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The correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer
We aimed to evaluate the correlation between serum sirtuin 6 (sirt6) level and clinicopathological characteristics and prognosis of gastric cancer (GC) patients. METHODS: The serum sirt6 levels of subjects (135 cases of GC, 68 cases of atrophic gastritis, 60 cases of healthy controls) were analyzed...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704893/ https://www.ncbi.nlm.nih.gov/pubmed/36451443 http://dx.doi.org/10.1097/MD.0000000000031568 |
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author | Li, Danyang Cao, Cheng |
author_facet | Li, Danyang Cao, Cheng |
author_sort | Li, Danyang |
collection | PubMed |
description | We aimed to evaluate the correlation between serum sirtuin 6 (sirt6) level and clinicopathological characteristics and prognosis of gastric cancer (GC) patients. METHODS: The serum sirt6 levels of subjects (135 cases of GC, 68 cases of atrophic gastritis, 60 cases of healthy controls) were analyzed by enzyme-linked immunosorbent assay. The predictive and prognostic values of sirt6 serum level for GC were determined by performing receiver operating characteristic curve (ROC), Kaplan–Meier analysis, as well as univariate and multivariate Cox regression, respectively. RESULTS: GC patients showed lower sirt6 serum levels than that of atrophic gastritis patients and healthy control. Taking the healthy control as a reference, the area under the ROC curve (AUC) of sirt6 serum level for diagnosing GC was 0.955 with a sensitivity of 91.85% and a specificity of 90.0%. Based on ROC analysis using atrophic gastritis as the state variable, serum sirt6 had a high diagnostic efficiency for GC (AUC = 0.754). Serum sirt6 was related to the clinicopathological features (tumor size, Lauren’s classification, tumor node metastasis staging, lymph node metastasis) and overall survival (log-rank χ(2) = 12.22, P < .001). The AUC of serum sirt6 predicting death in GC patients was 0.731. At the optimal cutoff value (16.83 ng/mL), the sensitivity and specificity of sirt6 were 59.57% and 79.55%, respectively. Moreover, lower sirt6 level as independent risk factor was revealed to affect prognosis of GC patients (P = .018). CONCLUSION: Serum sirt6 level was positively associated with the tumor stage and metastasis conditions, which could be served as diagnostic and predictive biomarkers in GC. |
format | Online Article Text |
id | pubmed-9704893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-97048932022-11-29 The correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer Li, Danyang Cao, Cheng Medicine (Baltimore) 4500 We aimed to evaluate the correlation between serum sirtuin 6 (sirt6) level and clinicopathological characteristics and prognosis of gastric cancer (GC) patients. METHODS: The serum sirt6 levels of subjects (135 cases of GC, 68 cases of atrophic gastritis, 60 cases of healthy controls) were analyzed by enzyme-linked immunosorbent assay. The predictive and prognostic values of sirt6 serum level for GC were determined by performing receiver operating characteristic curve (ROC), Kaplan–Meier analysis, as well as univariate and multivariate Cox regression, respectively. RESULTS: GC patients showed lower sirt6 serum levels than that of atrophic gastritis patients and healthy control. Taking the healthy control as a reference, the area under the ROC curve (AUC) of sirt6 serum level for diagnosing GC was 0.955 with a sensitivity of 91.85% and a specificity of 90.0%. Based on ROC analysis using atrophic gastritis as the state variable, serum sirt6 had a high diagnostic efficiency for GC (AUC = 0.754). Serum sirt6 was related to the clinicopathological features (tumor size, Lauren’s classification, tumor node metastasis staging, lymph node metastasis) and overall survival (log-rank χ(2) = 12.22, P < .001). The AUC of serum sirt6 predicting death in GC patients was 0.731. At the optimal cutoff value (16.83 ng/mL), the sensitivity and specificity of sirt6 were 59.57% and 79.55%, respectively. Moreover, lower sirt6 level as independent risk factor was revealed to affect prognosis of GC patients (P = .018). CONCLUSION: Serum sirt6 level was positively associated with the tumor stage and metastasis conditions, which could be served as diagnostic and predictive biomarkers in GC. Lippincott Williams & Wilkins 2022-11-25 /pmc/articles/PMC9704893/ /pubmed/36451443 http://dx.doi.org/10.1097/MD.0000000000031568 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | 4500 Li, Danyang Cao, Cheng The correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer |
title | The correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer |
title_full | The correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer |
title_fullStr | The correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer |
title_full_unstemmed | The correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer |
title_short | The correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer |
title_sort | correlation of serum sirt6 with clinical outcome and prognosis in patients with gastric cancer |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704893/ https://www.ncbi.nlm.nih.gov/pubmed/36451443 http://dx.doi.org/10.1097/MD.0000000000031568 |
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