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M6A “Writer” Gene METTL14: A Favorable Prognostic Biomarker and Correlated With Immune Infiltrates in Rectal Cancer
Rectal cancer (RC) is the leading cause of tumor-related death among both men and women. The efficacy of immunotherapy for rectal cancer is closely related to the immune infiltration level. The N6-methyladenosine (m6A) modification may play a pivotal role in tumor-immune interactions. However, the r...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247640/ https://www.ncbi.nlm.nih.gov/pubmed/34221955 http://dx.doi.org/10.3389/fonc.2021.615296 |
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author | Cai, Changjing Long, Jie Huang, Qiaoqiao Han, Ying Peng, Yinghui Guo, Cao Liu, Shanshan Chen, Yihong Shen, Edward Long, Kexin Wang, Xinwen Yu, Jian Shen, Hong Zeng, Shan |
author_facet | Cai, Changjing Long, Jie Huang, Qiaoqiao Han, Ying Peng, Yinghui Guo, Cao Liu, Shanshan Chen, Yihong Shen, Edward Long, Kexin Wang, Xinwen Yu, Jian Shen, Hong Zeng, Shan |
author_sort | Cai, Changjing |
collection | PubMed |
description | Rectal cancer (RC) is the leading cause of tumor-related death among both men and women. The efficacy of immunotherapy for rectal cancer is closely related to the immune infiltration level. The N6-methyladenosine (m6A) modification may play a pivotal role in tumor-immune interactions. However, the roles of m6A-related genes in tumor-immune interactions of rectal cancer remain largely unknown. After an evaluation on the expression levels of m6A-related genes and their correlations with the prognosis of rectal cancer patients, we found that METTL14 was the only gene to be significantly correlated with prognosis in rectal cancer patients. Therefore, we further observed the impact of METTL14 expression and m6A modification on the immune infiltration in rectal cancer. Our study indicates that low expression of the m6A “writer” gene METTL14 in rectal cancer may lead to the downregulation of m6A RNA modification, thus reducing the level of immune cell infiltration and resulting in poor prognosis. METTL14 expression level is an independent prognostic factor in rectal cancer and is positively correlated with the immune infiltration level. Our study identified METTL14 as a potential target for enhancing immunotherapy efficacy in rectal cancer. |
format | Online Article Text |
id | pubmed-8247640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82476402021-07-02 M6A “Writer” Gene METTL14: A Favorable Prognostic Biomarker and Correlated With Immune Infiltrates in Rectal Cancer Cai, Changjing Long, Jie Huang, Qiaoqiao Han, Ying Peng, Yinghui Guo, Cao Liu, Shanshan Chen, Yihong Shen, Edward Long, Kexin Wang, Xinwen Yu, Jian Shen, Hong Zeng, Shan Front Oncol Oncology Rectal cancer (RC) is the leading cause of tumor-related death among both men and women. The efficacy of immunotherapy for rectal cancer is closely related to the immune infiltration level. The N6-methyladenosine (m6A) modification may play a pivotal role in tumor-immune interactions. However, the roles of m6A-related genes in tumor-immune interactions of rectal cancer remain largely unknown. After an evaluation on the expression levels of m6A-related genes and their correlations with the prognosis of rectal cancer patients, we found that METTL14 was the only gene to be significantly correlated with prognosis in rectal cancer patients. Therefore, we further observed the impact of METTL14 expression and m6A modification on the immune infiltration in rectal cancer. Our study indicates that low expression of the m6A “writer” gene METTL14 in rectal cancer may lead to the downregulation of m6A RNA modification, thus reducing the level of immune cell infiltration and resulting in poor prognosis. METTL14 expression level is an independent prognostic factor in rectal cancer and is positively correlated with the immune infiltration level. Our study identified METTL14 as a potential target for enhancing immunotherapy efficacy in rectal cancer. Frontiers Media S.A. 2021-06-17 /pmc/articles/PMC8247640/ /pubmed/34221955 http://dx.doi.org/10.3389/fonc.2021.615296 Text en Copyright © 2021 Cai, Long, Huang, Han, Peng, Guo, Liu, Chen, Shen, Long, Wang, Yu, Shen and Zeng 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 | Oncology Cai, Changjing Long, Jie Huang, Qiaoqiao Han, Ying Peng, Yinghui Guo, Cao Liu, Shanshan Chen, Yihong Shen, Edward Long, Kexin Wang, Xinwen Yu, Jian Shen, Hong Zeng, Shan M6A “Writer” Gene METTL14: A Favorable Prognostic Biomarker and Correlated With Immune Infiltrates in Rectal Cancer |
title | M6A “Writer” Gene METTL14: A Favorable Prognostic Biomarker and Correlated With Immune Infiltrates in Rectal Cancer |
title_full | M6A “Writer” Gene METTL14: A Favorable Prognostic Biomarker and Correlated With Immune Infiltrates in Rectal Cancer |
title_fullStr | M6A “Writer” Gene METTL14: A Favorable Prognostic Biomarker and Correlated With Immune Infiltrates in Rectal Cancer |
title_full_unstemmed | M6A “Writer” Gene METTL14: A Favorable Prognostic Biomarker and Correlated With Immune Infiltrates in Rectal Cancer |
title_short | M6A “Writer” Gene METTL14: A Favorable Prognostic Biomarker and Correlated With Immune Infiltrates in Rectal Cancer |
title_sort | m6a “writer” gene mettl14: a favorable prognostic biomarker and correlated with immune infiltrates in rectal cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247640/ https://www.ncbi.nlm.nih.gov/pubmed/34221955 http://dx.doi.org/10.3389/fonc.2021.615296 |
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