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CMTM6 as a candidate risk gene for cervical cancer: Comprehensive bioinformatics study

Background: CKLF like MARVEL transmembrane domain containing 6 (CMTM6) is an important programmed cell death 1 ligand 1 regulator (PD-L1). CMTM6 was reported as an important regulator of PD-L1 by promoting PD-L1 expression in tumor cells against T cells. However, the function of CMTM6 in cervical ca...

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Autores principales: Huang, Xiaoting, Liu, Wei, Liu, Chunshan, Hu, Jijie, Wang, Baiyao, Ren, Anbang, Huang, Xiaona, Yuan, Yawei, Liu, Jinquan, Li, Mingyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798917/
https://www.ncbi.nlm.nih.gov/pubmed/36589225
http://dx.doi.org/10.3389/fmolb.2022.983410
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author Huang, Xiaoting
Liu, Wei
Liu, Chunshan
Hu, Jijie
Wang, Baiyao
Ren, Anbang
Huang, Xiaona
Yuan, Yawei
Liu, Jinquan
Li, Mingyi
author_facet Huang, Xiaoting
Liu, Wei
Liu, Chunshan
Hu, Jijie
Wang, Baiyao
Ren, Anbang
Huang, Xiaona
Yuan, Yawei
Liu, Jinquan
Li, Mingyi
author_sort Huang, Xiaoting
collection PubMed
description Background: CKLF like MARVEL transmembrane domain containing 6 (CMTM6) is an important programmed cell death 1 ligand 1 regulator (PD-L1). CMTM6 was reported as an important regulator of PD-L1 by promoting PD-L1 expression in tumor cells against T cells. However, the function of CMTM6 in cervical cancer is not well characterized. In addition, the role of CMTM6 in the induction of epithelial-mesenchymal transition (EMT) in the context of cervical cancer is unknown. Methods: In this study, we evaluated the role of CMTM6, including gene expression analysis, miRNA target regulation, and methylation characteristic, using multiple bioinformatics tools based on The Cancer Genome Atlas (TCGA) database. The expression of CMTM6 in cervical cancer tissues and non-cancerous adjacent tissues was assessed using immunohistochemistry. In vitro and in vivo function experiments were performed to explore the effects of CMTM6 on growth and metastasis of cervical cancer. Results: Human cervical cancer tissues showed higher expression of CMTM6 than the adjacent non-cancerous tissues. In vitro assays showed that CMTM6 promoted cervical cancer cell invasion, migration, proliferation, and epithelial-mesenchymal transition via activation of mitogen-activated protein kinase (MAPK) c-jun N-terminal kinase (JNK)/p38 signaling pathway. We identified transcription factors (TFs), miRNAs, and immune cells that may interact with CMTM6. Conclusion: These results indicate that CMTM6 is a potential therapeutic target in the context of cervical cancer.
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spelling pubmed-97989172022-12-30 CMTM6 as a candidate risk gene for cervical cancer: Comprehensive bioinformatics study Huang, Xiaoting Liu, Wei Liu, Chunshan Hu, Jijie Wang, Baiyao Ren, Anbang Huang, Xiaona Yuan, Yawei Liu, Jinquan Li, Mingyi Front Mol Biosci Molecular Biosciences Background: CKLF like MARVEL transmembrane domain containing 6 (CMTM6) is an important programmed cell death 1 ligand 1 regulator (PD-L1). CMTM6 was reported as an important regulator of PD-L1 by promoting PD-L1 expression in tumor cells against T cells. However, the function of CMTM6 in cervical cancer is not well characterized. In addition, the role of CMTM6 in the induction of epithelial-mesenchymal transition (EMT) in the context of cervical cancer is unknown. Methods: In this study, we evaluated the role of CMTM6, including gene expression analysis, miRNA target regulation, and methylation characteristic, using multiple bioinformatics tools based on The Cancer Genome Atlas (TCGA) database. The expression of CMTM6 in cervical cancer tissues and non-cancerous adjacent tissues was assessed using immunohistochemistry. In vitro and in vivo function experiments were performed to explore the effects of CMTM6 on growth and metastasis of cervical cancer. Results: Human cervical cancer tissues showed higher expression of CMTM6 than the adjacent non-cancerous tissues. In vitro assays showed that CMTM6 promoted cervical cancer cell invasion, migration, proliferation, and epithelial-mesenchymal transition via activation of mitogen-activated protein kinase (MAPK) c-jun N-terminal kinase (JNK)/p38 signaling pathway. We identified transcription factors (TFs), miRNAs, and immune cells that may interact with CMTM6. Conclusion: These results indicate that CMTM6 is a potential therapeutic target in the context of cervical cancer. Frontiers Media S.A. 2022-12-12 /pmc/articles/PMC9798917/ /pubmed/36589225 http://dx.doi.org/10.3389/fmolb.2022.983410 Text en Copyright © 2022 Huang, Liu, Liu, Hu, Wang, Ren, Huang, Yuan, Liu and Li. 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 Molecular Biosciences
Huang, Xiaoting
Liu, Wei
Liu, Chunshan
Hu, Jijie
Wang, Baiyao
Ren, Anbang
Huang, Xiaona
Yuan, Yawei
Liu, Jinquan
Li, Mingyi
CMTM6 as a candidate risk gene for cervical cancer: Comprehensive bioinformatics study
title CMTM6 as a candidate risk gene for cervical cancer: Comprehensive bioinformatics study
title_full CMTM6 as a candidate risk gene for cervical cancer: Comprehensive bioinformatics study
title_fullStr CMTM6 as a candidate risk gene for cervical cancer: Comprehensive bioinformatics study
title_full_unstemmed CMTM6 as a candidate risk gene for cervical cancer: Comprehensive bioinformatics study
title_short CMTM6 as a candidate risk gene for cervical cancer: Comprehensive bioinformatics study
title_sort cmtm6 as a candidate risk gene for cervical cancer: comprehensive bioinformatics study
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798917/
https://www.ncbi.nlm.nih.gov/pubmed/36589225
http://dx.doi.org/10.3389/fmolb.2022.983410
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