Anti-cancer effects of the aqueous extract of Orostachys japonica A. Berger on 5-fluorouracil-resistant colorectal cancer via MAPK signalling pathways in vitro and in vivo

被引:6
|
作者
Kim, Jung Woo [1 ]
Kim, Sang Hee [2 ]
Mariappan, Ramesh [3 ]
Moon, Daeun [4 ]
Kim, Jinu [4 ,5 ]
Yoon, Sang-Pil [5 ]
机构
[1] KIM JUNG WOO R&D Lab, Namwon 55790, Jeollabuk Do, South Korea
[2] Korea Food Res Inst, Div Creat Food Sci Hlth, Jeollabuk Do 55365, South Korea
[3] Chosun Univ, Coll Med, Dept Cellular & Mol Med, Gwangju 61452, South Korea
[4] Jeju Natl Univ, Interdisciplinary Grad Program Adv Convergence Te, Jeju 63243, South Korea
[5] Jeju Natl Univ, Coll Med, Dept Anat, Jeju 63243, South Korea
关键词
Colorectal cancer; Orostachys japonica; MAPK; Xenograft; Gallic acid; CELL-CYCLE ARREST; APOPTOSIS; INDUCTION; FRACTION; INHIBITION; FLAVONOIDS; RESISTANT; AKT; ERK;
D O I
10.1016/j.jep.2021.114412
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Orostachys japonica A. Berger, also known as Wa-song in Korea, has traditionally been used as a folk medicine, but the potential anti-cancer effects of aqueous extract of Orostachys japonica (OJe) have not yet been thoroughly investigated. Aim of the study: To evaluate the anti-cancer effects of OJe, its possible mechanisms of action were investigated in 5-fluorouracil (5-FU) resistant SNU-C5/5-FUR colorectal cancer cells. Materials and methods: The functional compounds of OJe were identified with high performance liquid chromatography. The anti-cancer effects of OJe in SNU-C5/5-FUR cells were investigated by a cell viability assays, flow cytometry analysis, and a subcutaneous xenograft model employing BALB/c-nude mice. Possible signalling pathways were assayed with Western blotting. Results: OJe (250 mu g/ml) showed anti-cancer effects in SNU-C5/5-FUR cells, that were mediated via apoptosis as well as cell cycle arrest at the G0/G1 phase. Gallic acid and (-)-epicatechin, the major functional components of OJe, induced cell cycle arrest. OJe treatment (250 mg/kg, p.o.) produced a significant anti-proliferative effect in the xenograft model via decreased 8-catenin/GSK38 and increased p27 expression. OJe treatment significantly activated ERK and p38 both in vitro and in vivo. Conclusions: These results suggest that OJe has anti-proliferative effects on 5-FU-resistant colorectal cancer cells via regulation of MAPK signalling pathways.
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页数:11
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