Identification of a Four-lncRNA Prognostic Signature for Colon Cancer Based on Genome Instability

LncRNAs (long noncoding RNAs) are closely associated with genome instability. However, the identification of lncRNAs related to the genome instability and their relationship with the prognosis and clinical signature of cancer remains to be explored. In this paper, we analyzed differential lncRNA exp...

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Main Authors: Duo Yun, Zhirong Yang
Format: Article
Language:English
Published: Hindawi Limited 2021-01-01
Series:Journal of Oncology
Online Access:http://dx.doi.org/10.1155/2021/7408893
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spelling doaj-cd1d1d39c7d14b2ca9730778be3eacb02021-10-04T01:57:33ZengHindawi LimitedJournal of Oncology1687-84692021-01-01202110.1155/2021/7408893Identification of a Four-lncRNA Prognostic Signature for Colon Cancer Based on Genome InstabilityDuo Yun0Zhirong Yang1Inner Mongolia Yuanhe Mongolian Traditional Medicine Research InstituteDepartment of SurgicalLncRNAs (long noncoding RNAs) are closely associated with genome instability. However, the identification of lncRNAs related to the genome instability and their relationship with the prognosis and clinical signature of cancer remains to be explored. In this paper, we analyzed differential lncRNA expression based on the somatic mutation profiles of colon cancer patients from TCGA database and finally identified 153 lncRNAs that are associated with genome instability in colon cancer. Taking four lncRNAs from these 153, we established a genome-instability-related prognostic signature (GIRlncPSig). By applying the GIRlncPSig, we calculated a risk score for each patient, and using their risk scores, we divided them into low- and high-risk groups. We found that the prognosis between the two risk groups was significantly different, and the results were further verified in different independent patient cohorts. Moreover, we observed that the GIRlncPSig was related to somatic mutation rates in colon cancer, indicating that it may be a potential means of measuring genome instability levels in colon cancer. We also revealed that the GIRlncPSig was correlated with BRAF and DPYD mutation rates and that it may be a potential mutation marker for the BRAF and DPYD gene. In summary, we constructed a genome-instability-related lncRNA prognostic signature (GIRlncPSig), which has a significant effect on prognosis prediction and may allow for the discovery of new colon cancer biomarkers.http://dx.doi.org/10.1155/2021/7408893
collection DOAJ
language English
format Article
sources DOAJ
author Duo Yun
Zhirong Yang
spellingShingle Duo Yun
Zhirong Yang
Identification of a Four-lncRNA Prognostic Signature for Colon Cancer Based on Genome Instability
Journal of Oncology
author_facet Duo Yun
Zhirong Yang
author_sort Duo Yun
title Identification of a Four-lncRNA Prognostic Signature for Colon Cancer Based on Genome Instability
title_short Identification of a Four-lncRNA Prognostic Signature for Colon Cancer Based on Genome Instability
title_full Identification of a Four-lncRNA Prognostic Signature for Colon Cancer Based on Genome Instability
title_fullStr Identification of a Four-lncRNA Prognostic Signature for Colon Cancer Based on Genome Instability
title_full_unstemmed Identification of a Four-lncRNA Prognostic Signature for Colon Cancer Based on Genome Instability
title_sort identification of a four-lncrna prognostic signature for colon cancer based on genome instability
publisher Hindawi Limited
series Journal of Oncology
issn 1687-8469
publishDate 2021-01-01
description LncRNAs (long noncoding RNAs) are closely associated with genome instability. However, the identification of lncRNAs related to the genome instability and their relationship with the prognosis and clinical signature of cancer remains to be explored. In this paper, we analyzed differential lncRNA expression based on the somatic mutation profiles of colon cancer patients from TCGA database and finally identified 153 lncRNAs that are associated with genome instability in colon cancer. Taking four lncRNAs from these 153, we established a genome-instability-related prognostic signature (GIRlncPSig). By applying the GIRlncPSig, we calculated a risk score for each patient, and using their risk scores, we divided them into low- and high-risk groups. We found that the prognosis between the two risk groups was significantly different, and the results were further verified in different independent patient cohorts. Moreover, we observed that the GIRlncPSig was related to somatic mutation rates in colon cancer, indicating that it may be a potential means of measuring genome instability levels in colon cancer. We also revealed that the GIRlncPSig was correlated with BRAF and DPYD mutation rates and that it may be a potential mutation marker for the BRAF and DPYD gene. In summary, we constructed a genome-instability-related lncRNA prognostic signature (GIRlncPSig), which has a significant effect on prognosis prediction and may allow for the discovery of new colon cancer biomarkers.
url http://dx.doi.org/10.1155/2021/7408893
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AT zhirongyang identificationofafourlncrnaprognosticsignatureforcoloncancerbasedongenomeinstability
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