Literature DB >> 11918085

Is reduced expression of mismatch repair genes MLH1 and MSH2 in patients with sporadic colorectal cancer related to their prognosis?

Martin Kruschewski1, Aurelia Noske, Jörg Haier, Norbert Runkel, Yanis Anagnostopoulos, Heinz Johannes Buhr.   

Abstract

The majority of mutations in hereditary nonpolyposis colon carcinoma (HNPCC) patients affect the mismatch-repair genes (MMRG) MLHI and MSH2. In addition, mutations of these genes were found in about 15% of sporadic colorectal carcinomas which appear to be related to microsatellite instability (MSI). However, mutations in MMRG were not found in all MSI-positive carcinomas, but MMRG mutations may be relevant for the assessment of tumor characteristics and patients' prognosis. Therefore, we investigated the relationship between expression of MMRG, tumor biology and patients' survival. In 127 patients with sporadic colorectal carcinomas and a minimum of 5 years follow-up after curative surgery immunohistochemical detection of MLHI and MSH2 was analyzed semiquantitatively. Lost expression of MLHI has been found in tumor specimens from 10 patients, whereas MSH2 expression was missing in 5 patients. This reduced expression did not correlate with tumor stage, lymph node involvement, grading or tumor invasion into blood vessels. However, a significant correlation was found for lymphovascular invasion (P = 0.02) and localization within the colorectum (P = 0.003) in MLH1-negative carcinomas. In addition, although there was a clear tendency for longer overall survival (72 vs. 63 months) for patients with MLH1-negative carcinomas, significant differences for overall and recurrence-free survival were not seen. In conclusion of our results and a critical review of literature, the prognostic importance of the MMR genes in sporadic colorectal carcinomas remains controversial.

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Year:  2002        PMID: 11918085     DOI: 10.1023/a:1013853224644

Source DB:  PubMed          Journal:  Clin Exp Metastasis        ISSN: 0262-0898            Impact factor:   5.150


  48 in total

1.  Microsatellite Instability and hMLH1 and hMSH2 expression analysis in familial and sporadic colorectal cancer.

Authors:  S Salahshor; K Koelble; C Rubio; A Lindblom
Journal:  Lab Invest       Date:  2001-04       Impact factor: 5.662

2.  Choice of management strategy for colorectal cancer based on a diagnostic immunohistochemical test for defective mismatch repair.

Authors:  L Cawkwell; S Gray; H Murgatroyd; F Sutherland; L Haine; M Longfellow; S O'Loughlin; D Cross; O Kronborg; C Fenger; N Mapstone; M Dixon; P Quirke
Journal:  Gut       Date:  1999-09       Impact factor: 23.059

3.  Microsatellite instability and p53 mutations in sporadic right and left colon carcinoma: different clinical and molecular implications.

Authors:  M E Lleonart; J García-Foncillas; R Sánchez-Prieto; P Martín; A Moreno; C Salas; S Ramón y Cajal
Journal:  Cancer       Date:  1998-09-01       Impact factor: 6.860

4.  Microsatellite instability and the role of hMSH2 in sporadic colorectalcancer.

Authors:  V J Bubb; L J Curtis; C Cunningham; M G Dunlop; A D Carothers; R G Morris; S White; C C Bird; A H Wyllie
Journal:  Oncogene       Date:  1996-06-20       Impact factor: 9.867

5.  Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability.

Authors:  K K Herfarth; I J Kodner; A J Whelan; J L Ivanovich; J R Bracamontes; S A Wells; P J Goodfellow
Journal:  Genes Chromosomes Cancer       Date:  1997-01       Impact factor: 5.006

6.  Clinical and pathological characteristics of sporadic colorectal carcinomas with DNA replication errors in microsatellite sequences.

Authors:  H Kim; J Jen; B Vogelstein; S R Hamilton
Journal:  Am J Pathol       Date:  1994-07       Impact factor: 4.307

Review 7.  A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer.

Authors:  C R Boland; S N Thibodeau; S R Hamilton; D Sidransky; J R Eshleman; R W Burt; S J Meltzer; M A Rodriguez-Bigas; R Fodde; G N Ranzani; S Srivastava
Journal:  Cancer Res       Date:  1998-11-15       Impact factor: 12.701

8.  Expression of the mismatch repair gene hMSH2 in sporadic colorectal cancer.

Authors:  K Maeda; Y Nishiguchi; N Onoda; H Otani; B Nakata; S Yamada; M Okuno; M Sowa; K H Chung
Journal:  Int J Oncol       Date:  1998-12       Impact factor: 5.650

9.  Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients.

Authors:  L A Aaltonen; P Peltomäki; J P Mecklin; H Järvinen; J R Jass; J S Green; H T Lynch; P Watson; G Tallqvist; M Juhola
Journal:  Cancer Res       Date:  1994-04-01       Impact factor: 12.701

10.  Extensive molecular screening for hereditary non-polyposis colorectal cancer.

Authors:  B Dieumegard; S Grandjouan; J C Sabourin; M L Le Bihan; I Lefrère; J P Pignon; P Rougier; P Lasser; J Bénard; D Couturier; B Bressac-de Paillerets
Journal:  Br J Cancer       Date:  2000-02       Impact factor: 7.640

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  5 in total

1.  Loss of hMSH2 gene expression correlates with improved survival in patients with sporadic colorectal cancer.

Authors:  Ewa Langner; Karolina Przybylowska; Radzislaw Trzcinski; Michal Mik; Przemyslaw Galbfach; Beata Smolarz; Hanna Romanowicz-Makowska; Janusz Smigileski; Andrzej Kulig; Adam Dziki
Journal:  J Genet       Date:  2010-04       Impact factor: 1.166

2.  MLH1 as a direct target of MiR-155 and a potential predictor of favorable prognosis in pancreatic cancer.

Authors:  Wen-Jing Liu; Yu-Pei Zhao; Tai-Ping Zhang; Li Zhou; Quan-Cai Cui; Wei-Xun Zhou; Lei You; Ge Chen; Hong Shu
Journal:  J Gastrointest Surg       Date:  2013-05-29       Impact factor: 3.452

3.  Human mutL homolog 1 expression characteristic and prognostic effect on patients with sporadic colorectal cancer.

Authors:  Chibin Pu; Weiguo Ren; Zhenqiang Sun; Xianbo Yu; Wei Yuan; Mingyu Huang; Shourong Shen; Xiaoyan Wang
Journal:  Int J Clin Exp Med       Date:  2015-10-15

4.  Importance of MutL homologue MLH1 and MutS homologue MSH2 expression in Turkish patients with sporadic colorectal cancer.

Authors:  Sibel Erdamar; Esra Ucaryilmaz; Gokhan Demir; Tayfun Karahasanoglu; Gulen Dogusoy; Ahmet Dirican; Suha Goksel
Journal:  World J Gastroenterol       Date:  2007-09-07       Impact factor: 5.742

5.  Low expression of MSH2 DNA repair protein is associated with poor prognosis in head and neck squamous cell carcinoma.

Authors:  Camila Santos Pereira; Marcos Vinícius Macedo de Oliveira; Lucas Oliveira Barros; Gabriela Alencar Bandeira; Sérgio Henrique Sousa Santos; John R Basile; André Luiz Sena Guimarães; Alfredo Maurício Batista De Paula
Journal:  J Appl Oral Sci       Date:  2013 Sep-Oct       Impact factor: 2.698

  5 in total

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