Cargando…

Inhibiting the NLRP3 Inflammasome With Methylene Blue as Treatment Adjunct in Myelodysplasia

Myelodysplasia refers to a group of clonal hematopoietic neoplasms characterized by genetic heterogeneity, different clinical behaviors and prognoses. Some of this group of bone marrow failure conditions have known external causes, some are of unknown origin. Within marrow, intracellular, and extrac...

Descripción completa

Detalles Bibliográficos
Autor principal: Kast, Richard E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072867/
https://www.ncbi.nlm.nih.gov/pubmed/30101125
http://dx.doi.org/10.3389/fonc.2018.00280
_version_ 1783344075688116224
author Kast, Richard E.
author_facet Kast, Richard E.
author_sort Kast, Richard E.
collection PubMed
description Myelodysplasia refers to a group of clonal hematopoietic neoplasms characterized by genetic heterogeneity, different clinical behaviors and prognoses. Some of this group of bone marrow failure conditions have known external causes, some are of unknown origin. Within marrow, intracellular, and extracellular elements of the innate immune system are activated and contribute to creation of multiple cytogenetic abnormalities and are central to the mode of hematopoietic cell failure. Basiorka et al. showed that NLRP3 inflammasome activity is essential to the innate immune system's destruction of marrow hematopoietic cells commonly in myelodysplasia. In April 2018 Hao et al. reported that methylene blue inhibits rat NLRP3 inflammasome function. Methylene blue has been in continuous use in humans for over a century. It is associated with an eminently benign side effect profile in human use. If as in rodents, methylene blue also inhibits NLRP3 inflammasome function in human myelodysplasia a trial of adjunctive methylene blue treatment in transfusion dependent, low risk myelodysplasia where marrow inflammation and apoptosis predominates, would be worth trying. HIGHLIGHTS: - Cytogenetic abnormalities and innate immune activation are seen in myelodysplasia; - The NLRP3 inflammasome is a core element generating marrow failure of myelodysplasia; - In April 2018 methylene blue was reported to potently inhibit NLRP3 inflammasome function; - Methylene blue has benign side effects and has been in human use for a century; - Study of methylene blue treatment of myelodysplasia would be a low-risk intervention;
format Online
Article
Text
id pubmed-6072867
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-60728672018-08-10 Inhibiting the NLRP3 Inflammasome With Methylene Blue as Treatment Adjunct in Myelodysplasia Kast, Richard E. Front Oncol Oncology Myelodysplasia refers to a group of clonal hematopoietic neoplasms characterized by genetic heterogeneity, different clinical behaviors and prognoses. Some of this group of bone marrow failure conditions have known external causes, some are of unknown origin. Within marrow, intracellular, and extracellular elements of the innate immune system are activated and contribute to creation of multiple cytogenetic abnormalities and are central to the mode of hematopoietic cell failure. Basiorka et al. showed that NLRP3 inflammasome activity is essential to the innate immune system's destruction of marrow hematopoietic cells commonly in myelodysplasia. In April 2018 Hao et al. reported that methylene blue inhibits rat NLRP3 inflammasome function. Methylene blue has been in continuous use in humans for over a century. It is associated with an eminently benign side effect profile in human use. If as in rodents, methylene blue also inhibits NLRP3 inflammasome function in human myelodysplasia a trial of adjunctive methylene blue treatment in transfusion dependent, low risk myelodysplasia where marrow inflammation and apoptosis predominates, would be worth trying. HIGHLIGHTS: - Cytogenetic abnormalities and innate immune activation are seen in myelodysplasia; - The NLRP3 inflammasome is a core element generating marrow failure of myelodysplasia; - In April 2018 methylene blue was reported to potently inhibit NLRP3 inflammasome function; - Methylene blue has benign side effects and has been in human use for a century; - Study of methylene blue treatment of myelodysplasia would be a low-risk intervention; Frontiers Media S.A. 2018-07-27 /pmc/articles/PMC6072867/ /pubmed/30101125 http://dx.doi.org/10.3389/fonc.2018.00280 Text en Copyright © 2018 Kast. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Kast, Richard E.
Inhibiting the NLRP3 Inflammasome With Methylene Blue as Treatment Adjunct in Myelodysplasia
title Inhibiting the NLRP3 Inflammasome With Methylene Blue as Treatment Adjunct in Myelodysplasia
title_full Inhibiting the NLRP3 Inflammasome With Methylene Blue as Treatment Adjunct in Myelodysplasia
title_fullStr Inhibiting the NLRP3 Inflammasome With Methylene Blue as Treatment Adjunct in Myelodysplasia
title_full_unstemmed Inhibiting the NLRP3 Inflammasome With Methylene Blue as Treatment Adjunct in Myelodysplasia
title_short Inhibiting the NLRP3 Inflammasome With Methylene Blue as Treatment Adjunct in Myelodysplasia
title_sort inhibiting the nlrp3 inflammasome with methylene blue as treatment adjunct in myelodysplasia
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072867/
https://www.ncbi.nlm.nih.gov/pubmed/30101125
http://dx.doi.org/10.3389/fonc.2018.00280
work_keys_str_mv AT kastricharde inhibitingthenlrp3inflammasomewithmethyleneblueastreatmentadjunctinmyelodysplasia