Class I and II Histone Deacetylase Inhibitor LBH589 Promotes Endocrine Differentiation in Bone Marrow Derived Human Mesenchymal Stem Cells and Suppresses Uncontrolled Proliferation.
Bone Marrow Cells
/ drug effects
Carcinogenesis
/ drug effects
Cell Differentiation
/ drug effects
Cell Proliferation
/ drug effects
Histone Deacetylase Inhibitors
/ pharmacology
Humans
Islets of Langerhans
/ drug effects
Mesenchymal Stem Cell Transplantation
Mesenchymal Stem Cells
/ drug effects
Panobinostat
/ pharmacology
Journal
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association
ISSN: 1439-3646
Titre abrégé: Exp Clin Endocrinol Diabetes
Pays: Germany
ID NLM: 9505926
Informations de publication
Date de publication:
May 2021
May 2021
Historique:
pubmed:
14
2
2020
medline:
25
11
2021
entrez:
14
2
2020
Statut:
ppublish
Résumé
Mesenchymal stem cells are useful tools employed in clinical and preclinical medicine. Their beneficial potential in especially degenerative as well as autoimmune diseases is a constant focus of research. Regarding diabetes mellitus, transplantation of stem cells is seen as a possible therapeutic approach to overcome the loss of endocrine pancreatic cells. It was reported that co-transplantation of mesenchymal stem cells with pancreatic islet cells improves function and survival of the graft. However, these multipotent progenitors may be able to form tumors, especially under immunosuppressed conditions. Histone deacetylase inhibitors might offer the potential to overcome this issue. These small molecules can induce cell differentiation and control proliferation. Their potential to control lineage development of stem cells has been distinctly demonstrated in the treatment of cancer, mainly in hematopoietic neoplasias.In this study, we demonstrate that human bone marrow-derived mesenchymal stem cells exhibit low carcinogenic potential in an immunosuppressed condition
Substances chimiques
Histone Deacetylase Inhibitors
0
Panobinostat
9647FM7Y3Z
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
357-364Informations de copyright
Thieme. All rights reserved.
Déclaration de conflit d'intérêts
The authors declare that they have no conflict of interest.