نتایج جستجو برای: mlh1

تعداد نتایج: 1941  

Journal: :Cancer research 2001
R A Hardman C A Afshari J C Barrett

MLH1 is an integral part of the mismatch repair complex, and the loss of this protein is associated with the acquisition of a mutator phenotype, microsatellite instability, and a predisposition to cancer. Deficiencies in the mismatch repair complex, including the loss of MLH1, result in elevated resistance to specific inducers of DNA damage, yet the mechanisms involved in this DNA-damage resist...

Journal: :Journal of medical genetics 1996
N J Froggatt C Brassett D J Koch D G Evans S V Hodgson B A Ponder E R Maher

Germline mutations in four human mismatch repair genes (MSH2, MLH1, PMS1, and PMS2) have been reported to cause hereditary non-polyposis colon cancer syndrome (HNPCC). The identification of germline mutations in HNPCC kindreds allows precise diagnosis and accurate predictive testing. To investigate further the genetic epidemiology of HNPCC and the nature and frequency of germline mutations in t...

2016
Takashi Takeda Kouji Banno Megumi Yanokura Masataka Adachi Moito Iijima Haruko Kunitomi Kanako Nakamura Miho Iida Yuya Nogami Kiyoko Umene Kenta Masuda Yusuke Kobayashi Wataru Yamagami Akira Hirasawa Eiichiro Tominaga Nobuyuki Susumu Daisuke Aoki

Germline mutation of DNA mismatch repair (MMR) genes is a cause of Lynch syndrome. Methylation of MutL homolog 1 (MLH1) and MutS homolog 2 (MSH2) has been detected in peripheral blood cells of patients with colorectal cancer. This methylation is referred to as epimutation. Methylation of these genes has not been studied in an unselected series of endometrial cancer cases. Therefore, we examined...

2015
PAVEL VODICKA FABIAN CAJA VERONIKA VYMETALKOVA PAVEL PROCHAZKA LUDMILA VODICKOVA LUCIE SCHWARZOVA JANA SLYSKOVA RAJIV KUMAR MICHAELA SCHNEIDEROVA

Mutations in the mutL homolog 1 (MLH1) gene are frequent in patients with hereditary non-polyposis colorectal cancer (CRC). The MLH1 gene was screened for mutations in patients with sporadic CRC. The nucleotide sequences for all 19 exons of MLH1 were analyzed by high resolution melting and sequenced in a group of 104 sporadic CRC patients, and the results were verified in a replication group of...

2015
Chao-Hua Chiu Hsiang-Ling Ho Howard Doong Yi-Chen Yeh Mei-Yu Chen Teh-Ying Chou Chun-Ming Tsai

A significant fraction of patients with lung adenocarcinomas harboring activating epidermal growth factor receptor (EGFR) mutations do not experience clinical benefits from EGFR tyrosine kinase inhibitor (TKI) therapy. Using next-generation sequencing, we screened 739 mutation hotspots in 46 cancer-related genes in EGFR L858R-mutant lung adenocarcinomas from 29 patients who received EGFR-TKI th...

2014
Yanqun Liu Min Hoe Chew Xue Wei Goh Soo Yong Tan Carol Tien Tau Loi Yuen Ming Tan Hai Yang Law Poh Koon Koh Choong Leong Tang

BACKGROUND Germline defects of mismatch repair (MMR) genes underlie Lynch Syndrome (LS). We aimed to gain comprehensive genetic and epigenetic profiles of LS families in Singapore, which will facilitate efficient molecular diagnosis of LS in Singapore and the region. METHODS Fifty nine unrelated families were studied. Mutations in exons, splice-site junctions and promoters of five MMR genes w...

Journal: :Blood 2011
Davide Rossi Silvia Rasi Alice Di Rocco Alberto Fabbri Francesco Forconi Annunziata Gloghini Alessio Bruscaggin Silvia Franceschetti Marco Fangazio Lorenzo De Paoli Riccardo Bruna Daniela Capello Annalisa Chiappella Chiara Lobetti Bodoni Manuela Giachelia Maria Chiara Tisi Enrico M Pogliani Francesco Lauria Marco Ladetto Stefan Hohaus Maurizio Martelli Umberto Vitolo Antonino Carbone Robin Foà Gianluca Gaidano

Several drugs used for diffuse large B-cell lymphoma (DLBCL) treatment rely on DNA damage for tumor cell killing. We verified the prognostic impact of the host DNA repair genotype in 2 independent cohorts of DLBCL treated with R-CHOP21 (training cohort, 163 cases; validation cohort, 145 cases). Among 35 single nucleotide polymorphisms analyzed in the training series, MLH1 rs1799977 was the sole...

2011
Constantinos Giaginis Christina Michailidi Vasileios Stolakis Paraskevi Alexandrou Gerasimos Tsourouflis Jerzy Klijanienko Ioanna Delladetsima Stamatios Theocharis

BACKGROUND DNA repair is a major defense mechanism, which contributes to the maintenance of genetic sequence, and minimizes cell death, mutation rates, replication errors, DNA damage persistence and genomic instability. Alterations in the expression levels of proteins participating in DNA repair mechanisms have been associated with several aspects of cancer biology. The present study aimed to e...

Journal: :DNA repair 2004
Laura A Bannister Barbara Criscuolo Waldman Alan S Waldman

We assayed error-prone double-strand break (DSB) repair in wild-type and isogenic Mlh1-null mouse embryonic fibroblasts containing a stably integrated DSB repair substrate. The substrate contained a thymidine kinase (tk) gene fused to a neomycin-resistance (neo) gene; the tk-neo fusion gene was disrupted in the tk portion by a 22bp oligonucleotide containing the 18 bp recognition site for endon...

2015
ZHIWEI CHANG WEIJIE ZHANG ZHIJUN CHANG MIN SONG YANRU QIN FUBAO CHANG HAIYUN GUO QINGLI WEI

The aim of the present study was to determine the changes to the expression levels of fragile histidine triad (FHIT), breast cancer type 2 susceptibility protein (BRCA2), MutL homolog 1 (MLH1) and tumour protein 53 (p53) exhibited by families with a history of oesophageal cancer in a region that has a high incidence of oesophageal cancer, and to determine the association of these changes with t...

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