Literature DB >> 10944853

Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability.

H Orimo1, E Nakajima, M Yamamoto, M Ikejima, M Emi, T Shimada.   

Abstract

The association between three single nucleotide polymorphisms (SNPs) in the hMSH3 gene and sporadic colon cancer with microsatellite instability (MSI) was analyzed. Of the three SNPs observed in this population, SNPs at residues 235 and 693 were novel, while that at residue 3133 was previously described. The SNPs at residues 235 and 3133 caused amino acid substitutions, V79I and T1045A, respectively. We analyzed the allele frequencies of the three SNPs in samples from 19 patients with sporadic colon cancer with MSI and 90 healthy controls. We found that the V79 allele frequency was significantly higher in the tumor samples than in controls. In addition, the frequency of the G693 allele showed a higher trend in the tumor samples than in controls. These results indicated that some SNPs in the hMSH3 gene were associated with colon cancer with MSI.

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Year:  2000        PMID: 10944853     DOI: 10.1007/s100380070031

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  9 in total

1.  The MutSβ complex is a modulator of p53-driven tumorigenesis through its functions in both DNA double-strand break repair and mismatch repair.

Authors:  J M M van Oers; Y Edwards; R Chahwan; W Zhang; C Smith; X Pechuan; S Schaetzlein; B Jin; Y Wang; A Bergman; M D Scharff; W Edelmann
Journal:  Oncogene       Date:  2013-09-09       Impact factor: 9.867

2.  Aberrant protein expression and frequent allelic loss of MSH3 in colorectal cancer with low-level microsatellite instability.

Authors:  Jens Plaschke; Mark Preußler; Andreas Ziegler; Hans K Schackert
Journal:  Int J Colorectal Dis       Date:  2012-01-10       Impact factor: 2.571

3.  Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.

Authors:  Ronja Adam; Isabel Spier; Bixiao Zhao; Michael Kloth; Jonathan Marquez; Inga Hinrichsen; Jutta Kirfel; Aylar Tafazzoli; Sukanya Horpaopan; Siegfried Uhlhaas; Dietlinde Stienen; Nicolaus Friedrichs; Janine Altmüller; Andreas Laner; Stefanie Holzapfel; Sophia Peters; Katrin Kayser; Holger Thiele; Elke Holinski-Feder; Giancarlo Marra; Glen Kristiansen; Markus M Nöthen; Reinhard Büttner; Gabriela Möslein; Regina C Betz; Angela Brieger; Richard P Lifton; Stefan Aretz
Journal:  Am J Hum Genet       Date:  2016-07-28       Impact factor: 11.025

4.  Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.

Authors:  Monika Morak; Sarah Käsbauer; Martina Kerscher; Andreas Laner; Anke M Nissen; Anna Benet-Pagès; Hans K Schackert; Gisela Keller; Trisari Massdorf; Elke Holinski-Feder
Journal:  Fam Cancer       Date:  2017-10       Impact factor: 2.375

5.  MSH3 rs26279 polymorphism increases cancer risk: a meta-analysis.

Authors:  Hui-Kai Miao; Li-Ping Chen; Dong-Ping Cai; Wei-Ju Kong; Li Xiao; Jie Lin
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01

6.  Mismatch repair gene MSH3 polymorphism is associated with the risk of sporadic prostate cancer.

Authors:  Hiroshi Hirata; Yuji Hinoda; Ken Kawamoto; Nobuyuki Kikuno; Yutaka Suehiro; Naoko Okayama; Yuichiro Tanaka; Rajvir Dahiya
Journal:  J Urol       Date:  2008-03-20       Impact factor: 7.450

7.  Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation and homozygous truncating mutations.

Authors:  Anthony G Doran; Kim Wong; Jonathan Flint; David J Adams; Kent W Hunter; Thomas M Keane
Journal:  Genome Biol       Date:  2016-08-01       Impact factor: 13.583

8.  Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome.

Authors:  Raffaella Liccardo; Matilde Lambiase; Antonio Nolano; Marina De Rosa; Paola Izzo; Francesca Duraturo
Journal:  Int J Mol Med       Date:  2022-04-27       Impact factor: 5.314

Review 9.  DNA Mismatch Repair Gene Variants in Sporadic Solid Cancers.

Authors:  Fabian Caja; Ludmila Vodickova; Jan Kral; Veronika Vymetalkova; Alessio Naccarati; Pavel Vodicka
Journal:  Int J Mol Sci       Date:  2020-08-03       Impact factor: 5.923

  9 in total

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