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Decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy

The identification and development of biomarkers which predict response of muscle invasive bladder cancer (MIBC) patients to neoadjuvant chemotherapy would likely increase usage of this treatment option and thereby improve patient survival rates. MiRNA array and qRT-PCR validation was used to identi...

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Autores principales: Vinall, Ruth L., Tepper, Clifford G., Ripoll, Alexandra A. Z., Gandour-Edwards, Regina F., Durbin-Johnson, Blythe P., Yap, Stanley A., Ghosh, Paramita M., deVere White, Ralph W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918947/
https://www.ncbi.nlm.nih.gov/pubmed/27382433
http://dx.doi.org/10.18632/genesandcancer.103
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author Vinall, Ruth L.
Tepper, Clifford G.
Ripoll, Alexandra A. Z.
Gandour-Edwards, Regina F.
Durbin-Johnson, Blythe P.
Yap, Stanley A.
Ghosh, Paramita M.
deVere White, Ralph W.
author_facet Vinall, Ruth L.
Tepper, Clifford G.
Ripoll, Alexandra A. Z.
Gandour-Edwards, Regina F.
Durbin-Johnson, Blythe P.
Yap, Stanley A.
Ghosh, Paramita M.
deVere White, Ralph W.
author_sort Vinall, Ruth L.
collection PubMed
description The identification and development of biomarkers which predict response of muscle invasive bladder cancer (MIBC) patients to neoadjuvant chemotherapy would likely increase usage of this treatment option and thereby improve patient survival rates. MiRNA array and qRT-PCR validation was used to identify miRNA which are associated with response to neoadjuvant chemotherapy. RNA was extracted from a total of 41 archival, fully annotated, MIBC patient diagnostic biopsies (20 chemo-responders and 21 non-responders (response is defined as > 5 year survival rate and being pT0 post-chemotherapy)). Microarray and qPCR identified let-7c as being differentially expressed in chemo-responder versus non-responder patients. Patients with higher let-7c expression levels had significantly higher odds of responding to chemotherapy (p = 0.023, OR 2.493, 95% CI 1.121, 5.546), and assessment of let-7c levels allowed for prediction of patient response (AUC 0.72, positive predictive value 59%). Decreased let-7c was associated with MIBC incidence (p < 0.001), and significantly correlated with other related miRNA including those that were not differentially expressed between responders and non-responders. The combined data indicate let-7c plays a role in mediating chemoresistance to neoadjuvant chemotherapy in MIBC patients, and is a modest, yet clinically meaningful, predictor of patient response.
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spelling pubmed-49189472016-07-05 Decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy Vinall, Ruth L. Tepper, Clifford G. Ripoll, Alexandra A. Z. Gandour-Edwards, Regina F. Durbin-Johnson, Blythe P. Yap, Stanley A. Ghosh, Paramita M. deVere White, Ralph W. Genes Cancer Research Paper The identification and development of biomarkers which predict response of muscle invasive bladder cancer (MIBC) patients to neoadjuvant chemotherapy would likely increase usage of this treatment option and thereby improve patient survival rates. MiRNA array and qRT-PCR validation was used to identify miRNA which are associated with response to neoadjuvant chemotherapy. RNA was extracted from a total of 41 archival, fully annotated, MIBC patient diagnostic biopsies (20 chemo-responders and 21 non-responders (response is defined as > 5 year survival rate and being pT0 post-chemotherapy)). Microarray and qPCR identified let-7c as being differentially expressed in chemo-responder versus non-responder patients. Patients with higher let-7c expression levels had significantly higher odds of responding to chemotherapy (p = 0.023, OR 2.493, 95% CI 1.121, 5.546), and assessment of let-7c levels allowed for prediction of patient response (AUC 0.72, positive predictive value 59%). Decreased let-7c was associated with MIBC incidence (p < 0.001), and significantly correlated with other related miRNA including those that were not differentially expressed between responders and non-responders. The combined data indicate let-7c plays a role in mediating chemoresistance to neoadjuvant chemotherapy in MIBC patients, and is a modest, yet clinically meaningful, predictor of patient response. Impact Journals LLC 2016-03 /pmc/articles/PMC4918947/ /pubmed/27382433 http://dx.doi.org/10.18632/genesandcancer.103 Text en Copyright: © 2016 Vinall et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Vinall, Ruth L.
Tepper, Clifford G.
Ripoll, Alexandra A. Z.
Gandour-Edwards, Regina F.
Durbin-Johnson, Blythe P.
Yap, Stanley A.
Ghosh, Paramita M.
deVere White, Ralph W.
Decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy
title Decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy
title_full Decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy
title_fullStr Decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy
title_full_unstemmed Decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy
title_short Decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy
title_sort decreased expression of let-7c is associated with non-response of muscle-invasive bladder cancer patients to neoadjuvant chemotherapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918947/
https://www.ncbi.nlm.nih.gov/pubmed/27382433
http://dx.doi.org/10.18632/genesandcancer.103
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