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Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases

Diabetes is an established risk factor for colorectal cancer. However, colorectal cancer is a heterogeneous disease and it is not well understood whether diabetes is more strongly associated with some tumor molecular subtypes than others. A better understanding of the association between diabetes an...

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Autores principales: Harlid, Sophia, Van Guelpen, Bethany, Qu, Conghui, Gylling, Björn, Aglago, Elom K., Amitay, Efrat L., Brenner, Hermann, Buchanan, Daniel D., Campbell, Peter T., Cao, Yin, Chan, Andrew T., Chang‐Claude, Jenny, Drew, David A., Figueiredo, Jane C., French, Amy J., Gallinger, Steven, Giannakis, Marios, Giles, Graham G., Gunter, Marc J., Hoffmeister, Michael, Hsu, Li, Jenkins, Mark A., Lin, Yi, Moreno, Victor, Murphy, Neil, Newcomb, Polly A., Newton, Christina C., Nowak, Jonathan A., Obón‐Santacana, Mireia, Ogino, Shuji, Potter, John D., Song, Mingyang, Steinfelder, Robert S., Sun, Wei, Thibodeau, Stephen N., Toland, Amanda E., Ugai, Tomotaka, Um, Caroline Y., Woods, Michael O., Phipps, Amanda I., Harrison, Tabitha, Peters, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251811/
https://www.ncbi.nlm.nih.gov/pubmed/35383926
http://dx.doi.org/10.1002/ijc.34015
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author Harlid, Sophia
Van Guelpen, Bethany
Qu, Conghui
Gylling, Björn
Aglago, Elom K.
Amitay, Efrat L.
Brenner, Hermann
Buchanan, Daniel D.
Campbell, Peter T.
Cao, Yin
Chan, Andrew T.
Chang‐Claude, Jenny
Drew, David A.
Figueiredo, Jane C.
French, Amy J.
Gallinger, Steven
Giannakis, Marios
Giles, Graham G.
Gunter, Marc J.
Hoffmeister, Michael
Hsu, Li
Jenkins, Mark A.
Lin, Yi
Moreno, Victor
Murphy, Neil
Newcomb, Polly A.
Newton, Christina C.
Nowak, Jonathan A.
Obón‐Santacana, Mireia
Ogino, Shuji
Potter, John D.
Song, Mingyang
Steinfelder, Robert S.
Sun, Wei
Thibodeau, Stephen N.
Toland, Amanda E.
Ugai, Tomotaka
Um, Caroline Y.
Woods, Michael O.
Phipps, Amanda I.
Harrison, Tabitha
Peters, Ulrike
author_facet Harlid, Sophia
Van Guelpen, Bethany
Qu, Conghui
Gylling, Björn
Aglago, Elom K.
Amitay, Efrat L.
Brenner, Hermann
Buchanan, Daniel D.
Campbell, Peter T.
Cao, Yin
Chan, Andrew T.
Chang‐Claude, Jenny
Drew, David A.
Figueiredo, Jane C.
French, Amy J.
Gallinger, Steven
Giannakis, Marios
Giles, Graham G.
Gunter, Marc J.
Hoffmeister, Michael
Hsu, Li
Jenkins, Mark A.
Lin, Yi
Moreno, Victor
Murphy, Neil
Newcomb, Polly A.
Newton, Christina C.
Nowak, Jonathan A.
Obón‐Santacana, Mireia
Ogino, Shuji
Potter, John D.
Song, Mingyang
Steinfelder, Robert S.
Sun, Wei
Thibodeau, Stephen N.
Toland, Amanda E.
Ugai, Tomotaka
Um, Caroline Y.
Woods, Michael O.
Phipps, Amanda I.
Harrison, Tabitha
Peters, Ulrike
author_sort Harlid, Sophia
collection PubMed
description Diabetes is an established risk factor for colorectal cancer. However, colorectal cancer is a heterogeneous disease and it is not well understood whether diabetes is more strongly associated with some tumor molecular subtypes than others. A better understanding of the association between diabetes and colorectal cancer according to molecular subtypes could provide important insights into the biology of this association. We used data on lifestyle and clinical characteristics from the Colorectal Cancer Family Registry (CCFR) and the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO), including 9756 colorectal cancer cases (with tumor marker data) and 9985 controls, to evaluate associations between reported diabetes and risk of colorectal cancer according to molecular subtypes. Tumor markers included BRAF and KRAS mutations, microsatellite instability and CpG island methylator phenotype. In the multinomial logistic regression model, comparing colorectal cancer cases to cancer‐free controls, diabetes was positively associated with colorectal cancer regardless of subtype. The highest OR estimate was found for BRAF‐mutated colorectal cancer, n = 1086 (OR(fully adj): 1.67, 95% confidence intervals [CI]: 1.36‐2.05), with an attenuated association observed between diabetes and colorectal cancer without BRAF‐mutations, n = 7959 (OR(fully adj): 1.33, 95% CI: 1.19‐1.48). In the case only analysis, BRAF‐mutation was differentially associated with diabetes (P (difference) = .03). For the other markers, associations with diabetes were similar across tumor subtypes. In conclusion, our study confirms the established association between diabetes and colorectal cancer risk, and suggests that it particularly increases the risk of BRAF‐mutated tumors.
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spelling pubmed-92518112022-10-14 Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases Harlid, Sophia Van Guelpen, Bethany Qu, Conghui Gylling, Björn Aglago, Elom K. Amitay, Efrat L. Brenner, Hermann Buchanan, Daniel D. Campbell, Peter T. Cao, Yin Chan, Andrew T. Chang‐Claude, Jenny Drew, David A. Figueiredo, Jane C. French, Amy J. Gallinger, Steven Giannakis, Marios Giles, Graham G. Gunter, Marc J. Hoffmeister, Michael Hsu, Li Jenkins, Mark A. Lin, Yi Moreno, Victor Murphy, Neil Newcomb, Polly A. Newton, Christina C. Nowak, Jonathan A. Obón‐Santacana, Mireia Ogino, Shuji Potter, John D. Song, Mingyang Steinfelder, Robert S. Sun, Wei Thibodeau, Stephen N. Toland, Amanda E. Ugai, Tomotaka Um, Caroline Y. Woods, Michael O. Phipps, Amanda I. Harrison, Tabitha Peters, Ulrike Int J Cancer Cancer Epidemiology Diabetes is an established risk factor for colorectal cancer. However, colorectal cancer is a heterogeneous disease and it is not well understood whether diabetes is more strongly associated with some tumor molecular subtypes than others. A better understanding of the association between diabetes and colorectal cancer according to molecular subtypes could provide important insights into the biology of this association. We used data on lifestyle and clinical characteristics from the Colorectal Cancer Family Registry (CCFR) and the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO), including 9756 colorectal cancer cases (with tumor marker data) and 9985 controls, to evaluate associations between reported diabetes and risk of colorectal cancer according to molecular subtypes. Tumor markers included BRAF and KRAS mutations, microsatellite instability and CpG island methylator phenotype. In the multinomial logistic regression model, comparing colorectal cancer cases to cancer‐free controls, diabetes was positively associated with colorectal cancer regardless of subtype. The highest OR estimate was found for BRAF‐mutated colorectal cancer, n = 1086 (OR(fully adj): 1.67, 95% confidence intervals [CI]: 1.36‐2.05), with an attenuated association observed between diabetes and colorectal cancer without BRAF‐mutations, n = 7959 (OR(fully adj): 1.33, 95% CI: 1.19‐1.48). In the case only analysis, BRAF‐mutation was differentially associated with diabetes (P (difference) = .03). For the other markers, associations with diabetes were similar across tumor subtypes. In conclusion, our study confirms the established association between diabetes and colorectal cancer risk, and suggests that it particularly increases the risk of BRAF‐mutated tumors. John Wiley & Sons, Inc. 2022-04-22 2022-08-01 /pmc/articles/PMC9251811/ /pubmed/35383926 http://dx.doi.org/10.1002/ijc.34015 Text en © 2022 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Epidemiology
Harlid, Sophia
Van Guelpen, Bethany
Qu, Conghui
Gylling, Björn
Aglago, Elom K.
Amitay, Efrat L.
Brenner, Hermann
Buchanan, Daniel D.
Campbell, Peter T.
Cao, Yin
Chan, Andrew T.
Chang‐Claude, Jenny
Drew, David A.
Figueiredo, Jane C.
French, Amy J.
Gallinger, Steven
Giannakis, Marios
Giles, Graham G.
Gunter, Marc J.
Hoffmeister, Michael
Hsu, Li
Jenkins, Mark A.
Lin, Yi
Moreno, Victor
Murphy, Neil
Newcomb, Polly A.
Newton, Christina C.
Nowak, Jonathan A.
Obón‐Santacana, Mireia
Ogino, Shuji
Potter, John D.
Song, Mingyang
Steinfelder, Robert S.
Sun, Wei
Thibodeau, Stephen N.
Toland, Amanda E.
Ugai, Tomotaka
Um, Caroline Y.
Woods, Michael O.
Phipps, Amanda I.
Harrison, Tabitha
Peters, Ulrike
Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases
title Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases
title_full Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases
title_fullStr Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases
title_full_unstemmed Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases
title_short Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases
title_sort diabetes mellitus in relation to colorectal tumor molecular subtypes: a pooled analysis of more than 9000 cases
topic Cancer Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251811/
https://www.ncbi.nlm.nih.gov/pubmed/35383926
http://dx.doi.org/10.1002/ijc.34015
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