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Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer

Ovarian cancer (OC) is the fifth most frequent cause of cancer-associated mortality worldwide, and is accompanied by asymptomatic progression. Sirtuins (SIRTs) are a family of nicotinamide adenine dinucleotide-dependent protein deacetylases, comprising seven members (SIRT1, SIRT2, SIRT3, SIRT4, SIRT...

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Autores principales: He, Qikuan, Chen, Kai, Ye, Ruifan, Dai, Ninggao, Guo, Pengyi, Wang, Leixi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074502/
https://www.ncbi.nlm.nih.gov/pubmed/32256823
http://dx.doi.org/10.3892/ol.2020.11432
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author He, Qikuan
Chen, Kai
Ye, Ruifan
Dai, Ninggao
Guo, Pengyi
Wang, Leixi
author_facet He, Qikuan
Chen, Kai
Ye, Ruifan
Dai, Ninggao
Guo, Pengyi
Wang, Leixi
author_sort He, Qikuan
collection PubMed
description Ovarian cancer (OC) is the fifth most frequent cause of cancer-associated mortality worldwide, and is accompanied by asymptomatic progression. Sirtuins (SIRTs) are a family of nicotinamide adenine dinucleotide-dependent protein deacetylases, comprising seven members (SIRT1, SIRT2, SIRT3, SIRT4, SIRT5, SIRT6 and SIRT7). Accumulating evidence has demonstrated that SIRTs act as prognostic estimators in certain types of cancer such as lung cancer, prostate cancer, gastric cancer, breast cancer and colorectal cancer. However, it remains unknown whether individual SIRTs can serve as independent prognostic factors in OC. In the present study, the Kaplan-Meier plotter online database was utilized to examine the prognostic values of SIRT mRNA expression in patients with OC. The results demonstrated that the overexpression of SIRT3, SIRT5, SIRT6 and SIRT7 mRNAs was associated with a good prognosis in patients, whereas elevated mRNA levels of SIRT1 and SIRT4 indicated poor survival in patients with OC. In addition, among the favorable predictors, SIRT3, SIRT5, SIRT6 and SIRT7 overexpression were associated with overall survival (OS), according to clinical characteristics, such as histological classification, clinical stage, pathology grade, drug therapy and tumor protein p53 mutation status in patients with OC. Similarly, SIRT4 mRNA overexpression was associated with poor OS in pathological grade III cancer. High SIRT1 and SIRT4 expression were associated with unfavorable OS at all clinical stages. Furthermore, SIRT1 and SIRT4 were negatively associated with OS in drug-treated patients. In summary, the present study demonstrated that the SIRT family is associated with the prognosis of human OC, suggesting that individual SIRTs may also act as prognostic predictors in patients.
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spelling pubmed-70745022020-03-31 Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer He, Qikuan Chen, Kai Ye, Ruifan Dai, Ninggao Guo, Pengyi Wang, Leixi Oncol Lett Articles Ovarian cancer (OC) is the fifth most frequent cause of cancer-associated mortality worldwide, and is accompanied by asymptomatic progression. Sirtuins (SIRTs) are a family of nicotinamide adenine dinucleotide-dependent protein deacetylases, comprising seven members (SIRT1, SIRT2, SIRT3, SIRT4, SIRT5, SIRT6 and SIRT7). Accumulating evidence has demonstrated that SIRTs act as prognostic estimators in certain types of cancer such as lung cancer, prostate cancer, gastric cancer, breast cancer and colorectal cancer. However, it remains unknown whether individual SIRTs can serve as independent prognostic factors in OC. In the present study, the Kaplan-Meier plotter online database was utilized to examine the prognostic values of SIRT mRNA expression in patients with OC. The results demonstrated that the overexpression of SIRT3, SIRT5, SIRT6 and SIRT7 mRNAs was associated with a good prognosis in patients, whereas elevated mRNA levels of SIRT1 and SIRT4 indicated poor survival in patients with OC. In addition, among the favorable predictors, SIRT3, SIRT5, SIRT6 and SIRT7 overexpression were associated with overall survival (OS), according to clinical characteristics, such as histological classification, clinical stage, pathology grade, drug therapy and tumor protein p53 mutation status in patients with OC. Similarly, SIRT4 mRNA overexpression was associated with poor OS in pathological grade III cancer. High SIRT1 and SIRT4 expression were associated with unfavorable OS at all clinical stages. Furthermore, SIRT1 and SIRT4 were negatively associated with OS in drug-treated patients. In summary, the present study demonstrated that the SIRT family is associated with the prognosis of human OC, suggesting that individual SIRTs may also act as prognostic predictors in patients. D.A. Spandidos 2020-04 2020-03-03 /pmc/articles/PMC7074502/ /pubmed/32256823 http://dx.doi.org/10.3892/ol.2020.11432 Text en Copyright: © He et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
He, Qikuan
Chen, Kai
Ye, Ruifan
Dai, Ninggao
Guo, Pengyi
Wang, Leixi
Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer
title Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer
title_full Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer
title_fullStr Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer
title_full_unstemmed Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer
title_short Associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer
title_sort associations of sirtuins with clinicopathological variables and prognosis in human ovarian cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074502/
https://www.ncbi.nlm.nih.gov/pubmed/32256823
http://dx.doi.org/10.3892/ol.2020.11432
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