Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden

Abstract Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder that predisposes to predominantly colorectal and endometrial cancers due to germline mutations in DNA mismatch repair genes, mainly MLH1 , MSH2 and in families with excess endometrial cancer also MSH6 . In t...

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Published in:International Journal of Cancer
Main Authors: Cederquist, Kristina, Emanuelsson, Monica, Göransson, Ingela, Holinski‐Feder, Elke, Müller‐Koch, Yvonne, Golovleva, Irina, Grönberg, Henrik
Other Authors: Lions Cancer Foundation at the Department of Oncology, Umeå University
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2004
Subjects:
Online Access:http://dx.doi.org/10.1002/ijc.11718
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spelling crwiley:10.1002/ijc.11718 2024-06-02T08:12:13+00:00 Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden Cederquist, Kristina Emanuelsson, Monica Göransson, Ingela Holinski‐Feder, Elke Müller‐Koch, Yvonne Golovleva, Irina Grönberg, Henrik Lions Cancer Foundation at the Department of Oncology, Umeå University 2004 http://dx.doi.org/10.1002/ijc.11718 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fijc.11718 https://onlinelibrary.wiley.com/doi/pdf/10.1002/ijc.11718 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor International Journal of Cancer volume 109, issue 3, page 370-376 ISSN 0020-7136 1097-0215 journal-article 2004 crwiley https://doi.org/10.1002/ijc.11718 2024-05-03T10:35:45Z Abstract Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder that predisposes to predominantly colorectal and endometrial cancers due to germline mutations in DNA mismatch repair genes, mainly MLH1 , MSH2 and in families with excess endometrial cancer also MSH6 . In this population‐based study, we analysed the mutation spectrum of the MLH1 , MSH2 and MSH6 genes in a cohort of patients with microsatellite unstable double primary tumours of the colorectum and the endometrium by PCR, DHPLC and sequencing. Fourteen of the 23 patients (61%) had sequence variants in MLH1 , MSH2 or MSH6 that likely affect the protein function. A majority (10/14) of the mutations was found among probands diagnosed before age 50. Five of the mutations (36%) were located in MLH1 , 3 (21%) in MSH2 and 6 (43%) in MSH6 . MSH6 seem to have larger impact in our population than in other populations, due to a founder effect since all of the MSH6 families originate from the same geographical area. MSH6 mutation carriers have later age of onset of both colorectal cancer (62 vs . 51 years) and endometrial cancer (58 vs . 48 years) and a larger proportion of endometrial cancer than MLH1 or MSH2 mutation carriers. We can conclude that patients with microsatellite unstable double primary cancers of the colorectum and the endometrium have a very high risk of carrying a mutation not only in MLH1 or MSH2 but also in MSH6 , especially if they get their first cancer diagnosis before the age of 50. © 2004 Wiley‐Liss, Inc. Article in Journal/Newspaper Northern Sweden Wiley Online Library International Journal of Cancer 109 3 370 376
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder that predisposes to predominantly colorectal and endometrial cancers due to germline mutations in DNA mismatch repair genes, mainly MLH1 , MSH2 and in families with excess endometrial cancer also MSH6 . In this population‐based study, we analysed the mutation spectrum of the MLH1 , MSH2 and MSH6 genes in a cohort of patients with microsatellite unstable double primary tumours of the colorectum and the endometrium by PCR, DHPLC and sequencing. Fourteen of the 23 patients (61%) had sequence variants in MLH1 , MSH2 or MSH6 that likely affect the protein function. A majority (10/14) of the mutations was found among probands diagnosed before age 50. Five of the mutations (36%) were located in MLH1 , 3 (21%) in MSH2 and 6 (43%) in MSH6 . MSH6 seem to have larger impact in our population than in other populations, due to a founder effect since all of the MSH6 families originate from the same geographical area. MSH6 mutation carriers have later age of onset of both colorectal cancer (62 vs . 51 years) and endometrial cancer (58 vs . 48 years) and a larger proportion of endometrial cancer than MLH1 or MSH2 mutation carriers. We can conclude that patients with microsatellite unstable double primary cancers of the colorectum and the endometrium have a very high risk of carrying a mutation not only in MLH1 or MSH2 but also in MSH6 , especially if they get their first cancer diagnosis before the age of 50. © 2004 Wiley‐Liss, Inc.
author2 Lions Cancer Foundation at the Department of Oncology, Umeå University
format Article in Journal/Newspaper
author Cederquist, Kristina
Emanuelsson, Monica
Göransson, Ingela
Holinski‐Feder, Elke
Müller‐Koch, Yvonne
Golovleva, Irina
Grönberg, Henrik
spellingShingle Cederquist, Kristina
Emanuelsson, Monica
Göransson, Ingela
Holinski‐Feder, Elke
Müller‐Koch, Yvonne
Golovleva, Irina
Grönberg, Henrik
Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden
author_facet Cederquist, Kristina
Emanuelsson, Monica
Göransson, Ingela
Holinski‐Feder, Elke
Müller‐Koch, Yvonne
Golovleva, Irina
Grönberg, Henrik
author_sort Cederquist, Kristina
title Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden
title_short Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden
title_full Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden
title_fullStr Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden
title_full_unstemmed Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden
title_sort mutation analysis of the mlh1, msh2 and msh6 genes in patients with double primary cancers of the colorectum and the endometrium: a population‐based study in northern sweden
publisher Wiley
publishDate 2004
url http://dx.doi.org/10.1002/ijc.11718
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fijc.11718
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ijc.11718
genre Northern Sweden
genre_facet Northern Sweden
op_source International Journal of Cancer
volume 109, issue 3, page 370-376
ISSN 0020-7136 1097-0215
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/ijc.11718
container_title International Journal of Cancer
container_volume 109
container_issue 3
container_start_page 370
op_container_end_page 376
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