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Key MicroRNA’s and Their Targetome in Adrenocortical Cancer

Adrenocortical Carcinoma (ACC) is a rare but aggressive malignancy with poor prognosis and limited response to available systemic therapies. Although complete surgical resection gives the best chance for long-term survival, ACC has a two-year recurrence rate of 50%, which poses a therapeutic challen...

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Autores principales: Chehade, Marthe, Bullock, Martyn, Glover, Anthony, Hutvagner, Gyorgy, Sidhu, Stan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465134/
https://www.ncbi.nlm.nih.gov/pubmed/32781574
http://dx.doi.org/10.3390/cancers12082198
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author Chehade, Marthe
Bullock, Martyn
Glover, Anthony
Hutvagner, Gyorgy
Sidhu, Stan
author_facet Chehade, Marthe
Bullock, Martyn
Glover, Anthony
Hutvagner, Gyorgy
Sidhu, Stan
author_sort Chehade, Marthe
collection PubMed
description Adrenocortical Carcinoma (ACC) is a rare but aggressive malignancy with poor prognosis and limited response to available systemic therapies. Although complete surgical resection gives the best chance for long-term survival, ACC has a two-year recurrence rate of 50%, which poses a therapeutic challenge. High throughput analyses focused on characterizing the molecular signature of ACC have revealed specific micro-RNAs (miRNAs) that are associated with aggressive tumor phenotypes. MiRNAs are small non-coding RNA molecules that regulate gene expression by inhibiting mRNA translation or degrading mRNA transcripts and have been generally implicated in carcinogenesis. This review summarizes the current insights into dysregulated miRNAs in ACC tumorigenesis, their known functions, and specific targetomes. In addition, we explore the possibility of particular miRNAs to be exploited as clinical biomarkers in ACC and as potential therapeutics.
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spelling pubmed-74651342020-09-04 Key MicroRNA’s and Their Targetome in Adrenocortical Cancer Chehade, Marthe Bullock, Martyn Glover, Anthony Hutvagner, Gyorgy Sidhu, Stan Cancers (Basel) Review Adrenocortical Carcinoma (ACC) is a rare but aggressive malignancy with poor prognosis and limited response to available systemic therapies. Although complete surgical resection gives the best chance for long-term survival, ACC has a two-year recurrence rate of 50%, which poses a therapeutic challenge. High throughput analyses focused on characterizing the molecular signature of ACC have revealed specific micro-RNAs (miRNAs) that are associated with aggressive tumor phenotypes. MiRNAs are small non-coding RNA molecules that regulate gene expression by inhibiting mRNA translation or degrading mRNA transcripts and have been generally implicated in carcinogenesis. This review summarizes the current insights into dysregulated miRNAs in ACC tumorigenesis, their known functions, and specific targetomes. In addition, we explore the possibility of particular miRNAs to be exploited as clinical biomarkers in ACC and as potential therapeutics. MDPI 2020-08-06 /pmc/articles/PMC7465134/ /pubmed/32781574 http://dx.doi.org/10.3390/cancers12082198 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chehade, Marthe
Bullock, Martyn
Glover, Anthony
Hutvagner, Gyorgy
Sidhu, Stan
Key MicroRNA’s and Their Targetome in Adrenocortical Cancer
title Key MicroRNA’s and Their Targetome in Adrenocortical Cancer
title_full Key MicroRNA’s and Their Targetome in Adrenocortical Cancer
title_fullStr Key MicroRNA’s and Their Targetome in Adrenocortical Cancer
title_full_unstemmed Key MicroRNA’s and Their Targetome in Adrenocortical Cancer
title_short Key MicroRNA’s and Their Targetome in Adrenocortical Cancer
title_sort key microrna’s and their targetome in adrenocortical cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465134/
https://www.ncbi.nlm.nih.gov/pubmed/32781574
http://dx.doi.org/10.3390/cancers12082198
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