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Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysis

Background: With the increasing number of new cancer cases and mortality rates, cancer has become a serious global health problem, but there are no ideal cancer biomarkers for effective diagnosis. Currently, mounting evidence demonstrates that lncRNAs play a fundamental role in cancer progression. B...

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Autores principales: Lin, Guangyao, Wang, Yongzhou, Deng, Li, Ye, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453800/
https://www.ncbi.nlm.nih.gov/pubmed/37636267
http://dx.doi.org/10.3389/fgene.2023.1234040
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author Lin, Guangyao
Wang, Yongzhou
Deng, Li
Ye, Tao
author_facet Lin, Guangyao
Wang, Yongzhou
Deng, Li
Ye, Tao
author_sort Lin, Guangyao
collection PubMed
description Background: With the increasing number of new cancer cases and mortality rates, cancer has become a serious global health problem, but there are no ideal cancer biomarkers for effective diagnosis. Currently, mounting evidence demonstrates that lncRNAs play a fundamental role in cancer progression. BBOX1 anti-sense RNA 1 (BBOX1-AS1) is a recently clarified lncRNA and has been identified as dysregulated in various carcinomas, and it contributes to poor survival in cancer patients. Methods: We thoroughly searched six databases for eligible articles published as of 27, April 2023. The association of BBOX1-AS1 expression levels with prognostic and clinicopathological parameters was assessed by odds ratios (OR) and hazard ratios with 95% CIs. Additionally, we further validated our results utilizing the GEPIA online database. Results: Eight studies comprising 602 patients were included in this analysis. High BBOX1-AS1 expression indicated poor overall survival (OS) (hazard ratios = 2.30, 95% Cl [1.99, 2.67], p < 0.00001) when compared with low BBOX1-AS1 expression. Furthermore, BBOX1-AS1 expression was positively correlated with lymph node metastasis (OR = 3.00, 95% CI [1.71–5.28], p = 0.0001) and advanced tumor stage (OR = 3.74, 95% CI [2.63–5.32], p < 0.00001) for cancer patients. Moreover, BBOX1-AS1 was remarkably upregulated in 12 malignancies, and the elevated BBOX1-AS1 expression predicted poorer OS and worse disease-free survival (DFS) confirmed through the GEPIA online gene analysis tool. Conclusion: The findings highlight that BBOX1-AS1 was significantly associated with detrimental overall survival, disease-free survival, lymph node metastasis and tumor stage; thus, it could act as a novel promising biomarker to predict the clinicopathological characteristics and prognosis for various cancers.
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spelling pubmed-104538002023-08-26 Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysis Lin, Guangyao Wang, Yongzhou Deng, Li Ye, Tao Front Genet Genetics Background: With the increasing number of new cancer cases and mortality rates, cancer has become a serious global health problem, but there are no ideal cancer biomarkers for effective diagnosis. Currently, mounting evidence demonstrates that lncRNAs play a fundamental role in cancer progression. BBOX1 anti-sense RNA 1 (BBOX1-AS1) is a recently clarified lncRNA and has been identified as dysregulated in various carcinomas, and it contributes to poor survival in cancer patients. Methods: We thoroughly searched six databases for eligible articles published as of 27, April 2023. The association of BBOX1-AS1 expression levels with prognostic and clinicopathological parameters was assessed by odds ratios (OR) and hazard ratios with 95% CIs. Additionally, we further validated our results utilizing the GEPIA online database. Results: Eight studies comprising 602 patients were included in this analysis. High BBOX1-AS1 expression indicated poor overall survival (OS) (hazard ratios = 2.30, 95% Cl [1.99, 2.67], p < 0.00001) when compared with low BBOX1-AS1 expression. Furthermore, BBOX1-AS1 expression was positively correlated with lymph node metastasis (OR = 3.00, 95% CI [1.71–5.28], p = 0.0001) and advanced tumor stage (OR = 3.74, 95% CI [2.63–5.32], p < 0.00001) for cancer patients. Moreover, BBOX1-AS1 was remarkably upregulated in 12 malignancies, and the elevated BBOX1-AS1 expression predicted poorer OS and worse disease-free survival (DFS) confirmed through the GEPIA online gene analysis tool. Conclusion: The findings highlight that BBOX1-AS1 was significantly associated with detrimental overall survival, disease-free survival, lymph node metastasis and tumor stage; thus, it could act as a novel promising biomarker to predict the clinicopathological characteristics and prognosis for various cancers. Frontiers Media S.A. 2023-08-11 /pmc/articles/PMC10453800/ /pubmed/37636267 http://dx.doi.org/10.3389/fgene.2023.1234040 Text en Copyright © 2023 Lin, Wang, Deng and Ye. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Lin, Guangyao
Wang, Yongzhou
Deng, Li
Ye, Tao
Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysis
title Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysis
title_full Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysis
title_fullStr Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysis
title_full_unstemmed Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysis
title_short Prognostic effect of lncRNA BBOX1-AS1 in malignancies: a meta-analysis
title_sort prognostic effect of lncrna bbox1-as1 in malignancies: a meta-analysis
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453800/
https://www.ncbi.nlm.nih.gov/pubmed/37636267
http://dx.doi.org/10.3389/fgene.2023.1234040
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