Gambogic Acid Inhibits Wnt/β-catenin Signaling and Induces ER Stress-Mediated Apoptosis in Human Cholangiocarcinoma.

Autor:	Suksen K; Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand., Janpipatkul K; Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.; Department of Basic Medical Science, Faculty of Medicine Vajira Hospital, Navamindradhiraj University, Bangkok, Thailand., Reabroi S; Department of Pharmacology, Faculty of Science, Mahidol University, Bangkok, Thailand., Anantachoke N; Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand., Reutrakul V; Department of Chemistry and Center of Excellence for Innovation in Chemistry (PERCH-CIC), Faculty of Science, Mahidol University, Bangkok, Thailand., Chairoungdua A; Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.; Excellent Center for Drug Discovery (ECDD), Mahidol University, Bangkok, Thailand.; Toxicology Graduate Program, Faculty of Science, Mahidol University, Bangkok, Thailand.; Center of Excellence on Environmental Health and Toxicology (EHT), Faculty of Science, Mahidol University, Bangkok, Thailand., Thongon N; Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand., Bhukhai K; Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Jazyk:	angličtina
Zdroj:	Asian Pacific journal of cancer prevention : APJCP [Asian Pac J Cancer Prev] 2021 Jun 01; Vol. 22 (6), pp. 1913-1920. Date of Electronic Publication: 2021 Jun 01.
DOI:	10.31557/APJCP.2021.22.6.1913
Abstrakt:	Objective: Gambogic acid (GA) has been reported to induce apoptosis in cholangiocarcinoma (CCA) cell lines. However, the molecular mechanisms underlying its anti-cancer activity remain poorly understood. This study was aimed to investigate GA's effect on human CCA cell lines, KKU-M213 and HuCCA-1, and its associated mechanisms on Wnt/β-catenin signaling pathway. Methods: Cell viability, apoptosis, and cell cycle analysis were conducted by MTT and flow cytometry. The effect of GA mediated Wnt/β-catenin and ER stress were determined by luciferase-reporter assay, qRT-PCR, and western blot analysis. Results: GA exhibited potent cytotoxicity in CCA cells which was associated with significantly inhibited cell proliferation, promoted G1 arrest, and activated caspase 3 mediated-apoptosis. GA attenuated β-catenin transcriptional levels, decreased β-catenin protein, and suppressed the expression of c-Myc, a downstream target gene of Wnt/β-catenin signaling. GA activated genes involved in ER stress mechanism in KKU-M213 and enhanced CCA's sensitivity to gemcitabine. Conclusion: Our findings reveal that the molecular mechanism underpinning anti-cancer effect of GA is partially mediated through the inhibition of Wnt/β-catenin signaling pathway and induction of ER stress induced-apoptosis. GA may serve as a promising therapeutic modality for amelioration of gemcitabine-induced toxicity in CCA.
Databáze:	MEDLINE
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