Procyanidin B1, a novel and specific inhibitor of Kv10.1 channel, suppresses the evolution of hepatoma.

Abstract

Recently, we and other groups revealed that aberrant expression of Kv10.1 channel, a voltage-gated potassium ion channel, contributes to a variety of tumorigenesis process.Potent and selective inhibitor of Kv10.1 is urgently needed, both as pharmacological tools for studying the physiological functions of this enigmatic channel and as potential leads for development of anti-tumor drugs. In this study, Procyanidin B1, a natural compound extracted from the grape seed, was identified as a potent, specific inhibitor, which can inhibit the Kv10.1 channel in a concentration-dependent manner (IC50 = 10.38 ± 0.87 μM), but has negligible effects on other potassium channels, including Kir2.1, HERG or KCNQ1. It was demonstrated that Procyanidin B1 directly binds to Kv10.1 channel and inhibits its currents, without increasing intracellular Ca2+. Further, three amino acids, I550, T552, and Q557 in the C-linker domain of Kv10.1 were found critical for forming the binding pocket of Procyanidin B1 with Kv10.1 channel.In addition, Procyanidin B1 inhibits migration and proliferation of liver cancer cells (HuH-7 cells, HepG2 cells) through inhibiting Kv10.1, but not in Kv10.1 negatively expressed cell lines. Next, we assayed the tumor suppressing effect of Procyanidin B1 on cell line-derived xenograft mouse model. Our data showed that 15 mg/kg Procyanidin B1 can significantly suppress the growth of the tumor (HepG2) with an inhibition rate of about 60.25%. Compared with cisplatin, Procyanidin B1 has no side effect on the normal metabolismof the mice. The present work indicated that Procyanidin B1 is a proming liver cancer anti-tumor drug, and also confirmed that Kv10.1 can serve as a potential, tumor-specific drug target.

• Authors: Wenjing Na, Biao Ma, Sai Shi, Yafei Chen, Hailin Zhang, Yong Zhan, Hailong An
• Journal: Biochemical pharmacology (Biochem Pharmacol) Vol. 178 Pg. 114089 (08 2020) ISSN: 1873-2968 [Electronic] England
• PMID: 32533968 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2020 Elsevier Inc. All rights reserved.

Chemical References

• Biflavonoids
• Ether-A-Go-Go Potassium Channels
• KCNH1 protein, human
• Proanthocyanidins
• procyanidin B1
• Catechin

Topics

• Animals
• Biflavonoids (pharmacology, therapeutic use)
• Carcinogenesis (drug effects, metabolism)
• Carcinoma, Hepatocellular (drug therapy, metabolism)
• Catechin (pharmacology, therapeutic use)
• Ether-A-Go-Go Potassium Channels (antagonists & inhibitors, chemistry, metabolism)
• HEK293 Cells
• Hep G2 Cells
• Humans
• Liver Neoplasms (diet therapy, metabolism)
• Male
• Mice
• Mice, Inbred BALB C
• Proanthocyanidins (pharmacology, therapeutic use)
• Protein Structure, Secondary
• Protein Structure, Tertiary
• Tumor Burden (drug effects, physiology)
• Xenograft Model Antitumor Assays (methods)