Cargando…

Mechanism of T cell regulation by microRNAs

MicroRNAs (miRNAs) are small, non-coding single-stranded RNAs that can modulate target gene expression at post-transcriptional level and participate in cell proliferation, differentiation, and apoptosis. T cells have important functions in acquired immune response; miRNAs regulate this immune respon...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Juan, Wu, Chang-Ping, Lu, Bin-Feng, Jiang, Jing-Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Anti-Cancer Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860337/
https://www.ncbi.nlm.nih.gov/pubmed/24379987
http://dx.doi.org/10.7497/j.issn.2095-3941.2013.03.002
_version_ 1782295524173414400
author Liu, Juan
Wu, Chang-Ping
Lu, Bin-Feng
Jiang, Jing-Ting
author_facet Liu, Juan
Wu, Chang-Ping
Lu, Bin-Feng
Jiang, Jing-Ting
author_sort Liu, Juan
collection PubMed
description MicroRNAs (miRNAs) are small, non-coding single-stranded RNAs that can modulate target gene expression at post-transcriptional level and participate in cell proliferation, differentiation, and apoptosis. T cells have important functions in acquired immune response; miRNAs regulate this immune response by targeting the mRNAs of genes involved in T cell development, proliferation, differentiation, and function. For instance, miR-181 family members function in progression by targeting Bcl2 and CD69, among others. MiR-17 to miR-92 clusters function by binding to CREB1, PTEN, and Bim. Considering that the suppression of T cell-mediated immune responses against tumor cells is involved in cancer progression, we should investigate the mechanism by which miRNA regulates T cells to develop new approaches for cancer treatment.
format Online
Article
Text
id pubmed-3860337
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Chinese Anti-Cancer Association
record_format MEDLINE/PubMed
spelling pubmed-38603372013-12-30 Mechanism of T cell regulation by microRNAs Liu, Juan Wu, Chang-Ping Lu, Bin-Feng Jiang, Jing-Ting Cancer Biol Med Review MicroRNAs (miRNAs) are small, non-coding single-stranded RNAs that can modulate target gene expression at post-transcriptional level and participate in cell proliferation, differentiation, and apoptosis. T cells have important functions in acquired immune response; miRNAs regulate this immune response by targeting the mRNAs of genes involved in T cell development, proliferation, differentiation, and function. For instance, miR-181 family members function in progression by targeting Bcl2 and CD69, among others. MiR-17 to miR-92 clusters function by binding to CREB1, PTEN, and Bim. Considering that the suppression of T cell-mediated immune responses against tumor cells is involved in cancer progression, we should investigate the mechanism by which miRNA regulates T cells to develop new approaches for cancer treatment. Chinese Anti-Cancer Association 2013-09 /pmc/articles/PMC3860337/ /pubmed/24379987 http://dx.doi.org/10.7497/j.issn.2095-3941.2013.03.002 Text en 2013 Cancer Biology & Medicine This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Review
Liu, Juan
Wu, Chang-Ping
Lu, Bin-Feng
Jiang, Jing-Ting
Mechanism of T cell regulation by microRNAs
title Mechanism of T cell regulation by microRNAs
title_full Mechanism of T cell regulation by microRNAs
title_fullStr Mechanism of T cell regulation by microRNAs
title_full_unstemmed Mechanism of T cell regulation by microRNAs
title_short Mechanism of T cell regulation by microRNAs
title_sort mechanism of t cell regulation by micrornas
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860337/
https://www.ncbi.nlm.nih.gov/pubmed/24379987
http://dx.doi.org/10.7497/j.issn.2095-3941.2013.03.002
work_keys_str_mv AT liujuan mechanismoftcellregulationbymicrornas
AT wuchangping mechanismoftcellregulationbymicrornas
AT lubinfeng mechanismoftcellregulationbymicrornas
AT jiangjingting mechanismoftcellregulationbymicrornas