TY - JOUR
T1 - Maiden voyage
T2 - induced pluripotent stem cell-based drug screening for amyotrophic lateral sclerosis
AU - Ito, Daisuke
AU - Morimoto, Satoru
AU - Takahashi, Shinichi
AU - Okada, Kensuke
AU - Nakahara, Jin
AU - Okano, Hideyuki
N1 - Funding Information:
D.I. has received funding for speaker honoraria from Mitsubishi Tanabe and is supported by the Ministry of Education, Culture, Sports, Science and Technology of Japan (No. 21H02812), the Foundation of Japan Amyotrophic Lateral Sclerosis Association, the Ice Bucket Challenge Grant (Japan Amyotrophic Lateral Sclerosis Association), and the Serika Fund. J.N. reports grants from Japan Agency for Medical Research and Development (AMED), grants from K Pharma Inc, and non-financial support from GSK during the conduct of the study. H.O. reports grants and personal fees from K Pharma Inc. during the conduct of the study; personal fees from SanBio Co. Ltd.; and personal fees from Regenerative Medicine iPS Gateway Centre Co., Ltd., outside the submitted work. In addition, he has a patent therapeutic agent for amyotrophic lateral sclerosis and composition for treatment licensed to K Pharma Inc. and grant support from AMED [The Acceleration Program for Intractable Disease Research Utilizing Disease-specific iPS Cells (grant numbers JP 19bm0804003, JP 20bm0804003, JP 21bm0804003) and Research on Practical Application of Innovative Pharmaceutical and Medical Devices for Rare and Intractable Diseases (grant numbers JP 18ek0109395, JP 19ek0109395, JP 20ek0109395, JP 18ek0109329, JP 19ek0109329, JP 20ek0109329)].
Funding Information:
D.I. has received funding for speaker honoraria from Mitsubishi Tanabe and is supported by the Ministry of Education, Culture, Sports, Science and Technology of Japan (No. 21H02812), the Foundation of Japan Amyotrophic Lateral Sclerosis Association, the Ice Bucket Challenge Grant (Japan Amyotrophic Lateral Sclerosis Association), and the Serika Fund. J.N. reports grants from Japan Agency for Medical Research and Development (AMED), grants from K Pharma Inc, and non-financial support from GSK during the conduct of the study. H.O. reports grants and personal fees from K Pharma Inc. during the conduct of the study; personal fees from SanBio Co. Ltd.; and personal fees from Regenerative Medicine iPS Gateway Centre Co., Ltd., outside the submitted work. In addition, he has a patent therapeutic agent for amyotrophic lateral sclerosis and composition for treatment licensed to K Pharma Inc. and grant support from AMED [The Acceleration Program for Intractable Disease Research Utilizing Disease-specific iPS Cells (grant numbers JP 19bm0804003, JP 20bm0804003, JP 21bm0804003) and Research on Practical Application of Innovative Pharmaceutical and Medical Devices for Rare and Intractable Diseases (grant numbers JP 18ek0109395, JP 19ek0109395, JP 20ek0109395, JP 18ek0109329, JP 19ek0109329, JP 20ek0109329)].
Publisher Copyright:
© The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Using patient-derived induced pluripotent stem cells, neurodegenerative disease phenotypes have been recapitulated and their pathogenesis analysed leading to significant progress in drug screening. In amyotrophic lateral sclerosis, high-throughput screening using induced pluripotent stem cells-derived motor neurons has identified candidate drugs. Owing to induced pluripotent stem cell-based drug evaluation/screening, three compounds, retigabine, ropinirole and bosutinib, have progressed to clinical trials. Retigabine blocks hyperexcitability and improves survival in amyotrophic lateral sclerosis patient-derived motor neurons. In a randomized clinical trial (n = 65), treatment with retigabine reduced neuronal excitability after 8 weeks. Ropinirole, identified in a high-throughput screening, attenuates pathological phenotypes in patient-derived motor neurons. In a trial limited by a small sample size (n = 20), ropinirole was tolerable and had clinical benefits on function and survival. A phase 1 study of bosutinib has reported safety and tolerability for 12 weeks. Thus, these clinical trials show safety and positive effects and confirm the reliability of stem cell-based drug discovery. This novel strategy leads to reduced costs and time when compared to animal testing and opens new avenues for therapy in intractable diseases.
AB - Using patient-derived induced pluripotent stem cells, neurodegenerative disease phenotypes have been recapitulated and their pathogenesis analysed leading to significant progress in drug screening. In amyotrophic lateral sclerosis, high-throughput screening using induced pluripotent stem cells-derived motor neurons has identified candidate drugs. Owing to induced pluripotent stem cell-based drug evaluation/screening, three compounds, retigabine, ropinirole and bosutinib, have progressed to clinical trials. Retigabine blocks hyperexcitability and improves survival in amyotrophic lateral sclerosis patient-derived motor neurons. In a randomized clinical trial (n = 65), treatment with retigabine reduced neuronal excitability after 8 weeks. Ropinirole, identified in a high-throughput screening, attenuates pathological phenotypes in patient-derived motor neurons. In a trial limited by a small sample size (n = 20), ropinirole was tolerable and had clinical benefits on function and survival. A phase 1 study of bosutinib has reported safety and tolerability for 12 weeks. Thus, these clinical trials show safety and positive effects and confirm the reliability of stem cell-based drug discovery. This novel strategy leads to reduced costs and time when compared to animal testing and opens new avenues for therapy in intractable diseases.
KW - amyotrophic lateral sclerosis
KW - bosutinib
KW - drug screening
KW - induced pluripotent stem cells
KW - retigabine
KW - ropinirole
UR - http://www.scopus.com/inward/record.url?scp=85141777634&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85141777634&partnerID=8YFLogxK
U2 - 10.1093/brain/awac306
DO - 10.1093/brain/awac306
M3 - Review article
C2 - 36004509
AN - SCOPUS:85141777634
SN - 0006-8950
VL - 146
SP - 13
EP - 19
JO - Brain
JF - Brain
IS - 1
ER -