Cargando…
Repositioning CEP-1347, a chemical agent originally developed for the treatment of Parkinson’s disease, as an anti-cancer stem cell drug
CEP-1347 is a mixed lineage kinase inhibitor tested in a large-scale phase 2/3 clinical trial in early Parkinson’s disease, in which its safety and tolerability, but nevertheless not efficacy, was demonstrated. Here we identify by drug repositioning CEP-1347 as a potential anti-cancer stem cell drug...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706919/ https://www.ncbi.nlm.nih.gov/pubmed/29212273 http://dx.doi.org/10.18632/oncotarget.22033 |
_version_ | 1783282316074811392 |
---|---|
author | Okada, Masashi Takeda, Hiroyuki Sakaki, Hirotsugu Kuramoto, Kenta Suzuki, Shuhei Sanomachi, Tomomi Togashi, Keita Seino, Shizuka Kitanaka, Chifumi |
author_facet | Okada, Masashi Takeda, Hiroyuki Sakaki, Hirotsugu Kuramoto, Kenta Suzuki, Shuhei Sanomachi, Tomomi Togashi, Keita Seino, Shizuka Kitanaka, Chifumi |
author_sort | Okada, Masashi |
collection | PubMed |
description | CEP-1347 is a mixed lineage kinase inhibitor tested in a large-scale phase 2/3 clinical trial in early Parkinson’s disease, in which its safety and tolerability, but nevertheless not efficacy, was demonstrated. Here we identify by drug repositioning CEP-1347 as a potential anti-cancer stem cell drug. In vitro, CEP-1347 efficiently induced differentiation and inhibited the self-renewal and tumor-initiating capacities of human cancer stem cells from glioblastoma as well as from pancreatic and ovarian cancers at clinically-relevant concentrations, without impairing the viability of normal fibroblasts and neural stem cells. In vivo, a 10-day systemic administration of CEP-1347 at a dose that was less than 1/10 the mouse equivalent of the dose safely given to humans for 2 years was sufficient to effectively reduce tumor-initiating cancer stem cells within established tumors in mice. Furthermore, the same treatment protocol significantly extended the survival of mice receiving orthotopic implantation of glioma stem cells. Together, our findings suggest that CEP-1347 is a promising candidate for cancer stem cell-targeting therapy and that further clinical and preclinical studies are warranted to evaluate its efficacy in cancer treatment. |
format | Online Article Text |
id | pubmed-5706919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57069192017-12-05 Repositioning CEP-1347, a chemical agent originally developed for the treatment of Parkinson’s disease, as an anti-cancer stem cell drug Okada, Masashi Takeda, Hiroyuki Sakaki, Hirotsugu Kuramoto, Kenta Suzuki, Shuhei Sanomachi, Tomomi Togashi, Keita Seino, Shizuka Kitanaka, Chifumi Oncotarget Research Paper CEP-1347 is a mixed lineage kinase inhibitor tested in a large-scale phase 2/3 clinical trial in early Parkinson’s disease, in which its safety and tolerability, but nevertheless not efficacy, was demonstrated. Here we identify by drug repositioning CEP-1347 as a potential anti-cancer stem cell drug. In vitro, CEP-1347 efficiently induced differentiation and inhibited the self-renewal and tumor-initiating capacities of human cancer stem cells from glioblastoma as well as from pancreatic and ovarian cancers at clinically-relevant concentrations, without impairing the viability of normal fibroblasts and neural stem cells. In vivo, a 10-day systemic administration of CEP-1347 at a dose that was less than 1/10 the mouse equivalent of the dose safely given to humans for 2 years was sufficient to effectively reduce tumor-initiating cancer stem cells within established tumors in mice. Furthermore, the same treatment protocol significantly extended the survival of mice receiving orthotopic implantation of glioma stem cells. Together, our findings suggest that CEP-1347 is a promising candidate for cancer stem cell-targeting therapy and that further clinical and preclinical studies are warranted to evaluate its efficacy in cancer treatment. Impact Journals LLC 2017-10-24 /pmc/articles/PMC5706919/ /pubmed/29212273 http://dx.doi.org/10.18632/oncotarget.22033 Text en Copyright: © 2017 Okada et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Okada, Masashi Takeda, Hiroyuki Sakaki, Hirotsugu Kuramoto, Kenta Suzuki, Shuhei Sanomachi, Tomomi Togashi, Keita Seino, Shizuka Kitanaka, Chifumi Repositioning CEP-1347, a chemical agent originally developed for the treatment of Parkinson’s disease, as an anti-cancer stem cell drug |
title | Repositioning CEP-1347, a chemical agent originally developed for the treatment of Parkinson’s disease, as an anti-cancer stem cell drug |
title_full | Repositioning CEP-1347, a chemical agent originally developed for the treatment of Parkinson’s disease, as an anti-cancer stem cell drug |
title_fullStr | Repositioning CEP-1347, a chemical agent originally developed for the treatment of Parkinson’s disease, as an anti-cancer stem cell drug |
title_full_unstemmed | Repositioning CEP-1347, a chemical agent originally developed for the treatment of Parkinson’s disease, as an anti-cancer stem cell drug |
title_short | Repositioning CEP-1347, a chemical agent originally developed for the treatment of Parkinson’s disease, as an anti-cancer stem cell drug |
title_sort | repositioning cep-1347, a chemical agent originally developed for the treatment of parkinson’s disease, as an anti-cancer stem cell drug |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706919/ https://www.ncbi.nlm.nih.gov/pubmed/29212273 http://dx.doi.org/10.18632/oncotarget.22033 |
work_keys_str_mv | AT okadamasashi repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug AT takedahiroyuki repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug AT sakakihirotsugu repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug AT kuramotokenta repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug AT suzukishuhei repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug AT sanomachitomomi repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug AT togashikeita repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug AT seinoshizuka repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug AT kitanakachifumi repositioningcep1347achemicalagentoriginallydevelopedforthetreatmentofparkinsonsdiseaseasananticancerstemcelldrug |