Pharmacologic characterization of TBP1901, a prodrug form of aglycone curcumin, and CRISPR-Cas9 screen for therapeutic targets of aglycone curcumin.


Journal

European journal of pharmacology
ISSN: 1879-0712
Titre abrégé: Eur J Pharmacol
Pays: Netherlands
ID NLM: 1254354

Informations de publication

Date de publication:
15 Nov 2022
Historique:
received: 25 04 2022
revised: 04 10 2022
accepted: 05 10 2022
pubmed: 14 10 2022
medline: 9 11 2022
entrez: 13 10 2022
Statut: ppublish

Résumé

Curcumin (aglycone curcumin) has antitumor properties in a variety of malignancies via the alteration of multiple cancer-related biological pathways; however, its clinical application has been hampered due to its poor bioavailability. To overcome this limitation, we have developed a synthesized curcumin β-D-glucuronide sodium salt (TBP1901), a prodrug form of aglycone curcumin. In this study, we aimed to clarify the pharmacologic characteristics of TBP1901. In β-glucuronidase (GUSB)-proficient mice, both curcumin β-D-glucuronide and its active metabolite, aglycone curcumin, were detected in the blood after TBP1901 injection, whereas only curcumin β-D-glucuronide was detected in GUSB-impaired mice, suggesting that GUSB plays a pivotal role in the conversion of TBP1901 into aglycone curcumin in vivo. TBP1901 itself had minimal antitumor effects in vitro, whereas it demonstrated significant antitumor effects in vivo. Genome-wide clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 screen disclosed the genes associated with NF-κB signaling pathway and mitochondria were among the highest hit. In vitro, aglycone curcumin inhibited NF-kappa B signaling pathways whereas it caused production of reactive oxygen species (ROS). ROS scavenger, N-acetyl-L-cysteine, partially reversed antitumor effects of aglycone curcumin. In summary, TBP1901 can exert antitumor effects as a prodrug of aglycone curcumin through GUSB-dependent activation.

Identifiants

pubmed: 36228744
pii: S0014-2999(22)00582-9
doi: 10.1016/j.ejphar.2022.175321
pii:
doi:

Substances chimiques

Curcumin IT942ZTH98
Glucuronidase EC 3.2.1.31
Glucuronides 0
NF-kappa B 0
Prodrugs 0
Reactive Oxygen Species 0
TBP1901 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

175321

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Tadashi Hashimoto is the chief executive officer of Therabiopharma Inc. Atushi Imaizumi is the senior vice president of Therabiopharma Inc. Tomoyuki Abe, Hitomi Ozawa-Umeta, Atsuhiro Kishimoto, and Yasuhiro Katsuura are employees of Therabiopharma Inc. Masashi Kanai. and Hideaki Kakeya own equity and they are the scientific consultants of Therabiopharma Inc.

Auteurs

Tomoyuki Abe (T)

Therabiopharma Inc., Kanagawa, Japan.

Yoshihito Horisawa (Y)

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Osamu Kikuchi (O)

Department of Therapeutic Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Hitomi Ozawa-Umeta (H)

Therabiopharma Inc., Kanagawa, Japan.

Atsuhiro Kishimoto (A)

Therabiopharma Inc., Kanagawa, Japan.

Yasuhiro Katsuura (Y)

Therabiopharma Inc., Kanagawa, Japan.

Atsushi Imaizumi (A)

Therabiopharma Inc., Kanagawa, Japan.

Tadashi Hashimoto (T)

Therabiopharma Inc., Kanagawa, Japan.

Kotaro Shirakawa (K)

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Akifumi Takaori-Kondo (A)

Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Kosuke Yusa (K)

Stem Cell Genetics, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Japan.

Tadashi Asakura (T)

Radioisotope Research Facilities, Jikei University School of Medicine, Tokyo, Japan.

Hideaki Kakeya (H)

Department of System Chemotherapy and Molecular Sciences, Division of Medicinal Frontier Sciences, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan. Electronic address: scseigyo-hisyo@pharm.kyoto-u.ac.jp.

Masashi Kanai (M)

Department of Therapeutic Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan. Electronic address: kanai@kuhp.kyoto-u.ac.jp.

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Classifications MeSH