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The clinical prognostic value of long noncoding RNA HAND2-AS1 in cancer patients: A study based on meta-analysis and TCGA data (PRISMA)

The heart and neural crest derivatives expressed 2 antisense RNA 1 (HAND2-AS1) is a novel long noncoding RNA aberrantly expressed in human malignancies. We aimed to analyze the available data to evaluate the clinical prognostic significance of HAND2-AS1 in tumors. METHODS: In this meta-analysis, ele...

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Autores principales: Yan, Zhaoyang, Lu, Juntao, Xu, Xinjian, You, Yang, Xu, Jinsheng, Xu, Tongxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524981/
https://www.ncbi.nlm.nih.gov/pubmed/36181101
http://dx.doi.org/10.1097/MD.0000000000030789
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author Yan, Zhaoyang
Lu, Juntao
Xu, Xinjian
You, Yang
Xu, Jinsheng
Xu, Tongxin
author_facet Yan, Zhaoyang
Lu, Juntao
Xu, Xinjian
You, Yang
Xu, Jinsheng
Xu, Tongxin
author_sort Yan, Zhaoyang
collection PubMed
description The heart and neural crest derivatives expressed 2 antisense RNA 1 (HAND2-AS1) is a novel long noncoding RNA aberrantly expressed in human malignancies. We aimed to analyze the available data to evaluate the clinical prognostic significance of HAND2-AS1 in tumors. METHODS: In this meta-analysis, electronic databases, including PubMed Cochrane Library, EMBASE, Medline, Web of Science, CNKI, and Wanfang, were searched from their inception up to December 1, 2021. The pooled hazard ratios (HRs) or odds ratios (ORs) with 95% confidence intervals (95% CIs) were calculated to assess the relationship of HAND2-AS1expression level with prognosis and clinicopathological features in cancer patients. The publication bias was identified by Begg’s test, and the sensitivity analysis was also performed. RESULTS: A total of 10 articles with 615 patients were included in the present meta-analysis. The combined results revealed that low expression of HAND2-AS1 was associated with poor overall survival (OS) (HR = 0.48, 95% CI: 0.36–0.64, P < .001) in a variety of cancers. In addition, the decrease in HAND2-AS1 expression was also correlated with poor differentiation (OR = 4.36, 95% CI: 2.15–8.87, P < .001) and lymph node metastasis (OR = 0.26, 95% CI: 0.13–0.54, P < .001). The cancer genome atlas (TCGA) dataset further demonstrated that low expression of HAND2-AS1 was associated with poor OS and disease-free survival. CONCLUSIONS: Our results of this meta-analysis indicated that HAND2-AS1 may be a prognostic marker and even a therapeutic target for human cancer.
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spelling pubmed-95249812022-10-03 The clinical prognostic value of long noncoding RNA HAND2-AS1 in cancer patients: A study based on meta-analysis and TCGA data (PRISMA) Yan, Zhaoyang Lu, Juntao Xu, Xinjian You, Yang Xu, Jinsheng Xu, Tongxin Medicine (Baltimore) Research Article The heart and neural crest derivatives expressed 2 antisense RNA 1 (HAND2-AS1) is a novel long noncoding RNA aberrantly expressed in human malignancies. We aimed to analyze the available data to evaluate the clinical prognostic significance of HAND2-AS1 in tumors. METHODS: In this meta-analysis, electronic databases, including PubMed Cochrane Library, EMBASE, Medline, Web of Science, CNKI, and Wanfang, were searched from their inception up to December 1, 2021. The pooled hazard ratios (HRs) or odds ratios (ORs) with 95% confidence intervals (95% CIs) were calculated to assess the relationship of HAND2-AS1expression level with prognosis and clinicopathological features in cancer patients. The publication bias was identified by Begg’s test, and the sensitivity analysis was also performed. RESULTS: A total of 10 articles with 615 patients were included in the present meta-analysis. The combined results revealed that low expression of HAND2-AS1 was associated with poor overall survival (OS) (HR = 0.48, 95% CI: 0.36–0.64, P < .001) in a variety of cancers. In addition, the decrease in HAND2-AS1 expression was also correlated with poor differentiation (OR = 4.36, 95% CI: 2.15–8.87, P < .001) and lymph node metastasis (OR = 0.26, 95% CI: 0.13–0.54, P < .001). The cancer genome atlas (TCGA) dataset further demonstrated that low expression of HAND2-AS1 was associated with poor OS and disease-free survival. CONCLUSIONS: Our results of this meta-analysis indicated that HAND2-AS1 may be a prognostic marker and even a therapeutic target for human cancer. Lippincott Williams & Wilkins 2022-09-30 /pmc/articles/PMC9524981/ /pubmed/36181101 http://dx.doi.org/10.1097/MD.0000000000030789 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yan, Zhaoyang
Lu, Juntao
Xu, Xinjian
You, Yang
Xu, Jinsheng
Xu, Tongxin
The clinical prognostic value of long noncoding RNA HAND2-AS1 in cancer patients: A study based on meta-analysis and TCGA data (PRISMA)
title The clinical prognostic value of long noncoding RNA HAND2-AS1 in cancer patients: A study based on meta-analysis and TCGA data (PRISMA)
title_full The clinical prognostic value of long noncoding RNA HAND2-AS1 in cancer patients: A study based on meta-analysis and TCGA data (PRISMA)
title_fullStr The clinical prognostic value of long noncoding RNA HAND2-AS1 in cancer patients: A study based on meta-analysis and TCGA data (PRISMA)
title_full_unstemmed The clinical prognostic value of long noncoding RNA HAND2-AS1 in cancer patients: A study based on meta-analysis and TCGA data (PRISMA)
title_short The clinical prognostic value of long noncoding RNA HAND2-AS1 in cancer patients: A study based on meta-analysis and TCGA data (PRISMA)
title_sort clinical prognostic value of long noncoding rna hand2-as1 in cancer patients: a study based on meta-analysis and tcga data (prisma)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524981/
https://www.ncbi.nlm.nih.gov/pubmed/36181101
http://dx.doi.org/10.1097/MD.0000000000030789
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