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Comprehensive Characterization of Common and Cancer-Specific Differently Expressed lncRNAs in Urologic Cancers

Urologic cancers, comprising prostate carcinoma (PCa), renal cell carcinoma (RCC), and bladder carcinoma (BCa), were the commonly occurred carcinoma amid males. Long noncoding RNAs (lncRNAs) with the length of more than 200 nt functioned importantly in physiological and pathological advancement. Nev...

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Autores principales: Yan, You-Ji, Zhang, Ling, Zhou, Jia-Jie, Chen, Zhong-Jun, Liao, Yi-Xiang, Zeng, Jin-Min, Shen, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286197/
https://www.ncbi.nlm.nih.gov/pubmed/34335862
http://dx.doi.org/10.1155/2021/5515218
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author Yan, You-Ji
Zhang, Ling
Zhou, Jia-Jie
Chen, Zhong-Jun
Liao, Yi-Xiang
Zeng, Jin-Min
Shen, Hao
author_facet Yan, You-Ji
Zhang, Ling
Zhou, Jia-Jie
Chen, Zhong-Jun
Liao, Yi-Xiang
Zeng, Jin-Min
Shen, Hao
author_sort Yan, You-Ji
collection PubMed
description Urologic cancers, comprising prostate carcinoma (PCa), renal cell carcinoma (RCC), and bladder carcinoma (BCa), were the commonly occurred carcinoma amid males. Long noncoding RNAs (lncRNAs) with the length of more than 200 nt functioned importantly in physiological and pathological advancement. Nevertheless, further investigation regarding lncRNA expression feature and function in urologic cancers should be essential. This study is aimed at uncovering the roles of the differently expressed lncRNAs in urologic cancers. The data of gene expression levels was downloaded from lncRNAtor datasets. The lncRNA expression pattern existing in different urologic cancers was assessed by hierarchical clustering analysis. Gene Ontology (GO) analysis and KEGG pathway analysis were separately applied to evaluate the biological function and process and the biological pathways involving differently expressed lncRNAs. Our results indicated that 18 lncRNA expressions were increased, and 16 lncRNA expressions were reduced in urologic cancers after comparison with that in normal tissues. Moreover, our results demonstrated 61, 422, 137, and 281 lncRNAs were specifically dysregulated in bladder cancer (BLCA), kidney renal clear cell cancer (KIRC), kidney renal papillary cell cancer (KIRP), and prostate adenocarcinoma (PRAD), respectively. Bioinformatics analysis showed that differently expressed lncRNAs displayed crucially in urologic cancers. The prognostic value of common and cancer-specific differently expressed lncRNAs, such as PVT1, in cancer outcomes, was emphasized here. Our research has deeply unearthed the mechanism of differently expressed lncRNAs in urologic cancers development.
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spelling pubmed-82861972021-07-30 Comprehensive Characterization of Common and Cancer-Specific Differently Expressed lncRNAs in Urologic Cancers Yan, You-Ji Zhang, Ling Zhou, Jia-Jie Chen, Zhong-Jun Liao, Yi-Xiang Zeng, Jin-Min Shen, Hao Comput Math Methods Med Research Article Urologic cancers, comprising prostate carcinoma (PCa), renal cell carcinoma (RCC), and bladder carcinoma (BCa), were the commonly occurred carcinoma amid males. Long noncoding RNAs (lncRNAs) with the length of more than 200 nt functioned importantly in physiological and pathological advancement. Nevertheless, further investigation regarding lncRNA expression feature and function in urologic cancers should be essential. This study is aimed at uncovering the roles of the differently expressed lncRNAs in urologic cancers. The data of gene expression levels was downloaded from lncRNAtor datasets. The lncRNA expression pattern existing in different urologic cancers was assessed by hierarchical clustering analysis. Gene Ontology (GO) analysis and KEGG pathway analysis were separately applied to evaluate the biological function and process and the biological pathways involving differently expressed lncRNAs. Our results indicated that 18 lncRNA expressions were increased, and 16 lncRNA expressions were reduced in urologic cancers after comparison with that in normal tissues. Moreover, our results demonstrated 61, 422, 137, and 281 lncRNAs were specifically dysregulated in bladder cancer (BLCA), kidney renal clear cell cancer (KIRC), kidney renal papillary cell cancer (KIRP), and prostate adenocarcinoma (PRAD), respectively. Bioinformatics analysis showed that differently expressed lncRNAs displayed crucially in urologic cancers. The prognostic value of common and cancer-specific differently expressed lncRNAs, such as PVT1, in cancer outcomes, was emphasized here. Our research has deeply unearthed the mechanism of differently expressed lncRNAs in urologic cancers development. Hindawi 2021-07-09 /pmc/articles/PMC8286197/ /pubmed/34335862 http://dx.doi.org/10.1155/2021/5515218 Text en Copyright © 2021 You-Ji Yan 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
Yan, You-Ji
Zhang, Ling
Zhou, Jia-Jie
Chen, Zhong-Jun
Liao, Yi-Xiang
Zeng, Jin-Min
Shen, Hao
Comprehensive Characterization of Common and Cancer-Specific Differently Expressed lncRNAs in Urologic Cancers
title Comprehensive Characterization of Common and Cancer-Specific Differently Expressed lncRNAs in Urologic Cancers
title_full Comprehensive Characterization of Common and Cancer-Specific Differently Expressed lncRNAs in Urologic Cancers
title_fullStr Comprehensive Characterization of Common and Cancer-Specific Differently Expressed lncRNAs in Urologic Cancers
title_full_unstemmed Comprehensive Characterization of Common and Cancer-Specific Differently Expressed lncRNAs in Urologic Cancers
title_short Comprehensive Characterization of Common and Cancer-Specific Differently Expressed lncRNAs in Urologic Cancers
title_sort comprehensive characterization of common and cancer-specific differently expressed lncrnas in urologic cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286197/
https://www.ncbi.nlm.nih.gov/pubmed/34335862
http://dx.doi.org/10.1155/2021/5515218
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