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Prognostic and clinicopathological value of circPVT1 in human cancers: A meta‐analysis
BACKGROUND: Circular RNA PVT1 (circPVT1) is significantly upregulated in various human cancers and is related to poor clinical outcome of cancer patients. However, the prognostic and clinicopathological value of circPVT1 in diverse human cancers remains controversial and inconclusive. AIM: The objec...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551984/ https://www.ncbi.nlm.nih.gov/pubmed/33793089 http://dx.doi.org/10.1002/cnr2.1385 |
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author | Lin, Zhengjun Tang, Xianzhe Wang, Lu Ling, Lin |
author_facet | Lin, Zhengjun Tang, Xianzhe Wang, Lu Ling, Lin |
author_sort | Lin, Zhengjun |
collection | PubMed |
description | BACKGROUND: Circular RNA PVT1 (circPVT1) is significantly upregulated in various human cancers and is related to poor clinical outcome of cancer patients. However, the prognostic and clinicopathological value of circPVT1 in diverse human cancers remains controversial and inconclusive. AIM: The objective of our study is to evaluate the prognostic and clinicopathological role of circPVT1 for cancer patients. METHODS AND RESULTS: PubMed, Embase, Web of Science, and Cochrane Library were searched for eligible studies by October 1, 2020. The correlation between circPVT1 expression, and overall survival (OS) and clinical parameters was assessed by pooled hazard ratios (HRs) and odds ratios (ORs) with 95% confidence intervals (CIs). Subgroup analyses, heterogeneity, and publication bias were conducted to further enhance reliability. Twelve studies (1282 patients) were selected for this meta‐analysis, including 11 on prognosis and 10 on clinicopathological parameters. Elevated expression of circPVT1 was associated with a worse OS in cancer patients (HR, 2.009; 95% CI, 1.667‐2.408, 1.892; P < .001). For clinicopathological value, upregulation of circPVT1 was closely related to poor clinical parameters lymph node metastasis (OR = 2.019; 95% CI, 1.026‐3.976; P = .042; I (2) = 77.5%; P(H) = 0.000), late clinical stage (OR = 3.594; 95% CI, 1.828‐7.065; P < .001; I (2) = 71.7%; P(H) = 0.001), distant metastasis (OR = 4.598; 95% CI, 1.411‐14.988; P = .011; I (2) = 78.1%; P(H) = 0.001), and chemoresistant (OR = 6.400; 95% CI, 2.107‐19.441; P = .001; I (2) = 49.6%; P(H) = 0.159). CONCLUSION: High expression of circPVT1 is correlated with unfavorable prognosis of cancer patients, indicating that circPVT1 can function as a potential prognostic biomarker in human cancer. |
format | Online Article Text |
id | pubmed-8551984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85519842021-11-04 Prognostic and clinicopathological value of circPVT1 in human cancers: A meta‐analysis Lin, Zhengjun Tang, Xianzhe Wang, Lu Ling, Lin Cancer Rep (Hoboken) Original Articles BACKGROUND: Circular RNA PVT1 (circPVT1) is significantly upregulated in various human cancers and is related to poor clinical outcome of cancer patients. However, the prognostic and clinicopathological value of circPVT1 in diverse human cancers remains controversial and inconclusive. AIM: The objective of our study is to evaluate the prognostic and clinicopathological role of circPVT1 for cancer patients. METHODS AND RESULTS: PubMed, Embase, Web of Science, and Cochrane Library were searched for eligible studies by October 1, 2020. The correlation between circPVT1 expression, and overall survival (OS) and clinical parameters was assessed by pooled hazard ratios (HRs) and odds ratios (ORs) with 95% confidence intervals (CIs). Subgroup analyses, heterogeneity, and publication bias were conducted to further enhance reliability. Twelve studies (1282 patients) were selected for this meta‐analysis, including 11 on prognosis and 10 on clinicopathological parameters. Elevated expression of circPVT1 was associated with a worse OS in cancer patients (HR, 2.009; 95% CI, 1.667‐2.408, 1.892; P < .001). For clinicopathological value, upregulation of circPVT1 was closely related to poor clinical parameters lymph node metastasis (OR = 2.019; 95% CI, 1.026‐3.976; P = .042; I (2) = 77.5%; P(H) = 0.000), late clinical stage (OR = 3.594; 95% CI, 1.828‐7.065; P < .001; I (2) = 71.7%; P(H) = 0.001), distant metastasis (OR = 4.598; 95% CI, 1.411‐14.988; P = .011; I (2) = 78.1%; P(H) = 0.001), and chemoresistant (OR = 6.400; 95% CI, 2.107‐19.441; P = .001; I (2) = 49.6%; P(H) = 0.159). CONCLUSION: High expression of circPVT1 is correlated with unfavorable prognosis of cancer patients, indicating that circPVT1 can function as a potential prognostic biomarker in human cancer. John Wiley and Sons Inc. 2021-04-01 /pmc/articles/PMC8551984/ /pubmed/33793089 http://dx.doi.org/10.1002/cnr2.1385 Text en © 2021 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Lin, Zhengjun Tang, Xianzhe Wang, Lu Ling, Lin Prognostic and clinicopathological value of circPVT1 in human cancers: A meta‐analysis |
title | Prognostic and clinicopathological value of circPVT1 in human cancers: A meta‐analysis |
title_full | Prognostic and clinicopathological value of circPVT1 in human cancers: A meta‐analysis |
title_fullStr | Prognostic and clinicopathological value of circPVT1 in human cancers: A meta‐analysis |
title_full_unstemmed | Prognostic and clinicopathological value of circPVT1 in human cancers: A meta‐analysis |
title_short | Prognostic and clinicopathological value of circPVT1 in human cancers: A meta‐analysis |
title_sort | prognostic and clinicopathological value of circpvt1 in human cancers: a meta‐analysis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551984/ https://www.ncbi.nlm.nih.gov/pubmed/33793089 http://dx.doi.org/10.1002/cnr2.1385 |
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