A Water-Soluble Hydrogen Sulfide Donor Suppresses the Growth of Hepatocellular Carcinoma Via Inhibiting the AKT/GSK-3/-Catenin and TGF-/Smad2/3 Signaling Pathways

Overview

Journal J Oncol

Specialty Oncology

Date 2023 Mar 17

PMID 36925651

Authors

Shao-Feng Duan

Meng-Meng Zhang

Qian Dong

Bo Yang

Wei Liu

Xin Zhang

Hai-Lan Yu

Shi-Hui Zhang

Nazeer Hussain Khan

Dong-Dong Wu

Xiao-Ju Zhang

Juan Cen

Affiliations

Soon will be listed here.

Abstract

Hepatocellular carcinoma (HCC) is a disease with high morbidity, high mortality, and low cure rate. Hyaluronic acid (HA) is widely adopted in tissue engineering and drug delivery. 5-(4-Hydroxyphenyl)-3H-1, 2-dithiol-3-thione (ADT-OH) is one of commonly used HS donors. In our previous study, HA-ADT was designed and synthesized via coupling of HA and ADT-OH. In this study, compared with sodium hydrosulfide (NaHS, a fast HS-releasing donor) and morpholin-4-ium (4-methoxyphenyl)-morpholin-4-ylsulfanylidenesulfido-5-phosphane (GYY4137, a slow HS-releasing donor), HA-ADT showed stronger inhibitory effect on the proliferation, migration, invasion, and cell cycle of human HCC cells. HA-ADT promoted apoptosis by suppressing the expressions of phospho (p)-protein kinase B (PKB/AKT), p-glycogen synthase kinase-3 (GSK-3), p--catenin, and also inhibited autophagy via the downregulation of the protein levels of p-Smad2, p-Smad3, and transforming growth factor- (TGF-) in human HCC cells. Moreover, HA-ADT inhibited HCC xenograft tumor growth more effectively than both NaHS and GYY4137. Therefore, HA-ADT can suppress the growth of HCC cells by blocking the AKT/GSK-3/-catenin and TGF-/Smad2/3 signaling pathways. HA-ADT and its derivatives may be developed as promising antitumor drugs.

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