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MicroRNA-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer

INTRODUCTION: High relapse rate of nonmuscle invasive bladder cancer (NMIBC) is a major challenge. Overexpression of microRNA-21 (miR-21) which targets phosphatase and tensin homolog (PTEN), a gene associated with malignancy, has been reported in the bladder tumor tissue compared to normal mucosa by...

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Autores principales: Mitash, Nilay, Agnihotri, Shalini, Tiwari, Swasti, Agrawal, Vinita, Mandhani, Anil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635668/
https://www.ncbi.nlm.nih.gov/pubmed/29021651
http://dx.doi.org/10.4103/iju.IJU_4_17
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author Mitash, Nilay
Agnihotri, Shalini
Tiwari, Swasti
Agrawal, Vinita
Mandhani, Anil
author_facet Mitash, Nilay
Agnihotri, Shalini
Tiwari, Swasti
Agrawal, Vinita
Mandhani, Anil
author_sort Mitash, Nilay
collection PubMed
description INTRODUCTION: High relapse rate of nonmuscle invasive bladder cancer (NMIBC) is a major challenge. Overexpression of microRNA-21 (miR-21) which targets phosphatase and tensin homolog (PTEN), a gene associated with malignancy, has been reported in the bladder tumor tissue compared to normal mucosa by us and others. We have tested whether miR-21 levels in bladder mucosa could predict tumor recurrence. METHODS: In a prospective cohort setting, tumor tissues and normal bladder mucosa (NBM) were taken from BC patients during transurethral resection of bladder tumor. Age- and ethnicity-matched NBM from benign prostate hyperplasia patients was taken as controls. The expression of miR-21 was analyzed using quantitative reverse transcription polymerase chain reaction. Patients were followed for 4 years for tumor reoccurrence. Postoperative recurrence were recorded and calculated by Kaplan–Meier curve. RESULTS: In 31 patients, miR-21 was up-regulated (>4-fold, P = 0.003), and PTEN levels were significantly lower (<7-folds, P = 0.001) in tumor tissue relative to NBM. Moreover, the fold change in miR-21 levels was significantly higher (>3-folds, P = 0.03) in patients showing recurrence compared to those in which tumor did not recur. Further, Kaplan–Meier analysis shows overexpression of miR-21 corresponds to less time to recurrence with higher cumulative hazard. CONCLUSION: We found overexpression of miR-21 in tumor tissue and its association with recurrence, time to recurrence and invasiveness in BC. Quantification of miR-21 along with other pathological parameters could be more objective molecular approach to predict recurrence in NMIBC.
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spelling pubmed-56356682017-10-11 MicroRNA-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer Mitash, Nilay Agnihotri, Shalini Tiwari, Swasti Agrawal, Vinita Mandhani, Anil Indian J Urol Original Article INTRODUCTION: High relapse rate of nonmuscle invasive bladder cancer (NMIBC) is a major challenge. Overexpression of microRNA-21 (miR-21) which targets phosphatase and tensin homolog (PTEN), a gene associated with malignancy, has been reported in the bladder tumor tissue compared to normal mucosa by us and others. We have tested whether miR-21 levels in bladder mucosa could predict tumor recurrence. METHODS: In a prospective cohort setting, tumor tissues and normal bladder mucosa (NBM) were taken from BC patients during transurethral resection of bladder tumor. Age- and ethnicity-matched NBM from benign prostate hyperplasia patients was taken as controls. The expression of miR-21 was analyzed using quantitative reverse transcription polymerase chain reaction. Patients were followed for 4 years for tumor reoccurrence. Postoperative recurrence were recorded and calculated by Kaplan–Meier curve. RESULTS: In 31 patients, miR-21 was up-regulated (>4-fold, P = 0.003), and PTEN levels were significantly lower (<7-folds, P = 0.001) in tumor tissue relative to NBM. Moreover, the fold change in miR-21 levels was significantly higher (>3-folds, P = 0.03) in patients showing recurrence compared to those in which tumor did not recur. Further, Kaplan–Meier analysis shows overexpression of miR-21 corresponds to less time to recurrence with higher cumulative hazard. CONCLUSION: We found overexpression of miR-21 in tumor tissue and its association with recurrence, time to recurrence and invasiveness in BC. Quantification of miR-21 along with other pathological parameters could be more objective molecular approach to predict recurrence in NMIBC. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5635668/ /pubmed/29021651 http://dx.doi.org/10.4103/iju.IJU_4_17 Text en Copyright: © 2017 Indian Journal of Urology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Mitash, Nilay
Agnihotri, Shalini
Tiwari, Swasti
Agrawal, Vinita
Mandhani, Anil
MicroRNA-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer
title MicroRNA-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer
title_full MicroRNA-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer
title_fullStr MicroRNA-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer
title_full_unstemmed MicroRNA-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer
title_short MicroRNA-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer
title_sort microrna-21 could be a molecular marker to predict the recurrence of nonmuscle invasive bladder cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635668/
https://www.ncbi.nlm.nih.gov/pubmed/29021651
http://dx.doi.org/10.4103/iju.IJU_4_17
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