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Hyperplastic Polyps Are Innocuous Lesions in Hereditary Nonpolyposis Colorectal Cancers

Aims. To compare methylation profiles, protein expression, and microsatellite instability (MSI) of sporadic, HNPCC, and familial hyperplastic polyps (HPs). Methods. Methylation-specific PCR (MSP) and pyrosequencing assessed p16, MGMT, hMLH-1, MINT 1, and MINT 31 methylation. IHC (Immunohistochemistr...

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Autores principales: Speake, D., O'Sullivan, J., Evans, D. G., Lalloo, F., Hill, J., McMahon, R. F. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263654/
https://www.ncbi.nlm.nih.gov/pubmed/22312515
http://dx.doi.org/10.1155/2011/653163
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author Speake, D.
O'Sullivan, J.
Evans, D. G.
Lalloo, F.
Hill, J.
McMahon, R. F. T.
author_facet Speake, D.
O'Sullivan, J.
Evans, D. G.
Lalloo, F.
Hill, J.
McMahon, R. F. T.
author_sort Speake, D.
collection PubMed
description Aims. To compare methylation profiles, protein expression, and microsatellite instability (MSI) of sporadic, HNPCC, and familial hyperplastic polyps (HPs). Methods. Methylation-specific PCR (MSP) and pyrosequencing assessed p16, MGMT, hMLH-1, MINT 1, and MINT 31 methylation. IHC (Immunohistochemistry) assessed Ki67, CK20, hMLH-1, hMSH-2, and hMSH-6 protein expression. MSI analysis was performed on those polyps with adequate DNA remaining. Results. 124 HPs were identified 78 sporadic, 21 HNPCC, 25 familial, and the HNPCC group demonstrated no significant differences in overall methylation (P = .186 Chi(2)). The familial group demonstrated significantly less over all methylation levels (P = .004 Chi(2)). Conclusions. HPs that occur in HNPCC have no more worrying features at a molecular level than those patients with HPs in a sporadic setting.
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spelling pubmed-32636542012-02-06 Hyperplastic Polyps Are Innocuous Lesions in Hereditary Nonpolyposis Colorectal Cancers Speake, D. O'Sullivan, J. Evans, D. G. Lalloo, F. Hill, J. McMahon, R. F. T. Int J Surg Oncol Research Article Aims. To compare methylation profiles, protein expression, and microsatellite instability (MSI) of sporadic, HNPCC, and familial hyperplastic polyps (HPs). Methods. Methylation-specific PCR (MSP) and pyrosequencing assessed p16, MGMT, hMLH-1, MINT 1, and MINT 31 methylation. IHC (Immunohistochemistry) assessed Ki67, CK20, hMLH-1, hMSH-2, and hMSH-6 protein expression. MSI analysis was performed on those polyps with adequate DNA remaining. Results. 124 HPs were identified 78 sporadic, 21 HNPCC, 25 familial, and the HNPCC group demonstrated no significant differences in overall methylation (P = .186 Chi(2)). The familial group demonstrated significantly less over all methylation levels (P = .004 Chi(2)). Conclusions. HPs that occur in HNPCC have no more worrying features at a molecular level than those patients with HPs in a sporadic setting. Hindawi Publishing Corporation 2011 2011-06-07 /pmc/articles/PMC3263654/ /pubmed/22312515 http://dx.doi.org/10.1155/2011/653163 Text en Copyright © 2011 D. Speake et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Speake, D.
O'Sullivan, J.
Evans, D. G.
Lalloo, F.
Hill, J.
McMahon, R. F. T.
Hyperplastic Polyps Are Innocuous Lesions in Hereditary Nonpolyposis Colorectal Cancers
title Hyperplastic Polyps Are Innocuous Lesions in Hereditary Nonpolyposis Colorectal Cancers
title_full Hyperplastic Polyps Are Innocuous Lesions in Hereditary Nonpolyposis Colorectal Cancers
title_fullStr Hyperplastic Polyps Are Innocuous Lesions in Hereditary Nonpolyposis Colorectal Cancers
title_full_unstemmed Hyperplastic Polyps Are Innocuous Lesions in Hereditary Nonpolyposis Colorectal Cancers
title_short Hyperplastic Polyps Are Innocuous Lesions in Hereditary Nonpolyposis Colorectal Cancers
title_sort hyperplastic polyps are innocuous lesions in hereditary nonpolyposis colorectal cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263654/
https://www.ncbi.nlm.nih.gov/pubmed/22312515
http://dx.doi.org/10.1155/2011/653163
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