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Role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers

N6-methyladenosine (m6A) modifications can be found in eukaryotic messenger RNA (mRNA), long non-coding RNA (lncRNA), and microRNA (miRNA). Several studies have demonstrated a close relationship between m6A modifications and cancer cells. Methyltransferase-like enzyme 3 (METTL3) and methyltransferas...

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Autores principales: Tao, Zijia, Zhao, Yiqiao, Chen, Xiaonan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382367/
https://www.ncbi.nlm.nih.gov/pubmed/32765970
http://dx.doi.org/10.7717/peerj.9589
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author Tao, Zijia
Zhao, Yiqiao
Chen, Xiaonan
author_facet Tao, Zijia
Zhao, Yiqiao
Chen, Xiaonan
author_sort Tao, Zijia
collection PubMed
description N6-methyladenosine (m6A) modifications can be found in eukaryotic messenger RNA (mRNA), long non-coding RNA (lncRNA), and microRNA (miRNA). Several studies have demonstrated a close relationship between m6A modifications and cancer cells. Methyltransferase-like enzyme 3 (METTL3) and methyltransferase-like enzyme 14 (METTL14) are two major enzymes involved in m6A modifications that play vital roles in various cancers. However, the roles and regulatory mechanisms of METTL3 and METTL14 in urological cancers are largely unknown. In this review, we summarize the current research results for METTL3 and METTL14 and identify potential pathways involving these enzymes in kidney, bladder, prostate, and testicular cancer. We found that METTL3 and METTL14 have different expression patterns in four types of urological cancers. METTL3 is highly expressed in bladder and prostate cancer and plays an oncogenic role on cancer cells; however, its expression and role are opposite in kidney cancer. METTL14 is expressed at low levels in kidney and bladder cancer, where it has a tumor suppressive role. Low METTL3 or METTL14 expression in cancer cells negatively regulates cell growth-related pathways (e.g., mTOR, EMT, and P2XR6) but positively regulates cell death-related pathways (e.g., P53, PTEN, and Notch1). When METTL3 is highly expressed, it positively regulates the NF-kB and SHH-GL1pathways but negatively regulates PTEN. These results suggest that although METTL3 and METTL14 have different expression levels and regulatory mechanisms in urological cancers, they control cancer cell fate via cell growth- and cell death-related pathways. These findings suggest that m6A modification may be a potential new therapeutic target in urological cancer.
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spelling pubmed-73823672020-08-05 Role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers Tao, Zijia Zhao, Yiqiao Chen, Xiaonan PeerJ Molecular Biology N6-methyladenosine (m6A) modifications can be found in eukaryotic messenger RNA (mRNA), long non-coding RNA (lncRNA), and microRNA (miRNA). Several studies have demonstrated a close relationship between m6A modifications and cancer cells. Methyltransferase-like enzyme 3 (METTL3) and methyltransferase-like enzyme 14 (METTL14) are two major enzymes involved in m6A modifications that play vital roles in various cancers. However, the roles and regulatory mechanisms of METTL3 and METTL14 in urological cancers are largely unknown. In this review, we summarize the current research results for METTL3 and METTL14 and identify potential pathways involving these enzymes in kidney, bladder, prostate, and testicular cancer. We found that METTL3 and METTL14 have different expression patterns in four types of urological cancers. METTL3 is highly expressed in bladder and prostate cancer and plays an oncogenic role on cancer cells; however, its expression and role are opposite in kidney cancer. METTL14 is expressed at low levels in kidney and bladder cancer, where it has a tumor suppressive role. Low METTL3 or METTL14 expression in cancer cells negatively regulates cell growth-related pathways (e.g., mTOR, EMT, and P2XR6) but positively regulates cell death-related pathways (e.g., P53, PTEN, and Notch1). When METTL3 is highly expressed, it positively regulates the NF-kB and SHH-GL1pathways but negatively regulates PTEN. These results suggest that although METTL3 and METTL14 have different expression levels and regulatory mechanisms in urological cancers, they control cancer cell fate via cell growth- and cell death-related pathways. These findings suggest that m6A modification may be a potential new therapeutic target in urological cancer. PeerJ Inc. 2020-07-22 /pmc/articles/PMC7382367/ /pubmed/32765970 http://dx.doi.org/10.7717/peerj.9589 Text en ©2020 Tao et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Molecular Biology
Tao, Zijia
Zhao, Yiqiao
Chen, Xiaonan
Role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers
title Role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers
title_full Role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers
title_fullStr Role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers
title_full_unstemmed Role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers
title_short Role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers
title_sort role of methyltransferase-like enzyme 3 and methyltransferase-like enzyme 14 in urological cancers
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382367/
https://www.ncbi.nlm.nih.gov/pubmed/32765970
http://dx.doi.org/10.7717/peerj.9589
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