Cargando…

Identification of a three-miRNA signature as a novel prognostic model for papillary renal cell carcinoma

BACKGROUND: Papillary renal cell carcinoma (pRCC) accounting for near 20% of renal cell carcinoma is the second most common histological subtype. MiRNAs have been demonstrated to played significant roles on predicting prognosis of patients with tumors. An appropriate and comprehensive miRNAs analysi...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Ge, Yang, Haifan, Cheng, Yong, Zhao, Xin, Li, Xu, Jiang, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367267/
https://www.ncbi.nlm.nih.gov/pubmed/32694939
http://dx.doi.org/10.1186/s12935-020-01398-2
_version_ 1783560389482512384
author Li, Ge
Yang, Haifan
Cheng, Yong
Zhao, Xin
Li, Xu
Jiang, Rui
author_facet Li, Ge
Yang, Haifan
Cheng, Yong
Zhao, Xin
Li, Xu
Jiang, Rui
author_sort Li, Ge
collection PubMed
description BACKGROUND: Papillary renal cell carcinoma (pRCC) accounting for near 20% of renal cell carcinoma is the second most common histological subtype. MiRNAs have been demonstrated to played significant roles on predicting prognosis of patients with tumors. An appropriate and comprehensive miRNAs analysis based on a great deal of pRCC samples from The Cancer Genome Atlas (TCGA) will provide perspective in this field. METHODS: We integrated the expression of mRNAs, miRNAs and the relevant clinical data of 321 pRCC patients recorded in the TCGA database. The survival-related differential expressed miRNAs (sDEmiRs) were estimated by COX regression analysis. The high-risk group and the low-risk group were separated by the median risk score of the risk score model (RSM) based on three screened sDEmiRs. The target genes, underlying molecular mechanisms of these sDEmiRs were explored by computational biology. The expression levels of the three sDEmiRs and their correlations with clinicopathological parameters were further validated by qPCR. RESULTS: Based on univariate COX analysis (P < 0.001), eighteen differential expressed miRNAs (DEmiRs) were remarkably related with the overall survival (OS) of pRCC patients. Three sDEmiRs with the most significant prognostic values (miR-34a-5p, miR-410-3p and miR-6720-3p) were employed to establish the RSM which was certified as an independent prognosis factor and closely correlated with OS. In the verification of clinical samples, the overexpression of miR-410-3p and miR-6720-3p were detected to be associated with the advanced T-stages, while miR-34a-5p showed the reversed results. CONCLUSION: The study developed a RSM based on the identified sDEmiRs with significant prognosis prediction values for pRCC patients. The results pave the avenue for establishing and optimizing a reliable and referable risk assessing model and provide novel insight into the researches of biomarkers and clinical treatment strategies.
format Online
Article
Text
id pubmed-7367267
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-73672672020-07-20 Identification of a three-miRNA signature as a novel prognostic model for papillary renal cell carcinoma Li, Ge Yang, Haifan Cheng, Yong Zhao, Xin Li, Xu Jiang, Rui Cancer Cell Int Primary Research BACKGROUND: Papillary renal cell carcinoma (pRCC) accounting for near 20% of renal cell carcinoma is the second most common histological subtype. MiRNAs have been demonstrated to played significant roles on predicting prognosis of patients with tumors. An appropriate and comprehensive miRNAs analysis based on a great deal of pRCC samples from The Cancer Genome Atlas (TCGA) will provide perspective in this field. METHODS: We integrated the expression of mRNAs, miRNAs and the relevant clinical data of 321 pRCC patients recorded in the TCGA database. The survival-related differential expressed miRNAs (sDEmiRs) were estimated by COX regression analysis. The high-risk group and the low-risk group were separated by the median risk score of the risk score model (RSM) based on three screened sDEmiRs. The target genes, underlying molecular mechanisms of these sDEmiRs were explored by computational biology. The expression levels of the three sDEmiRs and their correlations with clinicopathological parameters were further validated by qPCR. RESULTS: Based on univariate COX analysis (P < 0.001), eighteen differential expressed miRNAs (DEmiRs) were remarkably related with the overall survival (OS) of pRCC patients. Three sDEmiRs with the most significant prognostic values (miR-34a-5p, miR-410-3p and miR-6720-3p) were employed to establish the RSM which was certified as an independent prognosis factor and closely correlated with OS. In the verification of clinical samples, the overexpression of miR-410-3p and miR-6720-3p were detected to be associated with the advanced T-stages, while miR-34a-5p showed the reversed results. CONCLUSION: The study developed a RSM based on the identified sDEmiRs with significant prognosis prediction values for pRCC patients. The results pave the avenue for establishing and optimizing a reliable and referable risk assessing model and provide novel insight into the researches of biomarkers and clinical treatment strategies. BioMed Central 2020-07-16 /pmc/articles/PMC7367267/ /pubmed/32694939 http://dx.doi.org/10.1186/s12935-020-01398-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Primary Research
Li, Ge
Yang, Haifan
Cheng, Yong
Zhao, Xin
Li, Xu
Jiang, Rui
Identification of a three-miRNA signature as a novel prognostic model for papillary renal cell carcinoma
title Identification of a three-miRNA signature as a novel prognostic model for papillary renal cell carcinoma
title_full Identification of a three-miRNA signature as a novel prognostic model for papillary renal cell carcinoma
title_fullStr Identification of a three-miRNA signature as a novel prognostic model for papillary renal cell carcinoma
title_full_unstemmed Identification of a three-miRNA signature as a novel prognostic model for papillary renal cell carcinoma
title_short Identification of a three-miRNA signature as a novel prognostic model for papillary renal cell carcinoma
title_sort identification of a three-mirna signature as a novel prognostic model for papillary renal cell carcinoma
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367267/
https://www.ncbi.nlm.nih.gov/pubmed/32694939
http://dx.doi.org/10.1186/s12935-020-01398-2
work_keys_str_mv AT lige identificationofathreemirnasignatureasanovelprognosticmodelforpapillaryrenalcellcarcinoma
AT yanghaifan identificationofathreemirnasignatureasanovelprognosticmodelforpapillaryrenalcellcarcinoma
AT chengyong identificationofathreemirnasignatureasanovelprognosticmodelforpapillaryrenalcellcarcinoma
AT zhaoxin identificationofathreemirnasignatureasanovelprognosticmodelforpapillaryrenalcellcarcinoma
AT lixu identificationofathreemirnasignatureasanovelprognosticmodelforpapillaryrenalcellcarcinoma
AT jiangrui identificationofathreemirnasignatureasanovelprognosticmodelforpapillaryrenalcellcarcinoma