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Gene Characteristics and Prognostic Values of m(6)A RNA Methylation Regulators in Nonsmall Cell Lung Cancer

BACKGROUND: N(6)-methyladenosine (m(6)A) is the most common internal modification present in mRNAs and long noncoding RNAs (lncRNAs), associated with tumorigenesis and cancer progression. However, little is known about the roles of m(6)A and its regulatory genes in nonsmall cell lung cancer (NSCLC)....

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Autores principales: Li, Na, Chen, Xiaojuan, Liu, Yanhong, Zhou, Tieming, Li, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346307/
https://www.ncbi.nlm.nih.gov/pubmed/34367534
http://dx.doi.org/10.1155/2021/2257066
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author Li, Na
Chen, Xiaojuan
Liu, Yanhong
Zhou, Tieming
Li, Wei
author_facet Li, Na
Chen, Xiaojuan
Liu, Yanhong
Zhou, Tieming
Li, Wei
author_sort Li, Na
collection PubMed
description BACKGROUND: N(6)-methyladenosine (m(6)A) is the most common internal modification present in mRNAs and long noncoding RNAs (lncRNAs), associated with tumorigenesis and cancer progression. However, little is known about the roles of m(6)A and its regulatory genes in nonsmall cell lung cancer (NSCLC). Here, we systematically explored the roles and prognostic significance of m(6)A-associated regulatory genes in NSCLC. METHODS: The copy number variation (CNV), mutation, mRNA expression data, and corresponding clinical pathology information of 1057 NSCLC patients were downloaded from the cancer genome atlas (TCGA) database. The gain and loss levels of CNVs were determined by utilizing segmentation analysis and GISTIC algorithm. The GSEA was conducted to explore the functions related to different levels of m(6)A regulatory genes. Logrank test was utilized to assess the prognostic significance of m(6)A-related gene's CNV. RESULTS: The genetic alterations of ten m(6)A-associated regulators were identified in 102 independent NSCLC samples and significantly related to advanced tumor stage. Deletions or shallow deletions corresponded to lower mRNA expression while copy number gains or amplifications were related to increased mRNA expression of m(6)A regulatory genes. Survival analysis showed the patients with copy number loss of FTO with worse disease-free survival (DFS) or overall survival (OS). Besides, copy number loss of YTHDC2 was also with poor OS for NSCLC patients. Moreover, high FTO expression was significantly associated with oxidative phosphorylation, translation, and metabolism of mRNA. CONCLUSION: Our findings provide novel insight for better understanding of the roles of m(6)A regulators and RNA epigenetic modification in the pathogenesis of NSCLC.
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spelling pubmed-83463072021-08-07 Gene Characteristics and Prognostic Values of m(6)A RNA Methylation Regulators in Nonsmall Cell Lung Cancer Li, Na Chen, Xiaojuan Liu, Yanhong Zhou, Tieming Li, Wei J Healthc Eng Research Article BACKGROUND: N(6)-methyladenosine (m(6)A) is the most common internal modification present in mRNAs and long noncoding RNAs (lncRNAs), associated with tumorigenesis and cancer progression. However, little is known about the roles of m(6)A and its regulatory genes in nonsmall cell lung cancer (NSCLC). Here, we systematically explored the roles and prognostic significance of m(6)A-associated regulatory genes in NSCLC. METHODS: The copy number variation (CNV), mutation, mRNA expression data, and corresponding clinical pathology information of 1057 NSCLC patients were downloaded from the cancer genome atlas (TCGA) database. The gain and loss levels of CNVs were determined by utilizing segmentation analysis and GISTIC algorithm. The GSEA was conducted to explore the functions related to different levels of m(6)A regulatory genes. Logrank test was utilized to assess the prognostic significance of m(6)A-related gene's CNV. RESULTS: The genetic alterations of ten m(6)A-associated regulators were identified in 102 independent NSCLC samples and significantly related to advanced tumor stage. Deletions or shallow deletions corresponded to lower mRNA expression while copy number gains or amplifications were related to increased mRNA expression of m(6)A regulatory genes. Survival analysis showed the patients with copy number loss of FTO with worse disease-free survival (DFS) or overall survival (OS). Besides, copy number loss of YTHDC2 was also with poor OS for NSCLC patients. Moreover, high FTO expression was significantly associated with oxidative phosphorylation, translation, and metabolism of mRNA. CONCLUSION: Our findings provide novel insight for better understanding of the roles of m(6)A regulators and RNA epigenetic modification in the pathogenesis of NSCLC. Hindawi 2021-07-29 /pmc/articles/PMC8346307/ /pubmed/34367534 http://dx.doi.org/10.1155/2021/2257066 Text en Copyright © 2021 Na Li 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
Li, Na
Chen, Xiaojuan
Liu, Yanhong
Zhou, Tieming
Li, Wei
Gene Characteristics and Prognostic Values of m(6)A RNA Methylation Regulators in Nonsmall Cell Lung Cancer
title Gene Characteristics and Prognostic Values of m(6)A RNA Methylation Regulators in Nonsmall Cell Lung Cancer
title_full Gene Characteristics and Prognostic Values of m(6)A RNA Methylation Regulators in Nonsmall Cell Lung Cancer
title_fullStr Gene Characteristics and Prognostic Values of m(6)A RNA Methylation Regulators in Nonsmall Cell Lung Cancer
title_full_unstemmed Gene Characteristics and Prognostic Values of m(6)A RNA Methylation Regulators in Nonsmall Cell Lung Cancer
title_short Gene Characteristics and Prognostic Values of m(6)A RNA Methylation Regulators in Nonsmall Cell Lung Cancer
title_sort gene characteristics and prognostic values of m(6)a rna methylation regulators in nonsmall cell lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346307/
https://www.ncbi.nlm.nih.gov/pubmed/34367534
http://dx.doi.org/10.1155/2021/2257066
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