Grifolin, a potential antitumor natural product from the mushroom Albatrellus confluens, inhibits tumor cell growth by inducing apoptosis in vitro

被引:117
作者
Ye, M
Liu, JK [1 ]
Lu, ZX
Zhao, Y
Liu, SF
Li, LL
Tan, M
Weng, XX
Li, W
Cao, Y
机构
[1] Chinese Acad Sci, Kunming Inst Bot, Dept Phytochem, Kunming 650204, Yunnan, Peoples R China
[2] Cent S Univ, Xiangya Sch Med, Inst Canc Res, Changsha 410078, Hunan, Peoples R China
关键词
antitumor; mushroom grifolin; apoptosis;
D O I
10.1016/j.febslet.2005.05.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Grifolin is a natural biologically active substance isolated from the fresh fruiting bodies of the mushroom Albatrellus confluens. Here, for the first time, we describe a novel activity of grifolin, namely its ability to inhibit the growth of tumor cells by the induction of apoptosis. Grifolin strongly inhibited the growth of tumor cell lines: CNE1, HeLa, MCF7, SW480, K562, Raji and B95-8. Analysis of acridine orange (AO)/ethidium bromide (EB) staining and flow cytometry showed that grifolin possessed apoptosis induction activity to CNE1, HeLa, MCF7 and SW480. Furthermore, the cytochrome c release from mitochondria was detected by confocal microscopy in CNEI cells after a 12 h treatment with grifolin. The increase of caspase-8, 9, 3 activities revealed that caspase was a key mediator of the apoptotic pathway induced by grifolin, and the underexpression of Bcl-2 and up-regulation of Bax resulted in the increase of Bax: Bel-2 ratio, suggesting that Bcl-2 family involved in the control of apoptosis. Owing to the combination of the significant antitumor activity by inducing apoptosis and natural abundance of the compound, grifolin holds the promise of being an interesting antitumor agent that deserves further laboratory and in vivo exploration. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3437 / 3443
页数:7
相关论文
共 33 条
[1]
Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[2]
Regulation of apoptosis by Bcl-2 family proteins [J].
Burlacu, A .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2003, 7 (03) :249-257
[3]
Ding ZW, 2001, HELV CHIM ACTA, V84, P259, DOI 10.1002/1522-2675(20010131)84:1&lt
[4]
259::AID-HLCA259&gt
[5]
3.0.CO
[6]
2-O
[7]
New members of the Bcl-2 family and their protein partners [J].
Farrow, SN ;
Brown, R .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (01) :45-49
[8]
Apoptosis-based drug screening and detection of selective toxicity to cancer cells [J].
Frankfurt, OS ;
Krishan, A .
ANTI-CANCER DRUGS, 2003, 14 (07) :555-561
[9]
Constitutive activation of Stat3 signaling abrogates apoptosis in squamous cell carcinogenesis in vivo [J].
Grandis, JR ;
Drenning, SD ;
Zeng, Q ;
Watkins, SC ;
Melhem, MF ;
Endo, S ;
Johnson, DE ;
Huang, L ;
He, YK ;
Kim, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :4227-4232
[10]
The biochemistry of apoptosis [J].
Hengartner, MO .
NATURE, 2000, 407 (6805) :770-776