Literature DB >> 17483957

Microsomal glutathione S-transferase gene polymorphisms and colorectal cancer risk in a Han Chinese population.

Hao Zhang1, Ling-Hong Liao, Shuk-Ming Liu, Kwok-Wai Lau, Albert Kai-Cheong Lai, Jin-Hui Zhang, Qi Wang, Xiao-Qian Chen, Wei Wei, Hua Liu, Jian-Hua Cai, Maria Li Lung, Susan S W Tai, Madeline Wu.   

Abstract

BACKGROUND AND AIMS: Glutathione S-transferases (GSTs) are phase II detoxification enzymes. Human GSTs have been classified into cytosolic, mitochondrial, and microsomal families. Several studies reported the association of colorectal cancer (CRC) risk with the genetic polymorphisms of cytosolic GSTs. The microsomal GSTs are structurally distinct but functionally similar to cytosolic GSTs; their association with CRC has not been reported. In this report, we summarized the result of a case-control study aimed at investigating the association of MGST1 gene locus polymorphisms with CRC risk among Han Chinese. PATIENT/
METHODS: Three hundred and seventy-two healthy controls and 238 sporadic CRC patients participated in this study. DNA resequencing was conducted for the 3.4 kb genomic DNA region containing the promoter, exons, exon-intron junctions, and the 5' and 3' untranslated regions.
RESULTS: We detected 13 single nucleotide polymorphisms (SNPs) including four novel SNPs not reported in database/literature. The gene shows a much higher nucleotide diversity than most human genes. The linkage and recombination analysis revealed 24 common haplotypes (13% > or = freq > or = 1%) and identified extensive intragenic recombination throughout the MGST1 locus (R = 81.8). Significant CRC association (P < or = 0.005) was not detected for each individual SNP. However, SNPs 102G>A and 16416G>A reached a marginal level of statistical significance with P values of 0.016 and 0.078, respectively. A combined genotype analysis detected a statistically significant CRC association for individuals carrying 102G>A/16416G>A (GG/GG) genotype (adjusted OR, 1.682; 95% confidence interval (CI), 1.177-2.404; P = 0.004). Consistent with the results of genotype analysis, the GG haplotype (102G>A/16416G>A) with two risk alleles was associated with a significantly higher CRC risk comparing with the haplotypes with one or no risk allele (adjusted OR 1.744; 95% CI 1.309-2.322; P = 0.0001).
CONCLUSION: The results suggest that MGST1 polymorphisms may contribute to CRC risk among Han Chinese.

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Year:  2007        PMID: 17483957     DOI: 10.1007/s00384-007-0308-9

Source DB:  PubMed          Journal:  Int J Colorectal Dis        ISSN: 0179-1958            Impact factor:   2.571


  37 in total

1.  Structural organization of the microsomal glutathione S-transferase gene (MGST1) on chromosome 12p13.1-13.2. Identification of the correct promoter region and demonstration of transcriptional regulation in response to oxidative stress.

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2.  Haplotype variation and linkage disequilibrium in 313 human genes.

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Journal:  Science       Date:  2001-07-12       Impact factor: 47.728

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Journal:  Carcinogenesis       Date:  2000-10       Impact factor: 4.944

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Journal:  J Hum Genet       Date:  2001       Impact factor: 3.172

8.  Relationship between the GSTM1 genetic polymorphism and susceptibility to bladder, breast and colon cancer.

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Journal:  Carcinogenesis       Date:  1993-09       Impact factor: 4.944

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10.  Low nucleotide diversity in man.

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Journal:  Genetics       Date:  1991-10       Impact factor: 4.562

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  9 in total

1.  GSTM1 and GSTT1 polymorphisms and colorectal cancer risk in Chinese population: a meta-analysis.

Authors:  Dan Wang; Li-Mei Zhang; Jun-Xia Zhai; Dian-Wu Liu
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Authors:  Yi-Chen Dai; Xiao-San Zhu; Qing-Zhen Nan; Zhang-Xin Chen; Jun-Pei Xie; Yu-Ka Fu; Yuan-Yuan Lin; Qing-Na Lian; Qiao-Fang Sang; Xiao-Juan Zhan
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Journal:  World J Gastroenterol       Date:  2013-06-21       Impact factor: 5.742

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Journal:  Gut       Date:  2016-08-02       Impact factor: 23.059

6.  MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.

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Journal:  Cancer Med       Date:  2019-10-21       Impact factor: 4.452

7.  Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk.

Authors:  Ganna Chornokur; Hui-Yi Lin; Jonathan P Tyrer; Kate Lawrenson; Joe Dennis; Ernest K Amankwah; Xiaotao Qu; Ya-Yu Tsai; Heather S L Jim; Zhihua Chen; Ann Y Chen; Jennifer Permuth-Wey; Katja K H Aben; Hoda Anton-Culver; Natalia Antonenkova; Fiona Bruinsma; Elisa V Bandera; Yukie T Bean; Matthias W Beckmann; Maria Bisogna; Line Bjorge; Natalia Bogdanova; Louise A Brinton; Angela Brooks-Wilson; Clareann H Bunker; Ralf Butzow; Ian G Campbell; Karen Carty; Jenny Chang-Claude; Linda S Cook; Daniel W Cramer; Julie M Cunningham; Cezary Cybulski; Agnieszka Dansonka-Mieszkowska; Andreas du Bois; Evelyn Despierre; Ed Dicks; Jennifer A Doherty; Thilo Dörk; Matthias Dürst; Douglas F Easton; Diana M Eccles; Robert P Edwards; Arif B Ekici; Peter A Fasching; Brooke L Fridley; Yu-Tang Gao; Aleksandra Gentry-Maharaj; Graham G Giles; Rosalind Glasspool; Marc T Goodman; Jacek Gronwald; Patricia Harrington; Philipp Harter; Alexander Hein; Florian Heitz; Michelle A T Hildebrandt; Peter Hillemanns; Claus K Hogdall; Estrid Hogdall; Satoyo Hosono; Anna Jakubowska; Allan Jensen; Bu-Tian Ji; Beth Y Karlan; Linda E Kelemen; Mellissa Kellar; Lambertus A Kiemeney; Camilla Krakstad; Susanne K Kjaer; Jolanta Kupryjanczyk; Diether Lambrechts; Sandrina Lambrechts; Nhu D Le; Alice W Lee; Shashi Lele; Arto Leminen; Jenny Lester; Douglas A Levine; Dong Liang; Boon Kiong Lim; Jolanta Lissowska; Karen Lu; Jan Lubinski; Lene Lundvall; Leon F A G Massuger; Keitaro Matsuo; Valerie McGuire; John R McLaughlin; Iain McNeish; Usha Menon; Roger L Milne; Francesmary Modugno; Kirsten B Moysich; Roberta B Ness; Heli Nevanlinna; Ursula Eilber; Kunle Odunsi; Sara H Olson; Irene Orlow; Sandra Orsulic; Rachel Palmieri Weber; James Paul; Celeste L Pearce; Tanja Pejovic; Liisa M Pelttari; Malcolm C Pike; Elizabeth M Poole; Harvey A Risch; Barry Rosen; Mary Anne Rossing; Joseph H Rothstein; Anja Rudolph; Ingo B Runnebaum; Iwona K Rzepecka; Helga B Salvesen; Eva Schernhammer; Ira Schwaab; Xiao-Ou Shu; Yurii B Shvetsov; Nadeem Siddiqui; Weiva Sieh; Honglin Song; Melissa C Southey; Beata Spiewankiewicz; Lara Sucheston; Soo-Hwang Teo; Kathryn L Terry; Pamela J Thompson; Lotte Thomsen; Ingvild L Tangen; Shelley S Tworoger; Anne M van Altena; Robert A Vierkant; Ignace Vergote; Christine S Walsh; Shan Wang-Gohrke; Nicolas Wentzensen; Alice S Whittemore; Kristine G Wicklund; Lynne R Wilkens; Anna H Wu; Xifeng Wu; Yin-Ling Woo; Hannah Yang; Wei Zheng; Argyrios Ziogas; Hanis N Hasmad; Andrew Berchuck; Edwin S Iversen; Joellen M Schildkraut; Susan J Ramus; Ellen L Goode; Alvaro N A Monteiro; Simon A Gayther; Steven A Narod; Paul D P Pharoah; Thomas A Sellers; Catherine M Phelan
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8.  Japanese genome-wide association study identifies a significant colorectal cancer susceptibility locus at chromosome 10p14.

Authors:  Yusuke Takahashi; Keishi Sugimachi; Ken Yamamoto; Atsushi Niida; Teppei Shimamura; Tetsuya Sato; Masahiko Watanabe; Junichi Tanaka; Shinei Kudo; Kenichi Sugihara; Kazuo Hase; Masato Kusunoki; Kazutaka Yamada; Yasuhiro Shimada; Yoshihiro Moriya; Yutaka Suzuki; Satoru Miyano; Masaki Mori; Koshi Mimori
Journal:  Cancer Sci       Date:  2017-09-26       Impact factor: 6.716

9.  RNA-Seq Analysis Identified XLOC_009190 as Potential Therapeutic Target for Lung Adenocarcinoma.

Authors:  Jing Wang; Ning Wang; Wei-Dong Zhao; Li-Xian Zhao; Yong-Guang Jing; Li-Jie Yang; Jie He; Jun Li
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  9 in total

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