Literature DB >> 19538867

[Association between Fas/Fas L genes promoter polymorphisms and pathogenic risk of cervical cancer].

Hua Li1, Hong-yan Guo, Tong Sun, Yi-feng Zhou, Dong-xin Lin, Wen-hua Zhang, Jie Qiao.   

Abstract

OBJECTIVE: To investigate the association between apoptosis genes Fas/Fas L promoter polymorphisms and the risk of the development of cervical cancer.
METHODS: Blood samples were collected from 314 cases with primary cervical cancer and 615 healthy controls. Genotypes of Fas/Fas L genes were determined by polymerase chain reaction-based restriction fragment length polymorphism. The associations with the risk of cervical cancer and impact of clinicopathological characteristics were estimated by logistic regression.
RESULTS: Fas L-844CC genotype was significantly associated with increased risk of cervical cancer compared with Fas L-844TC or -TT genotype (OR = 3.05; P < 0.01). However, there was no significant difference of Fas-670A/G or -1377G/A genotypes. Interaction of genetic polymorphism between Fas and Fas L was observed. Stratification analysis revealed that Fas-670G or -1377A allele was significantly higher in squamous carcinoma in situ (OR = 1.77 or 1.93; P < 0.05) while Fas L-844CC genotype had an increased risk of invasive squamous carcinoma compared with that of Fas L-844TT genotype (OR = 3.33; P < 0.01). No significant associations were observed between polymorphisms in Fas/Fas L and clinical FIGO stage, cell differentiation, size of tumors, serum squamous cell carcinoma antigen value at the diagnosis and so on.
CONCLUSION: The results of this study suggest that genetic polymorphisms of Fas and Fas L in apoptotic pathway are associated with the risk of development of cervical carcinoma.

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Year:  2009        PMID: 19538867

Source DB:  PubMed          Journal:  Zhonghua Zhong Liu Za Zhi        ISSN: 0253-3766


  12 in total

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Authors:  Yan Zhang; Shengchun Tong; Lihua Guan; Fei Na; Wei Zhao; Li Wei
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2.  Genetic association between CD95 rs2234767 polymorphism and cervical cancer risk: a meta analysis.

Authors:  Ping Liu; Zibai Wei; Xiaofeng He; Junyan Yu; Xiangyang Tian; Jianlan Chang
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3.  Significant association among the Fas -670 A/G (rs1800682) polymorphism and esophageal cancer, hepatocellular carcinoma, and prostate cancer susceptibility: a meta-analysis.

Authors:  Tao Liu; Li Zuo; Lin Li; Lei Yin; Kai Liang; Hongyuan Yu; Hui Ren; Wen Zhou; Hongwei Jing; Yang Liu; Chuize Kong
Journal:  Tumour Biol       Date:  2014-08-02

4.  Letter regarding Wang GQ et al. entitled "associations between Fas/FasL polymorphisms and susceptibility to cervical cancer: a meta-analysis".

Authors:  Ying Zeng; Jia Liu; Jinjin Yan; Hui Liu; Shuhua Xiong
Journal:  Tumour Biol       Date:  2014-07-04

5.  Association between CD95L polymorphism and cervical cancer risk: evidence from a meta-analysis.

Authors:  Jing Zhu; Lei Lu; Xiang Cheng; Rongkai Xie; Zhengqiong Chen; Youfei Li; Guilan Lin; Jianmei Liu; Ying Yang
Journal:  Tumour Biol       Date:  2014-03-12

6.  Promoter polymorphism of FASL confers protection against female-specific cancers and those of FAS impact the cancers divergently.

Authors:  Sateesh Reddy Nallapalle; Sarika Daripally; V T S Vidudala Prasad
Journal:  Tumour Biol       Date:  2014-12-04

Review 7.  Genetic susceptibility to cervical cancer: role of common polymorphisms in apoptosis-related genes.

Authors:  Shing Cheng Tan; Ravindran Ankathil
Journal:  Tumour Biol       Date:  2015-08-05

8.  FAS-670 gene polymorphism and cervical carcinogenesis risk: A meta-analysis.

Authors:  Qiaoying Huang; Jie Wang; Yanling Hu
Journal:  Biomed Rep       Date:  2013-08-20

9.  CD95 rs1800682A/G variant and tumor risk in Asians: evidence from a meta-analysis of 36 case-control studies containing 22,438 samples.

Authors:  Cheng Jin; Xiaomin Wu; Yuanlong Gu; Fenglai Yuan; Qinghai Ye; Feng Dai; Lijie Zhu; Yuanyuan Mi
Journal:  Med Sci Monit       Date:  2015-02-27

10.  Associations between Fas/FasL polymorphisms and susceptibility to cervical cancer: a meta-analysis.

Authors:  Guo-qing Wang; Lei Bao; Xi-xia Zhao; Jun Zhang; Ke-jun Nan
Journal:  Tumour Biol       Date:  2013-12-28
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