CONTEXT: Oleanolic acid (OA) belongs to the triterpenoid compound group existing widely in food, medicinal herbs and other plants. Its effects on gastric cancer cells and the mechanisms involved have not been investigated. OBJECTIVE: This study aimed to substantiate whether OA induces apoptosis of gastric cancer cell line (MKN28) and to elucidate the molecular mechanism involved. MATERIALS AND METHODS: Cell viability was assessed by MTT assay within the range of 0-160 μg/mL. The effects of OA (5, 10 and 20 μg/mL) on apoptosis of MKN28 cells were evaluated by flow cytometry, DNA fragmentation and mitochondrial membrane potential assays. Western blot and FQRT-PCR assays were used to investigate the mechanism of cell apoptosis induced by OA (5 and 10 μg/mL). RESULTS: OA evidently inhibited cell viability with IC50 of 44.8 and 15.9 μg/mL at 12 and 24 h, respectively. Furthermore, OA increased JNK phosphorylation, decreased AKT phosphorylation, but did not affect p38 and ERK phosphorylation in MKN28 cells. In contrast, OA also significantly enhanced the mRNA expression levels of caspase 3, caspase 9 and Apaf-1 in MKN28 cells. CONCLUSION: OA induces apoptosis of MKN28 cells via the mitochondrial pathway regulated by AKT and JNK signaling pathways.
CONTEXT: Oleanolic acid (OA) belongs to the triterpenoid compound group existing widely in food, medicinal herbs and other plants. Its effects on gastric cancer cells and the mechanisms involved have not been investigated. OBJECTIVE: This study aimed to substantiate whether OA induces apoptosis of gastric cancer cell line (MKN28) and to elucidate the molecular mechanism involved. MATERIALS AND METHODS: Cell viability was assessed by MTT assay within the range of 0-160 μg/mL. The effects of OA (5, 10 and 20 μg/mL) on apoptosis of MKN28 cells were evaluated by flow cytometry, DNA fragmentation and mitochondrial membrane potential assays. Western blot and FQRT-PCR assays were used to investigate the mechanism of cell apoptosis induced by OA (5 and 10 μg/mL). RESULTS: OA evidently inhibited cell viability with IC50 of 44.8 and 15.9 μg/mL at 12 and 24 h, respectively. Furthermore, OA increased JNK phosphorylation, decreased AKT phosphorylation, but did not affect p38 and ERK phosphorylation in MKN28 cells. In contrast, OA also significantly enhanced the mRNA expression levels of caspase 3, caspase 9 and Apaf-1 in MKN28 cells. CONCLUSION: OA induces apoptosis of MKN28 cells via the mitochondrial pathway regulated by AKT and JNK signaling pathways.
Authors: Li Xiao Rui; Song Yu Shu; Wu Jing Jun; Chen Zi Mo; Sun Zheng Wu; Liu Shu Min; Lin Yuan; Peng Jin Yong; Song Zhi Cheng; Wang Shi Sheng; Tang Ze Yao Journal: Tumour Biol Date: 2015-11-07
Authors: Yun-Young Sunwoo; Jin-Hee Lee; Ho Yong Jung; Yu Jin Jung; Moon-Seo Park; Yong-An Chung; Lee-So Maeng; Young-Min Han; Hak Soo Shin; Jisoo Lee; Sang In Park Journal: Evid Based Complement Alternat Med Date: 2015-03-10 Impact factor: 2.629
Authors: M Twardziok; D Meierhofer; S Börno; B Timmermann; S Jäger; Sengül Boral; A Eggert; C I Delebinski; G Seifert Journal: BMC Complement Altern Med Date: 2017-04-28 Impact factor: 3.659