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Expression of the HOXA gene family and its relationship to prognosis and immune infiltrates in cervical cancer

BACKGROUND: The homeobox A cluster (HOXA) gene family is participated in multiple biological functions in human cancers. To date, little is known about the expression profile and clinical significance of HOXA genes in cervical cancer. METHODS: We downloaded RNASeq data of cervical cancer from The Ca...

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Autores principales: Ge, Fenfen, Tie, Weiwei, Zhang, Junli, Zhu, Yingying, Fan, Yingying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605136/
https://www.ncbi.nlm.nih.gov/pubmed/34606634
http://dx.doi.org/10.1002/jcla.24015
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author Ge, Fenfen
Tie, Weiwei
Zhang, Junli
Zhu, Yingying
Fan, Yingying
author_facet Ge, Fenfen
Tie, Weiwei
Zhang, Junli
Zhu, Yingying
Fan, Yingying
author_sort Ge, Fenfen
collection PubMed
description BACKGROUND: The homeobox A cluster (HOXA) gene family is participated in multiple biological functions in human cancers. To date, little is known about the expression profile and clinical significance of HOXA genes in cervical cancer. METHODS: We downloaded RNASeq data of cervical cancer from The Cancer Genome Atlas (TCGA) database. The difference in HOXA family expression was analyzed using independent samples t test. Cox proportional hazard regression analysis was used to assess the effect of HOXA family expression on survival, and a nomogram predicting survival was generated. We assessed the infiltration difference in immune cells and expression difference of immunity biomarkers between two groups with different expression level of HOXA genes through Immune Cell Abundance Identifier (ImmuCellAI) and independent samples t test, respectively. RESULTS: Our results showed that the HOXA1 gene was upregulated, while the HOXA10 and HOXA11 were downregulated in cervical cancer. Downregulation of HOXA1 was related to a poor outcome for cervical cancer patient. We also identified a significantly increased abundance of T helper 2 cells (Th2) and higher expression of PD‐L1 in cervical cancer patients with lower expression of HOXA10 and HOXA11. The gene set enrichment analysis (GSEA) results indicated that HOXA1 and HOXA11 were involved in immune responses pathways and participated in the activation of a variety of classic signaling pathways related to the progression of human cancer. CONCLUSION: This study comprehensively analyzed different HOXA genes applying public database to determine their expression patterns, potential diagnostic, prognostic, and treatment values in cervical cancer.
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spelling pubmed-86051362021-11-24 Expression of the HOXA gene family and its relationship to prognosis and immune infiltrates in cervical cancer Ge, Fenfen Tie, Weiwei Zhang, Junli Zhu, Yingying Fan, Yingying J Clin Lab Anal Research Articles BACKGROUND: The homeobox A cluster (HOXA) gene family is participated in multiple biological functions in human cancers. To date, little is known about the expression profile and clinical significance of HOXA genes in cervical cancer. METHODS: We downloaded RNASeq data of cervical cancer from The Cancer Genome Atlas (TCGA) database. The difference in HOXA family expression was analyzed using independent samples t test. Cox proportional hazard regression analysis was used to assess the effect of HOXA family expression on survival, and a nomogram predicting survival was generated. We assessed the infiltration difference in immune cells and expression difference of immunity biomarkers between two groups with different expression level of HOXA genes through Immune Cell Abundance Identifier (ImmuCellAI) and independent samples t test, respectively. RESULTS: Our results showed that the HOXA1 gene was upregulated, while the HOXA10 and HOXA11 were downregulated in cervical cancer. Downregulation of HOXA1 was related to a poor outcome for cervical cancer patient. We also identified a significantly increased abundance of T helper 2 cells (Th2) and higher expression of PD‐L1 in cervical cancer patients with lower expression of HOXA10 and HOXA11. The gene set enrichment analysis (GSEA) results indicated that HOXA1 and HOXA11 were involved in immune responses pathways and participated in the activation of a variety of classic signaling pathways related to the progression of human cancer. CONCLUSION: This study comprehensively analyzed different HOXA genes applying public database to determine their expression patterns, potential diagnostic, prognostic, and treatment values in cervical cancer. John Wiley and Sons Inc. 2021-10-04 /pmc/articles/PMC8605136/ /pubmed/34606634 http://dx.doi.org/10.1002/jcla.24015 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis 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 Research Articles
Ge, Fenfen
Tie, Weiwei
Zhang, Junli
Zhu, Yingying
Fan, Yingying
Expression of the HOXA gene family and its relationship to prognosis and immune infiltrates in cervical cancer
title Expression of the HOXA gene family and its relationship to prognosis and immune infiltrates in cervical cancer
title_full Expression of the HOXA gene family and its relationship to prognosis and immune infiltrates in cervical cancer
title_fullStr Expression of the HOXA gene family and its relationship to prognosis and immune infiltrates in cervical cancer
title_full_unstemmed Expression of the HOXA gene family and its relationship to prognosis and immune infiltrates in cervical cancer
title_short Expression of the HOXA gene family and its relationship to prognosis and immune infiltrates in cervical cancer
title_sort expression of the hoxa gene family and its relationship to prognosis and immune infiltrates in cervical cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605136/
https://www.ncbi.nlm.nih.gov/pubmed/34606634
http://dx.doi.org/10.1002/jcla.24015
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