Cleistanthin B causes G1 arrest and induces apoptosis in mammalian cells

被引:0
作者
Kumar, CPP
Pande, G
Shanmugam, G [1 ]
机构
[1] Madurai Kamaraj Univ, Sch Biol Sci, Div Canc Biol, Madurai 625021, Tamil Nadu, India
[2] Ctr Cellular & Mol Biol, Hyderabad 500007, Andhra Pradesh, India
关键词
apoptosis; cell cycle; cleistanthin B; etoposide;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cleistanthin B is a potential anticancer agent isolated from the tropical plant Cleistanthus collinus. We have previously shown that cleistanthin B is clastogenic and induces micronuclei formation and chromosomal aberrations. We now show that this compound inhibits DNA synthesis in Chinese hamster ovary (CHO) cells and induces apoptosis in cervical carcinoma (SiHa) cells. Flow cytometric analysis of cleistanthin treated CHO cells revealed that they were blocked in G1. Cervical carcinoma (SiHa) cells exposed to cleistanthin B shrank, rounded up and had condensed chromatin and fragmented nuclei. DNA isolated from cleistanthin treated cells exhibited the characteristic apoptotic ladder when electrophoresed in agarose gels. These results were confirmed by flow cytometry. Etoposide, a structurally similar compound also induced apoptosis in these cells although with a difference. Etoposide induced apoptosis after permitting cells to enter into S phase, while cleistanthin B stopped entry of cells into S phase and subsequently drove them to apoptosis.
引用
收藏
页码:413 / 419
页数:7
相关论文
共 17 条
[1]  
AFANASEV VN, 1986, FEBS LETT, V194, P347
[2]   ACTIVATION OF PROGRAMMED CELL-DEATH (APOPTOSIS) BY CISPLATIN, OTHER ANTICANCER DRUGS, TOXINS AND HYPERTHERMIA [J].
BARRY, MA ;
BEHNKE, CA ;
EASTMAN, A .
BIOCHEMICAL PHARMACOLOGY, 1990, 40 (10) :2353-2362
[3]  
BHAKUNI DS, 1969, INDIAN EXP BIO, V7, P20
[4]   MECHANISMS OF CELL-DEATH [J].
FAWTHROP, DJ ;
BOOBIS, AR ;
DAVIES, DS .
ARCHIVES OF TOXICOLOGY, 1991, 65 (06) :437-444
[5]  
FRANKFURT OS, 1993, ONCOL RES, V5, P37
[6]   A MAMMALIAN-CELL CYCLE CHECKPOINT PATHWAY UTILIZING P53 AND GADD45 IS DEFECTIVE IN ATAXIA-TELANGIECTASIA [J].
KASTAN, MB ;
ZHAN, QM ;
ELDEIRY, WS ;
CARRIER, F ;
JACKS, T ;
WALSH, WV ;
PLUNKETT, BS ;
VOGELSTEIN, B ;
FORNACE, AJ .
CELL, 1992, 71 (04) :587-597
[7]   APOPTOSIS - BASIC BIOLOGICAL PHENOMENON WITH WIDE-RANGING IMPLICATIONS IN TISSUE KINETICS [J].
KERR, JFR ;
WYLLIE, AH ;
CURRIE, AR .
BRITISH JOURNAL OF CANCER, 1972, 26 (04) :239-+
[8]   APOPTOSIS BY ANTITUMOR AGENTS AND OTHER FACTORS IN RELATION TO CELL-CYCLE CHECKPOINTS [J].
KONDO, S .
JOURNAL OF RADIATION RESEARCH, 1995, 36 (01) :56-62
[9]  
KUMAR CPP, 1996, MUTAGENESIS, V11, P543
[10]   ACTIVATION OF CYCLIN A-DEPENDENT PROTEIN-KINASES DURING APOPTOSIS [J].
MEIKRANTZ, W ;
GISSELBRECHT, S ;
TAM, SW ;
SCHLEGEL, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :3754-3758