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Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease

Colorectal cancer (CRC) is a public health problem worldwide and in Jordan. Statins are cholesterol lowering agents. Beyond their effects, statins use has been reported to reduced risk of several malignances, including CRC. This study aimed to assess the effect of statins on CRC by studying cellular...

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Autores principales: Al-Husein, Belal A., Dawah, Bara’, Bani-Hani, Saleem, Al Bashir, Samir M., Al-Sawalmeh, Khaled M., Ayoub, Nehad M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254666/
https://www.ncbi.nlm.nih.gov/pubmed/30515267
http://dx.doi.org/10.18632/oncotarget.26293
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author Al-Husein, Belal A.
Dawah, Bara’
Bani-Hani, Saleem
Al Bashir, Samir M.
Al-Sawalmeh, Khaled M.
Ayoub, Nehad M.
author_facet Al-Husein, Belal A.
Dawah, Bara’
Bani-Hani, Saleem
Al Bashir, Samir M.
Al-Sawalmeh, Khaled M.
Ayoub, Nehad M.
author_sort Al-Husein, Belal A.
collection PubMed
description Colorectal cancer (CRC) is a public health problem worldwide and in Jordan. Statins are cholesterol lowering agents. Beyond their effects, statins use has been reported to reduced risk of several malignances, including CRC. This study aimed to assess the effect of statins on CRC by studying cellular infiltration of Regulatory T Lymphocytes (Tregs) into CRC tissues and their effect on Transforming growth factor beta 1 (TGF-β(1)) level and on angiogenesis. Fourty seven specimens (25 statins users vs. 22 non-users) were used. Immunohistochemistry was performed to study Tregs infiltration using their marker, fork head transcription factor, and angiogenesis using CD31 as a marker. TGF-β(1) levels were measured using ELISA. Results revealed that statins use was associated with more Tregs infiltration, less angiogenesis but no difference in TGF-β(1) content in tumor tissue. When results were further stratified according to stage of disease, more Tregs infiltration was significantly noticed in advanced disease but not in early disease. In addition, more angiogenesis inhibition was noticed in early disease but not in advanced disease. Same stage-dependence wasn’t noticed with TGF-β(1) expression. In early disease, reduction of angiogenesis mediated by statins might lead to reduction of tumor aggressiveness. On the other hand, Tregs infiltration into tumor mediated by statins might reduce cancer aggressiveness in advanced disease. These results suggest that statins might be used in the treatment of CRC.
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spelling pubmed-62546662018-12-04 Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease Al-Husein, Belal A. Dawah, Bara’ Bani-Hani, Saleem Al Bashir, Samir M. Al-Sawalmeh, Khaled M. Ayoub, Nehad M. Oncotarget Research Paper Colorectal cancer (CRC) is a public health problem worldwide and in Jordan. Statins are cholesterol lowering agents. Beyond their effects, statins use has been reported to reduced risk of several malignances, including CRC. This study aimed to assess the effect of statins on CRC by studying cellular infiltration of Regulatory T Lymphocytes (Tregs) into CRC tissues and their effect on Transforming growth factor beta 1 (TGF-β(1)) level and on angiogenesis. Fourty seven specimens (25 statins users vs. 22 non-users) were used. Immunohistochemistry was performed to study Tregs infiltration using their marker, fork head transcription factor, and angiogenesis using CD31 as a marker. TGF-β(1) levels were measured using ELISA. Results revealed that statins use was associated with more Tregs infiltration, less angiogenesis but no difference in TGF-β(1) content in tumor tissue. When results were further stratified according to stage of disease, more Tregs infiltration was significantly noticed in advanced disease but not in early disease. In addition, more angiogenesis inhibition was noticed in early disease but not in advanced disease. Same stage-dependence wasn’t noticed with TGF-β(1) expression. In early disease, reduction of angiogenesis mediated by statins might lead to reduction of tumor aggressiveness. On the other hand, Tregs infiltration into tumor mediated by statins might reduce cancer aggressiveness in advanced disease. These results suggest that statins might be used in the treatment of CRC. Impact Journals LLC 2018-11-06 /pmc/articles/PMC6254666/ /pubmed/30515267 http://dx.doi.org/10.18632/oncotarget.26293 Text en Copyright: © 2018 Al-Husein et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Al-Husein, Belal A.
Dawah, Bara’
Bani-Hani, Saleem
Al Bashir, Samir M.
Al-Sawalmeh, Khaled M.
Ayoub, Nehad M.
Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease
title Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease
title_full Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease
title_fullStr Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease
title_full_unstemmed Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease
title_short Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease
title_sort immunomodulatory effect of statins on regulatory t lymphocytes in human colorectal cancer is determined by the stage of disease
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254666/
https://www.ncbi.nlm.nih.gov/pubmed/30515267
http://dx.doi.org/10.18632/oncotarget.26293
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