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SIRT1 in Secretory Organ Cancer

Mammalian silent information regulator 1 (SIRT1) is reported to play a role in cancers of the secretory organs, including thyroid, pancreatic endocrine, and ovarian tumors [1, 2, 3, 4]. A recent meta-analysis conducted on 37 selected studies of human cancers analyzed the correlations of overall surv...

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Autor principal: Frazzi, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165890/
https://www.ncbi.nlm.nih.gov/pubmed/30319549
http://dx.doi.org/10.3389/fendo.2018.00569
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author Frazzi, Raffaele
author_facet Frazzi, Raffaele
author_sort Frazzi, Raffaele
collection PubMed
description Mammalian silent information regulator 1 (SIRT1) is reported to play a role in cancers of the secretory organs, including thyroid, pancreatic endocrine, and ovarian tumors [1, 2, 3, 4]. A recent meta-analysis conducted on 37 selected studies of human cancers analyzed the correlations of overall survival (OS), disease-free survival (DFS) and relapse-free survival (RFS) with SIRT1 expression [5]. This study reported that SIRT1 overexpression was associated with a worse OS in liver and lung cancers, while it was not correlated with OS in breast cancer, colorectal cancer, or gastric carcinoma. Collectively, the meta-analysis revealed that an unfavorable OS was associated with SIRT1 expression for solid malignancies. Given the growing importance of this class of lysine/histone deacetylases in human endocrine malignancies, a rational and focused literature assessment is desirable in light of future clinical translations.
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spelling pubmed-61658902018-10-12 SIRT1 in Secretory Organ Cancer Frazzi, Raffaele Front Endocrinol (Lausanne) Endocrinology Mammalian silent information regulator 1 (SIRT1) is reported to play a role in cancers of the secretory organs, including thyroid, pancreatic endocrine, and ovarian tumors [1, 2, 3, 4]. A recent meta-analysis conducted on 37 selected studies of human cancers analyzed the correlations of overall survival (OS), disease-free survival (DFS) and relapse-free survival (RFS) with SIRT1 expression [5]. This study reported that SIRT1 overexpression was associated with a worse OS in liver and lung cancers, while it was not correlated with OS in breast cancer, colorectal cancer, or gastric carcinoma. Collectively, the meta-analysis revealed that an unfavorable OS was associated with SIRT1 expression for solid malignancies. Given the growing importance of this class of lysine/histone deacetylases in human endocrine malignancies, a rational and focused literature assessment is desirable in light of future clinical translations. Frontiers Media S.A. 2018-09-24 /pmc/articles/PMC6165890/ /pubmed/30319549 http://dx.doi.org/10.3389/fendo.2018.00569 Text en Copyright © 2018 Frazzi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Frazzi, Raffaele
SIRT1 in Secretory Organ Cancer
title SIRT1 in Secretory Organ Cancer
title_full SIRT1 in Secretory Organ Cancer
title_fullStr SIRT1 in Secretory Organ Cancer
title_full_unstemmed SIRT1 in Secretory Organ Cancer
title_short SIRT1 in Secretory Organ Cancer
title_sort sirt1 in secretory organ cancer
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165890/
https://www.ncbi.nlm.nih.gov/pubmed/30319549
http://dx.doi.org/10.3389/fendo.2018.00569
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