Screening and Identifying m6A Regulators as an Independent Prognostic Biomarker in Pancreatic Cancer Based on The Cancer Genome Atlas Database
Background. Pancreatic cancer is one of the most malignant tumors of the digestive system, and its treatment has rarely progressed for the last two decades. Studies on m6A regulators for the past few years have seemingly provided a novel approach for malignant tumor therapy. m6A-related factors may...
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2021-01-01
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Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2021/5573628 |
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doaj-cde7f9ec00d843098bf08f265d389aa12021-05-31T00:33:48ZengHindawi LimitedBioMed Research International2314-61412021-01-01202110.1155/2021/5573628Screening and Identifying m6A Regulators as an Independent Prognostic Biomarker in Pancreatic Cancer Based on The Cancer Genome Atlas DatabaseBi Lin0Yangyang Pan1Dinglai Yu2Shengjie Dai3Hongwei Sun4Shengchuan Chen5Jie Zhang6Yukai Xiang7Chaohao Huang8Department of AnesthesiologyDepartment of Emergency MedicineDepartment of Hepatological SurgeryDepartment of Hepatological SurgeryDepartment of Hepatological SurgeryDepartment of Hepatological SurgeryDepartment of Hepatological SurgeryDepartment of Hepatological SurgeryDepartment of Hepatological SurgeryBackground. Pancreatic cancer is one of the most malignant tumors of the digestive system, and its treatment has rarely progressed for the last two decades. Studies on m6A regulators for the past few years have seemingly provided a novel approach for malignant tumor therapy. m6A-related factors may be potential biomarkers and therapeutic targets. This research is focused on the gene characteristics and clinical values of m6A regulators in predicting prognosis in pancreatic cancer. Methods. In our study, we obtained gene expression profiles with copy number variation (CNV) data and clinical characteristic data of 186 patients with pancreatic cancer from The Cancer Genome Atlas (TCGA) portal. Then, we determined the alteration of m6a regulators and their correlation with clinicopathological features using the log-rank tests, Cox regression model, and chi-square test. Additionally, we validated the prognostic value of m6A regulators in the International Cancer Genome Consortium (ICGC). Results. The results suggested that pancreatic cancer patients with ALKBH5 CNV were associated with worse overall survival and disease-free survival than those with diploid genes. Additionally, upregulation of the writer gene ALKBH5 had a positive correlation with the activation of AKT pathways in the TCGA database. Conclusion. Our study not only demonstrated genetic characteristic changes of m6A-related genes in pancreatic cancer and found a strong relationship between the changes of ALKBH5 and poor prognosis but also provided a novel therapeutic target for pancreatic cancer therapy.http://dx.doi.org/10.1155/2021/5573628 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Bi Lin Yangyang Pan Dinglai Yu Shengjie Dai Hongwei Sun Shengchuan Chen Jie Zhang Yukai Xiang Chaohao Huang |
spellingShingle |
Bi Lin Yangyang Pan Dinglai Yu Shengjie Dai Hongwei Sun Shengchuan Chen Jie Zhang Yukai Xiang Chaohao Huang Screening and Identifying m6A Regulators as an Independent Prognostic Biomarker in Pancreatic Cancer Based on The Cancer Genome Atlas Database BioMed Research International |
author_facet |
Bi Lin Yangyang Pan Dinglai Yu Shengjie Dai Hongwei Sun Shengchuan Chen Jie Zhang Yukai Xiang Chaohao Huang |
author_sort |
Bi Lin |
title |
Screening and Identifying m6A Regulators as an Independent Prognostic Biomarker in Pancreatic Cancer Based on The Cancer Genome Atlas Database |
title_short |
Screening and Identifying m6A Regulators as an Independent Prognostic Biomarker in Pancreatic Cancer Based on The Cancer Genome Atlas Database |
title_full |
Screening and Identifying m6A Regulators as an Independent Prognostic Biomarker in Pancreatic Cancer Based on The Cancer Genome Atlas Database |
title_fullStr |
Screening and Identifying m6A Regulators as an Independent Prognostic Biomarker in Pancreatic Cancer Based on The Cancer Genome Atlas Database |
title_full_unstemmed |
Screening and Identifying m6A Regulators as an Independent Prognostic Biomarker in Pancreatic Cancer Based on The Cancer Genome Atlas Database |
title_sort |
screening and identifying m6a regulators as an independent prognostic biomarker in pancreatic cancer based on the cancer genome atlas database |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6141 |
publishDate |
2021-01-01 |
description |
Background. Pancreatic cancer is one of the most malignant tumors of the digestive system, and its treatment has rarely progressed for the last two decades. Studies on m6A regulators for the past few years have seemingly provided a novel approach for malignant tumor therapy. m6A-related factors may be potential biomarkers and therapeutic targets. This research is focused on the gene characteristics and clinical values of m6A regulators in predicting prognosis in pancreatic cancer. Methods. In our study, we obtained gene expression profiles with copy number variation (CNV) data and clinical characteristic data of 186 patients with pancreatic cancer from The Cancer Genome Atlas (TCGA) portal. Then, we determined the alteration of m6a regulators and their correlation with clinicopathological features using the log-rank tests, Cox regression model, and chi-square test. Additionally, we validated the prognostic value of m6A regulators in the International Cancer Genome Consortium (ICGC). Results. The results suggested that pancreatic cancer patients with ALKBH5 CNV were associated with worse overall survival and disease-free survival than those with diploid genes. Additionally, upregulation of the writer gene ALKBH5 had a positive correlation with the activation of AKT pathways in the TCGA database. Conclusion. Our study not only demonstrated genetic characteristic changes of m6A-related genes in pancreatic cancer and found a strong relationship between the changes of ALKBH5 and poor prognosis but also provided a novel therapeutic target for pancreatic cancer therapy. |
url |
http://dx.doi.org/10.1155/2021/5573628 |
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