Cancer risks for MLH1 and MSH2 mutation carriers - PubMed (original) (raw)
Aung K Win, Daniel D Buchanan, Noralane M Lindor, Finlay A Macrae, Mark Clendenning, Yoland C Antill, Stephen N Thibodeau, Graham Casey, Steve Gallinger, Loic Le Marchand, Polly A Newcomb, Robert W Haile, Graeme P Young, Paul A James, Graham G Giles, Shanaka R Gunawardena, Barbara A Leggett, Michael Gattas, Alex Boussioutas, Dennis J Ahnen, John A Baron, Susan Parry, Jack Goldblatt, Joanne P Young, John L Hopper, Mark A Jenkins
Affiliations
- PMID: 23255516
- PMCID: PMC3887142
- DOI: 10.1002/humu.22262
Cancer risks for MLH1 and MSH2 mutation carriers
James G Dowty et al. Hum Mutat. 2013 Mar.
Abstract
We studied 17,576 members of 166 MLH1 and 224 MSH2 mutation-carrying families from the Colon Cancer Family Registry. Average cumulative risks of colorectal cancer (CRC), endometrial cancer (EC), and other cancers for carriers were estimated using modified segregation analysis conditioned on ascertainment criteria. Heterogeneity in risks was investigated using a polygenic risk modifier. Average CRC cumulative risks at the age of 70 years (95% confidence intervals) for MLH1 and MSH2 mutation carriers, respectively, were estimated to be 34% (25%-50%) and 47% (36%-60%) for male carriers and 36% (25%-51%) and 37% (27%-50%) for female carriers. Corresponding EC risks were 18% (9.1%-34%) and 30% (18%-45%). A high level of CRC risk heterogeneity was observed (P < 0.001), with cumulative risks at the age of 70 years estimated to follow U-shaped distributions. For example, 17% of male MSH2 mutation carriers have estimated lifetime risks of 0%-10% and 18% have risks of 90%-100%. Therefore, average risks are similar for the two genes but there is so much individual variation about the average that large proportions of carriers have either very low or very high lifetime cancer risks. Our estimates of CRC and EC cumulative risks for MLH1 and MSH2 mutation carriers are the most precise currently available.
© 2012 Wiley Periodicals, Inc.
Conflict of interest statement
The authors have no conflicts of interest to declare with respect to this manuscript.
Figures
Figure 1
The estimated distribution of colorectal cancer cumulative risk to age 70 years for each combination of gene and sex. For example, from the leftmost black bar, 17% of male MSH2 mutation carriers are estimated to have a less than 10% chance of developing colorectal cancer by age 70 years.
Figure 2
Colorectal cancer cumulative risks for males (A) and females (B) and endometrial cancer cumulative risks for females (C). Cumulative risks are for MLH1 mutation carriers (unbroken lines), MSH2 mutation carriers (dashed lines) and the general population (dotted lines) living in Australia and New Zealand (light grey), Canada (dark grey) and USA (black).
Similar articles
- Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
Bonadona V, Bonaïti B, Olschwang S, Grandjouan S, Huiart L, Longy M, Guimbaud R, Buecher B, Bignon YJ, Caron O, Colas C, Noguès C, Lejeune-Dumoulin S, Olivier-Faivre L, Polycarpe-Osaer F, Nguyen TD, Desseigne F, Saurin JC, Berthet P, Leroux D, Duffour J, Manouvrier S, Frébourg T, Sobol H, Lasset C, Bonaïti-Pellié C; French Cancer Genetics Network. Bonadona V, et al. JAMA. 2011 Jun 8;305(22):2304-10. doi: 10.1001/jama.2011.743. JAMA. 2011. PMID: 21642682 - Cumulative incidence of colorectal and extracolonic cancers in MLH1 and MSH2 mutation carriers of hereditary nonpolyposis colorectal cancer.
Lin KM, Shashidharan M, Thorson AG, Ternent CA, Blatchford GJ, Christensen MA, Watson P, Lemon SJ, Franklin B, Karr B, Lynch J, Lynch HT. Lin KM, et al. J Gastrointest Surg. 1998 Jan-Feb;2(1):67-71. doi: 10.1016/s1091-255x(98)80105-4. J Gastrointest Surg. 1998. PMID: 9841970 - Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome.
Stoffel E, Mukherjee B, Raymond VM, Tayob N, Kastrinos F, Sparr J, Wang F, Bandipalliam P, Syngal S, Gruber SB. Stoffel E, et al. Gastroenterology. 2009 Nov;137(5):1621-7. doi: 10.1053/j.gastro.2009.07.039. Epub 2009 Jul 18. Gastroenterology. 2009. PMID: 19622357 Free PMC article. - Risk Factors Associated with Colorectal Cancer in a Subset of Patients with Mutations in MLH1 and MSH2 in Taiwan Fulfilling the Amsterdam II Criteria for Lynch Syndrome.
Kamiza AB, Hsieh LL, Tang R, Chien HT, Lai CH, Chiu LL, Lo TP, Hung KY, Wang CY, You JF, Hsiung CA, Yeh CC. Kamiza AB, et al. PLoS One. 2015 Jun 8;10(6):e0130018. doi: 10.1371/journal.pone.0130018. eCollection 2015. PLoS One. 2015. PMID: 26053027 Free PMC article. - Phenotype comparison of MLH1 and MSH2 mutation carriers in a cohort of 1,914 individuals undergoing clinical genetic testing in the United States.
Kastrinos F, Stoffel EM, Balmaña J, Steyerberg EW, Mercado R, Syngal S. Kastrinos F, et al. Cancer Epidemiol Biomarkers Prev. 2008 Aug;17(8):2044-51. doi: 10.1158/1055-9965.EPI-08-0301. Cancer Epidemiol Biomarkers Prev. 2008. PMID: 18708397
Cited by
- Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?
Win AK, Hopper JL, Buchanan DD, Young JP, Tenesa A, Dowty JG, Giles GG, Goldblatt J, Winship I, Boussioutas A, Young GP, Parry S, Baron JA, Duggan D, Gallinger S, Newcomb PA, Haile RW, Le Marchand L, Lindor NM, Jenkins MA. Win AK, et al. Eur J Cancer. 2013 May;49(7):1578-87. doi: 10.1016/j.ejca.2013.01.029. Epub 2013 Feb 22. Eur J Cancer. 2013. PMID: 23434150 Free PMC article. - Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients.
Jansen AM, Geilenkirchen MA, van Wezel T, Jagmohan-Changur SC, Ruano D, van der Klift HM, van den Akker BE, Laros JF, van Galen M, Wagner A, Letteboer TG, Gómez-García EB, Tops CM, Vasen HF, Devilee P, Hes FJ, Morreau H, Wijnen JT. Jansen AM, et al. PLoS One. 2016 Jun 14;11(6):e0157381. doi: 10.1371/journal.pone.0157381. eCollection 2016. PLoS One. 2016. PMID: 27300758 Free PMC article. - Japan Society of Clinical Oncology provisional clinical opinion for the diagnosis and use of immunotherapy in patients with deficient DNA mismatch repair tumors, cooperated by Japanese Society of Medical Oncology, First Edition.
Mishima S, Taniguchi H, Akagi K, Baba E, Fujiwara Y, Hirasawa A, Ikeda M, Maeda O, Muro K, Nishihara H, Nishiyama H, Takano T, Tsuchihara K, Yatabe Y, Kodera Y, Yoshino T. Mishima S, et al. Int J Clin Oncol. 2020 Feb;25(2):217-239. doi: 10.1007/s10147-019-01498-8. Epub 2019 Jul 8. Int J Clin Oncol. 2020. PMID: 31286289 Free PMC article. - Polymorphism of DNA repair genes in breast cancer.
Smolarz B, Michalska MM, Samulak D, Romanowicz H, Wójcik L. Smolarz B, et al. Oncotarget. 2019 Jan 11;10(4):527-535. doi: 10.18632/oncotarget.26568. eCollection 2019 Jan 11. Oncotarget. 2019. PMID: 30728902 Free PMC article. - Cohort Profile: The Colon Cancer Family Registry Cohort (CCFRC).
Jenkins MA, Win AK, Templeton AS, Angelakos MS, Buchanan DD, Cotterchio M, Figueiredo JC, Thibodeau SN, Baron JA, Potter JD, Hopper JL, Casey G, Gallinger S, Le Marchand L, Lindor NM, Newcomb PA, Haile RW; Colon Cancer Family Registry Cohort Investigators. Jenkins MA, et al. Int J Epidemiol. 2018 Apr 1;47(2):387-388i. doi: 10.1093/ije/dyy006. Int J Epidemiol. 2018. PMID: 29490034 Free PMC article. No abstract available.
References
- Aaltonen LA, Sankila R, Mecklin JP, Jarvinen H, Pukkala E, Peltomaki P, de la Chapelle A. A novel approach to estimate the proportion of hereditary nonpolyposis colorectal cancer of total colorectal cancer burden. Cancer Detect Prev. 1994;18:57–63. - PubMed
- Antoniou AC, Pharoah PD, McMullan G, Day NE, Ponder BA, Easton D. Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study. Genet Epidemiol. 2001;21:1–18. - PubMed
- Barnetson RA, Tenesa A, Farrington SM, Nicholl ID, Cetnarskyj R, Porteous ME, Campbell H, Dunlop MG. Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. N Engl J Med. 2006;354:2751–63. - PubMed
- Botma A, Nagengast FM, Braem MG, Hendriks JC, Kleibeuker JH, Vasen HF, Kampman E. Body mass index increases risk of colorectal adenomas in men with Lynch syndrome: the GEOLynch cohort study. J Clin Oncol. 2010;28:4346–53. - PubMed
- Campbell PT, Edwards L, McLaughlin JR, Green J, Younghusband HB, Woods MO. Cytochrome P450 17A1 and catechol O-methyltransferase polymorphisms and age at Lynch syndrome colon cancer onset in Newfoundland. Clin Cancer Res. 2007;13:3783–8. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- U01 CA074799/CA/NCI NIH HHS/United States
- U24 CA074783/CA/NCI NIH HHS/United States
- U01 CA069398/CA/NCI NIH HHS/United States
- U24 CA074794/CA/NCI NIH HHS/United States
- U24 CA074806/CA/NCI NIH HHS/United States
- R01 CA128978/CA/NCI NIH HHS/United States
- P50 CA116201/CA/NCI NIH HHS/United States
- U01 CA069631/CA/NCI NIH HHS/United States
- U01 CA097735/CA/NCI NIH HHS/United States
- K05 CA152715/CA/NCI NIH HHS/United States
- U01 CA074783/CA/NCI NIH HHS/United States
- U01 CA074800/CA/NCI NIH HHS/United States
- U24 CA097735/CA/NCI NIH HHS/United States
- U01 CA074794/CA/NCI NIH HHS/United States
- CA-95-011/CA/NCI NIH HHS/United States
- R01 CA122340/CA/NCI NIH HHS/United States
- K22 CA095011/CA/NCI NIH HHS/United States
- U24 CA074799/CA/NCI NIH HHS/United States
- U01 CA074806/CA/NCI NIH HHS/United States
- U24 CA074800/CA/NCI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical