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The clinicopathological significance of SIRT1 expression in colon cancer: An immunohistochemical study and meta-analysis.

Authors :
Hong WG
Pyo JS
Source :
Pathology, research and practice [Pathol Res Pract] 2018 Oct; Vol. 214 (10), pp. 1550-1555. Date of Electronic Publication: 2018 Aug 01.
Publication Year :
2018

Abstract

Objective: The aim of this study was to determine the clinicopathological significance and potential prognostic role of SIRT1 expression in colorectal cancer (CRC) using immunohistochemistry and meta-analysis.<br />Methods: Immunohistochemistry was performed on 265 archival paraffin-embedded human CRC specimens to investigate the correlation between SIRT1 expression and clinicopathological characteristics, including patient survival. To elucidate the potential prognostic value of SIRT1 expression, a meta-analysis was performed using data on 2132 patients from eight eligible studies.<br />Results: SIRT1 was highly expressed in 24.5% of the 265 CRC specimens analyzed. High SIRT1 expression correlated with vascular invasion (P =  0.041). High SIRT1 expression also significantly correlated with expression of SNAI (P =  0.001), but not E-cadherin (P =  0.958). However, there was no significant correlation between SIRT1 expression and other clinicopathological parameters. High SIRT1 expression in the CRC specimens significantly correlated with a worse overall survival rate, independent of SNAI expression. However, based on the meta-analysis, high SIRT1 expression was not significantly correlated with overall survival rates [hazard ratio (HR) 1.111, 95% confidential interval (CI) 0.799-1.544].<br />Conclusion: In our retrospective study, high SIRT1 expression significantly correlated with vascular invasion and a worse prognosis. However, because the results from the meta-analysis differed the retrospective arm of our study, additional cumulative studies are needed to determine the prognostic value of SIRT1 in CRC.<br /> (Copyright © 2018. Published by Elsevier GmbH.)

Details

Language :
English
ISSN :
1618-0631
Volume :
214
Issue :
10
Database :
MEDLINE
Journal :
Pathology, research and practice
Publication Type :
Academic Journal
Accession number :
30082156
Full Text :
https://doi.org/10.1016/j.prp.2018.07.022