Evidence for an age-related influence of microsatellite instability on colorectal cancer survival - PubMed (original) (raw)
. 2002 Apr 20;98(6):844-50.
doi: 10.1002/ijc.10264.
Affiliations
- PMID: 11948461
- DOI: 10.1002/ijc.10264
Evidence for an age-related influence of microsatellite instability on colorectal cancer survival
Susan M Farrington et al. Int J Cancer. 2002.
Abstract
It is well established that microsatellite instability (MSI), the hallmark of defective DNA mismatch repair (MMR), is associated with prolonged survival in colorectal cancer compared with tumours that are microsatellite stable (MSS). MSI in sporadic colorectal tumours is primarily due to epigenetic silencing of MLH1. However, there are no prospective population-based studies of survival in patients with germline MMR gene mutations who develop cancer. Although MSI is almost universal in tumours from HNPCC family members, there is a potential confounding effect of ascertainment and other biases that could explain the apparent survival benefit in HNPCC families. Resolving whether germline MMR gene mutations impact on survival is important because it potentially undermines the rationale for surveillance of mutation carriers. Here, we report an investigation of the influence of MSI on survival in cohorts of cancer patients (aged < 30 years at diagnosis, n = 118; non-age-selected, n = 181) in the context of clinicopathologic variables. There was a substantial age-related influence of tumour MSI status on survival. In young patients with tumour MSI, 65% of patients with MSI tumours had germline MSH2 or MLH1 mutations. Clinicopathologic variables and tumour MSI of the cohort were studied with respect to survival and compared with control groups. Young patients had excess MSI tumours (p < 0.000001), mucinous tumours (p < 0.01), advanced disease (p approximately 0.001) and poorer 5-year survival compared with older cases. Cox proportional hazard analysis identified Dukes' stage, age at diagnosis and calendar year of treatment as independent predictors of survival. There was no detectable association between tumour MSI and survival in young patients, although we confirmed previous observations that MSI is associated with better prognosis in later onset cohorts. These findings underscore the rationale for surveillance and early identification of tumours in MMR gene carriers as well as refining understanding of the influence of MSI on cancer progression.
Copyright 2002 Wiley-Liss, Inc.
Similar articles
- Extended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: genetic reclassification and correlation with clinical features.
Schiemann U, Müller-Koch Y, Gross M, Daum J, Lohse P, Baretton G, Muders M, Mussack T, Kopp R, Holinski-Feder E. Schiemann U, et al. Digestion. 2004;69(3):166-76. doi: 10.1159/000078223. Epub 2004 Apr 28. Digestion. 2004. PMID: 15118395 - Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms.
Shia J, Klimstra DS, Nafa K, Offit K, Guillem JG, Markowitz AJ, Gerald WL, Ellis NA. Shia J, et al. Am J Surg Pathol. 2005 Jan;29(1):96-104. doi: 10.1097/01.pas.0000146009.85309.3b. Am J Surg Pathol. 2005. PMID: 15613860 - Immunohistochemistry and microsatellite instability testing for selecting MLH1, MSH2 and MSH6 mutation carriers in hereditary non-polyposis colorectal cancer.
Caldés T, Godino J, Sanchez A, Corbacho C, De la Hoya M, Lopez Asenjo J, Saez C, Sanz J, Benito M, Ramon Y Cajal S, Diaz-Rubio E. Caldés T, et al. Oncol Rep. 2004 Sep;12(3):621-9. Oncol Rep. 2004. PMID: 15289847 - Prognosis in DNA mismatch repair deficient colorectal cancer: are all MSI tumours equivalent?
Clark AJ, Barnetson R, Farrington SM, Dunlop MG. Clark AJ, et al. Fam Cancer. 2004;3(2):85-91. doi: 10.1023/B:FAME.0000039915.94550.cc. Fam Cancer. 2004. PMID: 15340258 Review. - The Clinical Significance of Microsatellite Instability in Precision Treatment.
Huang Z, Chen X, Liu C, Cui L. Huang Z, et al. Methods Mol Biol. 2020;2204:33-38. doi: 10.1007/978-1-0716-0904-0_3. Methods Mol Biol. 2020. PMID: 32710312 Review.
Cited by
- Distinct Molecular Profiles of Sporadic Early-Onset Colorectal Cancer: A Population-Based Cohort and Systematic Review.
Hamilton AC, Bannon FJ, Dunne PD, James J, McQuaid S, Gray RT, Salto-Tellez M, Cardwell CR, Loughrey MB, Coleman HG. Hamilton AC, et al. Gastro Hep Adv. 2022 Nov 8;2(3):347-359. doi: 10.1016/j.gastha.2022.11.005. eCollection 2023. Gastro Hep Adv. 2022. PMID: 39132649 Free PMC article. Review. - Childhood Cancer Incidence and Survival in South Australia and the Northern Territory, 1990-2017, with Emphasis on Indigenous Peoples.
Mashtoub S, Ullah S, Collinson A, Singh GR, Clark Adnyamathanha J, Leemaqz S, Paltiel O, Roder DM, Saxon B, McKinnon R, Pandol SJ, Roberts CT, Barreto SG. Mashtoub S, et al. Cancers (Basel). 2024 May 29;16(11):2057. doi: 10.3390/cancers16112057. Cancers (Basel). 2024. PMID: 38893175 Free PMC article. - Unique characteristics of the tumor immune microenvironment in young patients with metastatic colorectal cancer.
Griffith BD, Lazarus J, McGue J, Krishnan S, D'Angelica MI, Shia J, Dobrosotskaya I, Shi J, Edwards J, Rao A, Frankel TL. Griffith BD, et al. Front Immunol. 2023 Dec 13;14:1289402. doi: 10.3389/fimmu.2023.1289402. eCollection 2023. Front Immunol. 2023. PMID: 38152402 Free PMC article. - Identification of senescence-associated long non-coding RNAs to predict prognosis and immune microenvironment in patients with hepatocellular carcinoma.
Gao C, Zhou G, Cheng M, Feng L, Cao P, Zhou G. Gao C, et al. Front Genet. 2022 Oct 13;13:956094. doi: 10.3389/fgene.2022.956094. eCollection 2022. Front Genet. 2022. PMID: 36330438 Free PMC article. - Gastrointestinal Adenocarcinoma Incidence and Survival Trends in South Australia, 1990-2017.
Schell D, Ullah S, Brooke-Smith ME, Hollington P, Yeow M, Karapetis CS, Watson DI, Pandol SJ, Roberts CT, Barreto SG. Schell D, et al. Cancers (Basel). 2022 Jan 6;14(2):275. doi: 10.3390/cancers14020275. Cancers (Basel). 2022. PMID: 35053439 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical