Garlic compound, diallyl disulfide induces cell cycle arrest in prostate cancer cell line PC-3

被引:49
作者
Arunkumar, Arumugam [1 ]
Vijayababu, Marati Radhakrishnan [1 ]
Srinivasan, Narasimman [1 ]
Aruldhas, Maria Michael [1 ]
Arunakaran, Jagadeesan [1 ]
机构
[1] Univ Madras, Post Grad Inst Basic Med Sci, Dept Endocrinol, Madras 600113, Tamil Nadu, India
关键词
cell cycle arrest; cyclins; cyclin dependent kinase; diallyl disulfide; prostate cancer;
D O I
10.1007/s11010-006-9126-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prostate cancer is the most predominant cancer in men and related death rate increases every year. Till date, there is no effective therapy for androgen independent prostate cancer. Previous studies reported that aged garlic extract suppresses cancer growth. In the present study, diallyl disulfide [DADS], oil soluble organosulfur compound of garlic, was studied for its antiproliferative and induction of cell cycle arrest on prostate cancer cells in vitro. The suppression of cell growth was assessed by MTT assay. Induction of cell cycle arrest was assessed and confirmed by propidium iodide staining in flowcytometric analysis and western blotting analysis of major cell cycle regulator proteins. The results showed that DADS inhibited the growth of prostate cancer cells in a dose dependent manner, compared to the control. At 25 mu M and 40 mu M concentrations, DADS induced cell cycle arrest at G2/M transition in PC-3 cells. Western blotting analysis of cyclin A, B-1 and cyclin dependent kinase 1 [CDK1] revealed that DADS inhibited the cell cycle by downregulating CDK1 expression. It is concluded that DADS, inhibits proliferation of prostate cancer cells through cell cycle arrest. Dose dependent effect of DADS on PC-3 cell line was observed in the present study.
引用
收藏
页码:107 / 113
页数:7
相关论文
共 42 条
[2]   Growth suppressing effect of garlic compound diallyl disulfide on prostate cancer cell line (PC-3) in vitro [J].
Arunkumar, A ;
Vijayababu, MR ;
Kanagaraj, P ;
Balasubramanian, K ;
Aruldhas, MM ;
Arunakaran, J .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2005, 28 (04) :740-743
[3]   The future of prostate cancer prevention [J].
Brawley, OW ;
Barnes, S ;
Parnes, H .
CANCER PREVENTION: MOLECULAR MECHANISMS TO CLINICAL APPLICATIONS, 2001, 952 :145-152
[4]   LATENT CARCINOMA OF PROSTATE AT AUTOPSY IN 7 AREAS - COLLABORATIVE STUDY ORGANIZED BY INTERNATIONAL-AGENCY-FOR-RESEARCH-ON-CANCER, LYONS, FRANCE [J].
BRESLOW, N ;
CHAN, CW ;
DHOM, G ;
DRURY, RAB ;
FRANKS, LM ;
GELLEI, B ;
LEE, YS ;
LUNDBERG, S ;
SPARKE, B ;
STERNBY, NH ;
TULINIUS, H .
INTERNATIONAL JOURNAL OF CANCER, 1977, 20 (05) :680-688
[5]   Initiation of a G2/M checkpoint after ultraviolet radiation requires p38 kinase [J].
Bulavin, DV ;
Higashimoto, Y ;
Popoff, IJ ;
Gaarde, WA ;
Basrur, V ;
Potapova, O ;
Appella, E ;
Fornace, AJ .
NATURE, 2001, 411 (6833) :102-107
[6]   CDC2 REGULATORY FACTORS [J].
COLEMAN, TR ;
DUNPHY, WG .
CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (06) :877-882
[7]   GARLIC - A REVIEW OF ITS RELATIONSHIP TO MALIGNANT DISEASE [J].
DAUSCH, JG ;
NIXON, DW .
PREVENTIVE MEDICINE, 1990, 19 (03) :346-361
[8]   Diallyl disulfide (DADS) increases histone acetylation and p21waf1/cip1 expression in human colon tumor cell lines [J].
Druesne, N ;
Pagniez, A ;
Mayeur, C ;
Thomas, M ;
Cherbuy, C ;
Duée, PH ;
Martel, P ;
Chaumontet, C .
CARCINOGENESIS, 2004, 25 (07) :1227-1236
[9]   REVIEW - PROSTATE-CANCER EPIDEMIOLOGY [J].
FLANDERS, WD .
PROSTATE, 1984, 5 (06) :621-629
[10]  
GUNADHARINI DN, 2005, CELL BIOCH FUNC, V23, P1