Mefloquine targets β-catenin pathway and thus can play a role in the treatment of liver cancer. (May 2018)

• Record Type: Journal Article
• Authors: Li, Yu-Hui; Yang, Shu-Li; Zhang, Guo-Feng; Wu, Jia-Cheng; Gong, Lu-Lu; Ming-Zhong, ; Lin, Rui-Xin
• Is Part Of: Microbial pathogenesis. Volume 118(2018)
• Page Start: 357
• Page End: 360
• Publication Date: 2018-05
• Subjects: Self-renewal -- Proliferation -- Surface marker -- Stem cell; Pathogenic microorganisms -- Periodicals; Pathology, Molecular -- Periodicals; Communicable Diseases -- microbiology -- Periodicals; Communicable Diseases -- parasitology -- Periodicals; Micro-organismes pathogènes -- Périodiques; Pathologie moléculaire -- Périodiques; Electronic journals; 616.9041
• DOI: 10.1016/j.micpath.2018.03.042
• Languages: English
• ISSNs: 0882-4010

Abstract

Abstract: The current study was designed and performed to investigate the effect of mefloquine on the proliferation and tumor formation potential of liver cancer stem cells. CD133 + HepG2 cells were identified using MACS and showed markedly higher tumor formation potential compared to the parental cells. The secondary tumors formed by CD133 + cells were markedly large in size and more in number compared to the parental cells. Mefloquine treatment of CD133 + HepG2 cells inhibited the proliferation selectively in concentration based manner. The rate of proliferation was inhibited to 82 and 12% in parental and CD133 + sphere forming cells, respectively on treatment with 10 μM concentration of mefloquine. The number of secondary tumors formed by primary tumors was decreased significantly on treatment with 10 μM mefloquine concentration. Treatment of the liver cancer stem cells with mefloquine markedly decreased the potential to undergo self-renewal at 10 μM concentration after 48 h. The results from western blot analysis showed significantly higher expression of cancer stem cell molecules β -catenin and cyclin D1 in LCSCs. Treatment of the LCSCs with various concentrations of mefloquine reduced the expression levels of β -catenin and cyclin D1. Administration of the CD133 + cell tumor xenografts in the mice led to the formation of large sized tumors in the control group. However, the tumor growth was inhibited significantly in the mice on treatment with 10 mg/kg doses of mefloquine after day 21. The tumor weight was significantly lower in the animals of mefloquine treatment group compared to the control group. Thus, mefloquine treatment inhibits self-renewal and proliferation potential of cells through targeting β -catenin pathway. Highlights: Mefloquine treatment inhibited CD133 + HepG2 cell proliferation. It decreased liver cancer stem cell self-renewal. It reduced the expression of β -catenin and cyclin D1. The tumor growth was inhibited significantly in the mice on treatment with mefloquine. Tumor weight was lower in rats treated with mefloquine.