Cargando…

MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies

The initial response of lymphoid malignancies to glucocorticoids (GCs) is a critical parameter predicting successful treatment. Although being known as a strong inducer of apoptosis in lymphoid cells for almost a century, the signaling pathways regulating the susceptibility of the cells to GCs are o...

Descripción completa

Detalles Bibliográficos
Autor principal: Sionov, Ronit Vogt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569899/
https://www.ncbi.nlm.nih.gov/pubmed/23431463
http://dx.doi.org/10.1155/2013/348212
_version_ 1782258983497629696
author Sionov, Ronit Vogt
author_facet Sionov, Ronit Vogt
author_sort Sionov, Ronit Vogt
collection PubMed
description The initial response of lymphoid malignancies to glucocorticoids (GCs) is a critical parameter predicting successful treatment. Although being known as a strong inducer of apoptosis in lymphoid cells for almost a century, the signaling pathways regulating the susceptibility of the cells to GCs are only partly revealed. There is still a need to develop clinical tests that can predict the outcome of GC therapy. In this paper, I discuss important parameters modulating the pro-apoptotic effects of GCs, with a specific emphasis on the microRNA world comprised of small players with big impacts. The journey through the multifaceted complexity of GC-induced apoptosis brings forth explanations for the differential treatment response and raises potential strategies for overcoming drug resistance.
format Online
Article
Text
id pubmed-3569899
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-35698992013-02-21 MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies Sionov, Ronit Vogt ISRN Hematol Review Article The initial response of lymphoid malignancies to glucocorticoids (GCs) is a critical parameter predicting successful treatment. Although being known as a strong inducer of apoptosis in lymphoid cells for almost a century, the signaling pathways regulating the susceptibility of the cells to GCs are only partly revealed. There is still a need to develop clinical tests that can predict the outcome of GC therapy. In this paper, I discuss important parameters modulating the pro-apoptotic effects of GCs, with a specific emphasis on the microRNA world comprised of small players with big impacts. The journey through the multifaceted complexity of GC-induced apoptosis brings forth explanations for the differential treatment response and raises potential strategies for overcoming drug resistance. Hindawi Publishing Corporation 2013-01-29 /pmc/articles/PMC3569899/ /pubmed/23431463 http://dx.doi.org/10.1155/2013/348212 Text en Copyright © 2013 Ronit Vogt Sionov. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Sionov, Ronit Vogt
MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies
title MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies
title_full MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies
title_fullStr MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies
title_full_unstemmed MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies
title_short MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies
title_sort micrornas and glucocorticoid-induced apoptosis in lymphoid malignancies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569899/
https://www.ncbi.nlm.nih.gov/pubmed/23431463
http://dx.doi.org/10.1155/2013/348212
work_keys_str_mv AT sionovronitvogt micrornasandglucocorticoidinducedapoptosisinlymphoidmalignancies