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Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis

Background: We conducted this research to investigate the relationship between long intergenic non-protein coding RNA 673 (linc00673) expression and prognosis and clinicopathological parameters in human malignancies. Methods: The PubMed, Embase, WOS, and CNKI databases were used to collect eligible...

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Autores principales: Zhu, Yurong, Zhang, Zhifa, Peng, Hui, Li, Weiping, Hu, Shaowei, Zhao, Min, Lin, Weifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319490/
https://www.ncbi.nlm.nih.gov/pubmed/34231850
http://dx.doi.org/10.1042/BSR20211175
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author Zhu, Yurong
Zhang, Zhifa
Peng, Hui
Li, Weiping
Hu, Shaowei
Zhao, Min
Lin, Weifeng
author_facet Zhu, Yurong
Zhang, Zhifa
Peng, Hui
Li, Weiping
Hu, Shaowei
Zhao, Min
Lin, Weifeng
author_sort Zhu, Yurong
collection PubMed
description Background: We conducted this research to investigate the relationship between long intergenic non-protein coding RNA 673 (linc00673) expression and prognosis and clinicopathological parameters in human malignancies. Methods: The PubMed, Embase, WOS, and CNKI databases were used to collect eligible research data before 4 January 2021. Meta-analysis was performed using Stata 12.0 software. Pooled odds ratios (ORs) or hazard ratios (HRs) and their 95% confidence interval (CIs) were calculated to evaluate the association of linc00673 expression with survival outcomes and clinical parameters. Results: We finally included 17 articles and a total of 1539 cases for the meta-analysis. The results indicated that linc00673 was significantly correlated with T stage (P=0.006), tumor stage (P<0.001), lymph node metastasis (P<0.001), and distant metastasis (P<0.001). In addition, the results suggested that elevated linc00673 expression predicted a poor overall survival (OS) time (P=0.013) and acted as an independent prognostic factor (P<0.001) for OS in patients with malignancy. Although potential evidence of publication bias was found in the studies on OS in relation to tumor stage in the multivariate analysis, the trim-and-fill analysis confirmed that the results remained stable. Conclusions: Overexpression of linc00673 was significantly correlated with shorter OS time in patients with malignant tumors. Moreover, the increased expression level of linc00673 was significantly correlated with T stage, tumor stage, lymph node metastasis, and distant metastasis. The results presented in this article revealed that linc00673 might be involved in the progression and invasion of malignancy and serve as a novel prognostic biomarker and potential therapeutic target for malignancy.
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spelling pubmed-83194902021-08-10 Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis Zhu, Yurong Zhang, Zhifa Peng, Hui Li, Weiping Hu, Shaowei Zhao, Min Lin, Weifeng Biosci Rep Neuroscience Background: We conducted this research to investigate the relationship between long intergenic non-protein coding RNA 673 (linc00673) expression and prognosis and clinicopathological parameters in human malignancies. Methods: The PubMed, Embase, WOS, and CNKI databases were used to collect eligible research data before 4 January 2021. Meta-analysis was performed using Stata 12.0 software. Pooled odds ratios (ORs) or hazard ratios (HRs) and their 95% confidence interval (CIs) were calculated to evaluate the association of linc00673 expression with survival outcomes and clinical parameters. Results: We finally included 17 articles and a total of 1539 cases for the meta-analysis. The results indicated that linc00673 was significantly correlated with T stage (P=0.006), tumor stage (P<0.001), lymph node metastasis (P<0.001), and distant metastasis (P<0.001). In addition, the results suggested that elevated linc00673 expression predicted a poor overall survival (OS) time (P=0.013) and acted as an independent prognostic factor (P<0.001) for OS in patients with malignancy. Although potential evidence of publication bias was found in the studies on OS in relation to tumor stage in the multivariate analysis, the trim-and-fill analysis confirmed that the results remained stable. Conclusions: Overexpression of linc00673 was significantly correlated with shorter OS time in patients with malignant tumors. Moreover, the increased expression level of linc00673 was significantly correlated with T stage, tumor stage, lymph node metastasis, and distant metastasis. The results presented in this article revealed that linc00673 might be involved in the progression and invasion of malignancy and serve as a novel prognostic biomarker and potential therapeutic target for malignancy. Portland Press Ltd. 2021-07-28 /pmc/articles/PMC8319490/ /pubmed/34231850 http://dx.doi.org/10.1042/BSR20211175 Text en © 2021 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Neuroscience
Zhu, Yurong
Zhang, Zhifa
Peng, Hui
Li, Weiping
Hu, Shaowei
Zhao, Min
Lin, Weifeng
Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis
title Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis
title_full Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis
title_fullStr Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis
title_full_unstemmed Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis
title_short Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis
title_sort clinicopathological and prognostic significance of linc00673 in human malignancy: a review and meta-analysis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319490/
https://www.ncbi.nlm.nih.gov/pubmed/34231850
http://dx.doi.org/10.1042/BSR20211175
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