucleotide polymorphisms (SNPs) may alter DNA repair capacity phenotype and cancer risk. However, a seri...

2018
Jingwei Liu Hao Li Liping Sun Xue Feng Zhenning Wang Yuan Yuan Chengzhong Xing

Background Nucleotide excision repair (NER) plays a critical role in maintaining genome integrity. This study aimed to investigate the expression of NER genes and their associations with colorectal cancer (CRC) development. Method Expressions of NER genes in CRC and normal tissues were analysed by ONCOMINE. The Cancer Genome Atlas (TCGA) data were downloaded to explore relationship of NER exp...

2017
Meizhen Xu Yina Liu Dan Li Xuelin Wang Shuang Liang Gaochuan Zhang Xiaoqin Yang

It is suspected that ERCC5 rs1047768 and rs17655 polymorphisms influence the response to platinum-based chemotherapy. This meta-analysis was performed to summarize the scattered evidence regarding the association between these two polymorphisms and sensitivity to platinum-based treatment. Thirteen studies were included after a comprehensive literature search. The pooled odds ratios and 95% conf...

ERCC5 plays crucial role in excision repair DNA damage induced by UV in NER pathway. Single neuleotide polymorphism in ERCC5 were responsible for different cancers.Therefore, current study evaluated the relationship between ERCC5 (rs1047768 T>C) polymorphism and the risk of breast cancer in Pakistani population. The rs1047768 polymorphism was screened among 175 female...

ERCC5 plays crucial role in excision repair DNA damage induced by UV in NER pathway. Single neuleotide polymorphism in ERCC5 were responsible for different cancers.Therefore, current study evaluated the relationship between ERCC5 (rs1047768 T>C) polymorphism and the risk of breast cancer in Pakistani population. The rs1047768 polymorphism was screened among 175 female...

Journal: :Farmakogenetika i farmakogenomika 2023

Цель . Изучение связи полиморфных маркеров генов репарации ДНК ERCC2 (rs13181), ERCC5 (rs17655), транспортного белка ABCB1 (rs1045642, rs2032582) с клиническим ответом и степенью патоморфологической регрессии (ПР) опухоли у беременных женщин онкологическими заболеваниями после ХТ препаратами платины.

Journal: :Carcinogenesis 2000
L Cheng M R Spitz W K Hong Q Wei

Epidemiological studies have indicated that reduced DNA repair capacity and increased DNA adduct levels are associated with increased risk of lung cancer. Nucleotide excision repair (NER) is the major pathway in humans for repairing DNA adducts induced by smoking-related carcinogens, such as benzo[a]pyrene diol epoxide. We hypothesized that genetically determined baseline expression level of ge...

2018
Jiyoun Yeo Diego A. Morales Tian Chen Erin L. Crawford Xiaolu Zhang Thomas M. Blomquist Albert M. Levin Pierre P. Massion Douglas A. Arenberg David E. Midthun Peter J. Mazzone Steven D. Nathan Ronald J. Wainz Patrick Nana-Sinkam Paige F. S. Willey Taylor J. Arend Karanbir Padda Shuhao Qiu Alexei Federov Dawn-Alita R. Hernandez Jeffrey R. Hammersley Youngsook Yoon Fadi Safi Sadik A. Khuder James C. Willey

BACKGROUND There is a need for more powerful methods to identify low-effect SNPs that contribute to hereditary COPD pathogenesis. We hypothesized that SNPs contributing to COPD risk through cis-regulatory effects are enriched in genes comprised by bronchial epithelial cell (BEC) expression patterns associated with COPD. METHODS To test this hypothesis, normal BEC specimens were obtained by br...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2013
Ke-Qin Luo Shi-Qing Mu Zhong-Xue Wu Yi-Ni Shi Ji-Cai Peng

Polymorphisms in DNA repair genes have been shown to influence DNA repair processes and to modify cancer susceptibility. Here we conducted a case-control study to assess the role of potential SNPs of DNA repair genes on the risk of glioma and meningioma. We included 297 cases and 458 cancer-free controls. Genotyping of XRCC1 Gln399Arg, XRCC1 Arg194Trp, XRCC2 Arg188His, XRCC3 Thr241Met, XRCC4 Al...

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