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Serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis

In the past two decades, besides conventional adenoma pathway, a subset of colonic lesions, including hyperplastic polyps, sessile serrated adenoma/polyps, and traditional serrated adenomas have been suggested as precancerous lesions via the alternative serrated neoplasia pathway. Major molecular al...

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Detalles Bibliográficos
Autores principales: Kim, Soon Young, Kim, Tae Il
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association for the Study of Intestinal Diseases 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077295/
https://www.ncbi.nlm.nih.gov/pubmed/30090034
http://dx.doi.org/10.5217/ir.2018.16.3.358
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author Kim, Soon Young
Kim, Tae Il
author_facet Kim, Soon Young
Kim, Tae Il
author_sort Kim, Soon Young
collection PubMed
description In the past two decades, besides conventional adenoma pathway, a subset of colonic lesions, including hyperplastic polyps, sessile serrated adenoma/polyps, and traditional serrated adenomas have been suggested as precancerous lesions via the alternative serrated neoplasia pathway. Major molecular alterations of sessile serrated neoplasia include BRAF mutation, high CpG island methylator phenotype, and escape of cellular senescence and progression via methylation of tumor suppressor genes or mismatch repair genes. With increasing information of the morphologic and molecular features of serrated lesions, one major challenge is how to reflect this knowledge in clinical practice, such as pathologic and endoscopic diagnosis, and guidelines for treatment and surveillance.
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spelling pubmed-60772952018-08-08 Serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis Kim, Soon Young Kim, Tae Il Intest Res Focused Review: Colorectal Cancer In the past two decades, besides conventional adenoma pathway, a subset of colonic lesions, including hyperplastic polyps, sessile serrated adenoma/polyps, and traditional serrated adenomas have been suggested as precancerous lesions via the alternative serrated neoplasia pathway. Major molecular alterations of sessile serrated neoplasia include BRAF mutation, high CpG island methylator phenotype, and escape of cellular senescence and progression via methylation of tumor suppressor genes or mismatch repair genes. With increasing information of the morphologic and molecular features of serrated lesions, one major challenge is how to reflect this knowledge in clinical practice, such as pathologic and endoscopic diagnosis, and guidelines for treatment and surveillance. Korean Association for the Study of Intestinal Diseases 2018-07 2018-07-27 /pmc/articles/PMC6077295/ /pubmed/30090034 http://dx.doi.org/10.5217/ir.2018.16.3.358 Text en © Copyright 2018. Korean Association for the Study of Intestinal Diseases. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Focused Review: Colorectal Cancer
Kim, Soon Young
Kim, Tae Il
Serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis
title Serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis
title_full Serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis
title_fullStr Serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis
title_full_unstemmed Serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis
title_short Serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis
title_sort serrated neoplasia pathway as an alternative route of colorectal cancer carcinogenesis
topic Focused Review: Colorectal Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077295/
https://www.ncbi.nlm.nih.gov/pubmed/30090034
http://dx.doi.org/10.5217/ir.2018.16.3.358
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