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CMTM3 as a Potential New Immune Checkpoint Regulator
OBJECTIVES: To evaluate the role of CKLF-like MARVEL transmembrane domain containing 3 (CMTM3) in tumor microenvironment and cancer immunotherapy and explore its potential mechanism. METHOD: The cancer genome map was obtained from the UCSC Xena database. RNAseq data from the Genotype-Tissue Expressi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553517/ https://www.ncbi.nlm.nih.gov/pubmed/36245970 http://dx.doi.org/10.1155/2022/2103515 |
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author | Shen, Qian Cong, Zhirong Zhou, Ying Teng, Yue Gao, Jin Tang, Weiyan |
author_facet | Shen, Qian Cong, Zhirong Zhou, Ying Teng, Yue Gao, Jin Tang, Weiyan |
author_sort | Shen, Qian |
collection | PubMed |
description | OBJECTIVES: To evaluate the role of CKLF-like MARVEL transmembrane domain containing 3 (CMTM3) in tumor microenvironment and cancer immunotherapy and explore its potential mechanism. METHOD: The cancer genome map was obtained from the UCSC Xena database. RNAseq data from the Genotype-Tissue Expression (GTEx) and The Cancer Genome Atlas (TCGA) databases were utilized for evaluating the expression and prognostic value of CMTM3 through survival data of clinical trials. The enrichment analysis of CMTM3 was performed using the R package “clusterProfiler.” The scores of immune cell infiltration in TCGA samples were downloaded from the ImmuCellAI database and TIMER2 database, and the relationship between both immune cell invasion and CMTM3 expression was investigated. Immunological activation and suppression genes, immune checkpoints, chemokines, and their receptors were all investigated in relation to CMTM3. RESULTS: Most tumor types had varied levels of CMTM3 expression and predicted poor survival status. The CMTM3 expression is closely associated with cancer-associated fibroblasts, macrophages, myeloid dendritic cells, endothelial cells, immune activation genes, immune suppressor genes, immune checkpoints, chemokines, and related receptors. CONCLUSION: Our data reveal that CMTM3 might be used as a cancer biomarker. CMTM3 may work in conjunction with other immunological checkpoints to alter the immune milieu, which could lead to the establishment of new immunotherapy medicines. |
format | Online Article Text |
id | pubmed-9553517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-95535172022-10-13 CMTM3 as a Potential New Immune Checkpoint Regulator Shen, Qian Cong, Zhirong Zhou, Ying Teng, Yue Gao, Jin Tang, Weiyan J Oncol Research Article OBJECTIVES: To evaluate the role of CKLF-like MARVEL transmembrane domain containing 3 (CMTM3) in tumor microenvironment and cancer immunotherapy and explore its potential mechanism. METHOD: The cancer genome map was obtained from the UCSC Xena database. RNAseq data from the Genotype-Tissue Expression (GTEx) and The Cancer Genome Atlas (TCGA) databases were utilized for evaluating the expression and prognostic value of CMTM3 through survival data of clinical trials. The enrichment analysis of CMTM3 was performed using the R package “clusterProfiler.” The scores of immune cell infiltration in TCGA samples were downloaded from the ImmuCellAI database and TIMER2 database, and the relationship between both immune cell invasion and CMTM3 expression was investigated. Immunological activation and suppression genes, immune checkpoints, chemokines, and their receptors were all investigated in relation to CMTM3. RESULTS: Most tumor types had varied levels of CMTM3 expression and predicted poor survival status. The CMTM3 expression is closely associated with cancer-associated fibroblasts, macrophages, myeloid dendritic cells, endothelial cells, immune activation genes, immune suppressor genes, immune checkpoints, chemokines, and related receptors. CONCLUSION: Our data reveal that CMTM3 might be used as a cancer biomarker. CMTM3 may work in conjunction with other immunological checkpoints to alter the immune milieu, which could lead to the establishment of new immunotherapy medicines. Hindawi 2022-09-20 /pmc/articles/PMC9553517/ /pubmed/36245970 http://dx.doi.org/10.1155/2022/2103515 Text en Copyright © 2022 Qian Shen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Shen, Qian Cong, Zhirong Zhou, Ying Teng, Yue Gao, Jin Tang, Weiyan CMTM3 as a Potential New Immune Checkpoint Regulator |
title | CMTM3 as a Potential New Immune Checkpoint Regulator |
title_full | CMTM3 as a Potential New Immune Checkpoint Regulator |
title_fullStr | CMTM3 as a Potential New Immune Checkpoint Regulator |
title_full_unstemmed | CMTM3 as a Potential New Immune Checkpoint Regulator |
title_short | CMTM3 as a Potential New Immune Checkpoint Regulator |
title_sort | cmtm3 as a potential new immune checkpoint regulator |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553517/ https://www.ncbi.nlm.nih.gov/pubmed/36245970 http://dx.doi.org/10.1155/2022/2103515 |
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