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MicroRNAs and Their Targetomes in Tumor-Immune Communication

The development of cancer is a complex and dynamically regulated multiple-step process that involves many changes in gene expression. Over the last decade, microRNAs (miRNAs), a class of short regulatory non-coding RNAs, have emerged as key molecular effectors and regulators of tumorigenesis. While...

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Detalles Bibliográficos
Autores principales: Cho, Sunglim, Tai, Jesse W., Lu, Li-Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465095/
https://www.ncbi.nlm.nih.gov/pubmed/32722019
http://dx.doi.org/10.3390/cancers12082025
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author Cho, Sunglim
Tai, Jesse W.
Lu, Li-Fan
author_facet Cho, Sunglim
Tai, Jesse W.
Lu, Li-Fan
author_sort Cho, Sunglim
collection PubMed
description The development of cancer is a complex and dynamically regulated multiple-step process that involves many changes in gene expression. Over the last decade, microRNAs (miRNAs), a class of short regulatory non-coding RNAs, have emerged as key molecular effectors and regulators of tumorigenesis. While aberrant expression of miRNAs or dysregulated miRNA-mediated gene regulation in tumor cells have been shown to be capable of directly promoting or inhibiting tumorigenesis, considering the well-reported role of the immune system in cancer, tumor-derived miRNAs could also impact tumor growth through regulating anti-tumor immune responses. Here, we discuss howmiRNAs can function as central mediators that influence the crosstalk between cancer and the immune system. Moreover, we also review the current progress in the development of novel experimental approaches for miRNA target identification that will facilitate our understanding of miRNA-mediated gene regulation in not only human malignancies, but also in other genetic disorders.
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spelling pubmed-74650952020-09-04 MicroRNAs and Their Targetomes in Tumor-Immune Communication Cho, Sunglim Tai, Jesse W. Lu, Li-Fan Cancers (Basel) Perspective The development of cancer is a complex and dynamically regulated multiple-step process that involves many changes in gene expression. Over the last decade, microRNAs (miRNAs), a class of short regulatory non-coding RNAs, have emerged as key molecular effectors and regulators of tumorigenesis. While aberrant expression of miRNAs or dysregulated miRNA-mediated gene regulation in tumor cells have been shown to be capable of directly promoting or inhibiting tumorigenesis, considering the well-reported role of the immune system in cancer, tumor-derived miRNAs could also impact tumor growth through regulating anti-tumor immune responses. Here, we discuss howmiRNAs can function as central mediators that influence the crosstalk between cancer and the immune system. Moreover, we also review the current progress in the development of novel experimental approaches for miRNA target identification that will facilitate our understanding of miRNA-mediated gene regulation in not only human malignancies, but also in other genetic disorders. MDPI 2020-07-24 /pmc/articles/PMC7465095/ /pubmed/32722019 http://dx.doi.org/10.3390/cancers12082025 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 Perspective
Cho, Sunglim
Tai, Jesse W.
Lu, Li-Fan
MicroRNAs and Their Targetomes in Tumor-Immune Communication
title MicroRNAs and Their Targetomes in Tumor-Immune Communication
title_full MicroRNAs and Their Targetomes in Tumor-Immune Communication
title_fullStr MicroRNAs and Their Targetomes in Tumor-Immune Communication
title_full_unstemmed MicroRNAs and Their Targetomes in Tumor-Immune Communication
title_short MicroRNAs and Their Targetomes in Tumor-Immune Communication
title_sort micrornas and their targetomes in tumor-immune communication
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465095/
https://www.ncbi.nlm.nih.gov/pubmed/32722019
http://dx.doi.org/10.3390/cancers12082025
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