A methoxyflavanone derivative from the Asian medicinal herb (Perilla frutescens) induces p53-mediated G2/M cell cycle arrest and apoptosis in A549 human lung adenocarcinoma

被引:9
作者
Abd El-Hafeez, Amer Ali [1 ]
Fujimura, Takashi [1 ]
Kamei, Rikiya [1 ]
Hirakawa, Noriko [2 ]
Baba, Kenji [2 ]
Ono, Kazuhisa [1 ,3 ]
Kawamoto, Seiji [1 ]
机构
[1] Hiroshima Univ, Grad Sch Adv Sci Matter, Dept Mol Biotechnol, Hiroshima Res Ctr Hlth Aging HiHA, 1-3-1 Kagamiyama, Higashihiroshima 7398530, Japan
[2] Mishima Food Co Ltd, Hiroshima, Japan
[3] Hiroshima Inst Technol, Fac Life Sci, Dept Food Sci & Biotechnol, Hiroshima, Japan
关键词
Apoptosis; Flavanone; G2/M cell cycle arrest; Lung cancer; p53; Perilla frutescens; ENDOPLASMIC-RETICULUM STRESS; CANCER-CELLS; LEAF EXTRACT; DNA-DAMAGE; ROSMARINIC ACID; P53; DEATH; PATHWAYS; GROWTH; MICE;
D O I
10.1007/s10616-017-0116-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Perilla frutescens is an Asian dietary herb consumed as an essential seasoning in Japanese cuisine as well as used for a Chinese medicine. Here, we report that a newly found methoxyflavanone derivative from P. frutescens (Perilla-derived methoxyflavanone, PDMF; 8-hydroxy-5,7-dimethoxyflavanone) shows carcinostatic activity on human lung adenocarcinoma, A549. We found that treatment with PDMF significantly inhibited cell proliferation and decreased viability through induction of G(2)/M cell cycle arrest and apoptosis. The PDMF stimulation induces phosphorylation of tumor suppressor p53 on Ser15, and increases its protein amount in conjunction with up-regulation of downstream cyclin-dependent kinase inhibitor p21(Cip1/Waf1) and proapoptotic caspases, caspase-9 and caspase-3. We also found that small interfering RNA knockdown of p53 completely abolished the PDMF-induced G(2)/M cell cycle arrest, and substantially abrogated its proapoptotic potency. These results suggest that PDMF represents a useful tumor-preventive phytochemical that triggers p53-driven G(2)/M cell cycle arrest and apoptosis.
引用
收藏
页码:899 / 912
页数:14
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