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Altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence

Background and Objective: Colorectal cancer (CRC) is a major health problem in developed countries. Adenomatous lesions in the large bowel are the main precursors of CRC and the adenoma-adenocarcinoma sequence still provides a solid model for research on carcinogenesis. The finding of local renin-an...

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Autores principales: Beitia, Maider, Solano-Iturri, Jon Danel, Errarte, Peio, Sanz, Begoña, Perez, Itxaro, Etxezarraga, María C., Loizate, Alberto, Asumendi, Aintzane, Larrinaga, Gorka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643103/
https://www.ncbi.nlm.nih.gov/pubmed/31337954
http://dx.doi.org/10.7150/ijms.32599
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author Beitia, Maider
Solano-Iturri, Jon Danel
Errarte, Peio
Sanz, Begoña
Perez, Itxaro
Etxezarraga, María C.
Loizate, Alberto
Asumendi, Aintzane
Larrinaga, Gorka
author_facet Beitia, Maider
Solano-Iturri, Jon Danel
Errarte, Peio
Sanz, Begoña
Perez, Itxaro
Etxezarraga, María C.
Loizate, Alberto
Asumendi, Aintzane
Larrinaga, Gorka
author_sort Beitia, Maider
collection PubMed
description Background and Objective: Colorectal cancer (CRC) is a major health problem in developed countries. Adenomatous lesions in the large bowel are the main precursors of CRC and the adenoma-adenocarcinoma sequence still provides a solid model for research on carcinogenesis. The finding of local renin-angiotensin systems (RAS) has been crucial to understand the role of this peptidergic system in cancer and has opened new perspectives in the study of colorectal carcinogenetic processes. Methods: In this study we analyzed the immunohistochemical expression of three main RAS receptors (AT1, AT2 and MAS) in a large series of CRC samples (n=161), including uninvolved intestinal mucosa-adenoma-adenocarcinoma sequences from the same patients (n=50). Results: 1) AT1 and AT2 showed a biphasic expression pattern along the sequence. The expression significantly decreased in adenomas with respect to uninvolved mucosa but increased in CRCs. 2) AT2 expression was lower in advanced CRCs with high local invasion (pT4), high stage (IV), high nodal (N2) and vascular invasion. 3) MAS receptor was moderately expressed in the uninvolved mucosa and in adenomas. This expression increased very significantly in CRC tissues. Conclusions: These results suggest that: 1) RAS receptors are differentially regulated as the genetic and epigenetic alterations accumulate throughout the uninvolved mucosa-adenoma-CRC sequence. 2) Loss of AT2 expression could contribute to the aggressive behavior of advanced CRC cells.
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spelling pubmed-66431032019-07-23 Altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence Beitia, Maider Solano-Iturri, Jon Danel Errarte, Peio Sanz, Begoña Perez, Itxaro Etxezarraga, María C. Loizate, Alberto Asumendi, Aintzane Larrinaga, Gorka Int J Med Sci Research Paper Background and Objective: Colorectal cancer (CRC) is a major health problem in developed countries. Adenomatous lesions in the large bowel are the main precursors of CRC and the adenoma-adenocarcinoma sequence still provides a solid model for research on carcinogenesis. The finding of local renin-angiotensin systems (RAS) has been crucial to understand the role of this peptidergic system in cancer and has opened new perspectives in the study of colorectal carcinogenetic processes. Methods: In this study we analyzed the immunohistochemical expression of three main RAS receptors (AT1, AT2 and MAS) in a large series of CRC samples (n=161), including uninvolved intestinal mucosa-adenoma-adenocarcinoma sequences from the same patients (n=50). Results: 1) AT1 and AT2 showed a biphasic expression pattern along the sequence. The expression significantly decreased in adenomas with respect to uninvolved mucosa but increased in CRCs. 2) AT2 expression was lower in advanced CRCs with high local invasion (pT4), high stage (IV), high nodal (N2) and vascular invasion. 3) MAS receptor was moderately expressed in the uninvolved mucosa and in adenomas. This expression increased very significantly in CRC tissues. Conclusions: These results suggest that: 1) RAS receptors are differentially regulated as the genetic and epigenetic alterations accumulate throughout the uninvolved mucosa-adenoma-CRC sequence. 2) Loss of AT2 expression could contribute to the aggressive behavior of advanced CRC cells. Ivyspring International Publisher 2019-06-02 /pmc/articles/PMC6643103/ /pubmed/31337954 http://dx.doi.org/10.7150/ijms.32599 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Beitia, Maider
Solano-Iturri, Jon Danel
Errarte, Peio
Sanz, Begoña
Perez, Itxaro
Etxezarraga, María C.
Loizate, Alberto
Asumendi, Aintzane
Larrinaga, Gorka
Altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence
title Altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence
title_full Altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence
title_fullStr Altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence
title_full_unstemmed Altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence
title_short Altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence
title_sort altered expression of renin-angiotensin system receptors throughout colorectal adenoma-adenocarcinoma sequence
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643103/
https://www.ncbi.nlm.nih.gov/pubmed/31337954
http://dx.doi.org/10.7150/ijms.32599
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