Carcinogenesis Advance Access originally published online on March 19, 2004
Carcinogenesis 2004 25(8):1409-1415; doi:10.1093/carcin/bgh149
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Carcinogenesis vol.25 no.8 © Oxford University Press 2004; all rights reserved.
ARTICLE |
Allyl-isothiocyanate causes mitotic block, loss of cell adhesion and disrupted cytoskeletal structure in HT29 cells
Institute of Food Research, Norwich Research Park, Colney, Norwich NR4 7UA, UK
1 To whom correspondence should be addressed Email: liz.lund{at}bbsrc.ac
Epidemiological evidence indicates that Brassica vegetables protect against colorectal cancer. Brassicas contain glucosinolates, the breakdown products of which exert antiproliferative effects against cancer cells. We have examined the effects of allyl-isothiocyanate (AITC), a major breakdown product of the glucosinolate sinigrin, on proliferation and death of colorectal cancer cells. HT-29 colorectal cells were exposed to AITC for 24 h and the number of adherent and detached cells determined. Both populations were analysed for cell-cycle characteristics and examined by light and electron microscopy for features of apoptosis and mitosis. Evidence of apoptosis was also determined by flow cytometric analysis of Annexin V staining in the detached population of cells. AITC-treated cells were also stained for
-tubulin. Treatment caused cells to round up after 7 h of exposure and subsequently detach. At 24 h these cells were blocked in mitosis. Detached AITC-treated cells showed no signs of apoptosis as assessed by morphological features or by Annexin V staining but they did show evidence of disrupted tubulin. AITC inhibits proliferation of cancer cells by causing mitotic block associated with disruption of
-tubulin in a manner analogous to a number of chemotherapeutic agents.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
B. B. Aggarwal, M. E. Van Kuiken, L. H. Iyer, K. B. Harikumar, and B. Sung Molecular Targets of Nutraceuticals Derived from Dietary Spices: Potential Role in Suppression of Inflammation and Tumorigenesis Experimental Biology and Medicine, August 1, 2009; 234(8): 825 - 849. [Abstract] [Full Text] [PDF] |
||||
![]() |
U. Telang, D. A. Brazeau, and M. E. Morris Comparison of the Effects of Phenethyl Isothiocyanate and Sulforaphane on Gene Expression in Breast Cancer and Normal Mammary Epithelial Cells Experimental Biology and Medicine, March 1, 2009; 234(3): 287 - 295. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Ragasa, E. Nakamura, L. Marrone, S. Yanaka, S. Hayashi, K. Takeuchi, and S. J. Hagen Isothiocyanate Inhibits Restitution and Wound Repair after Injury in the Stomach: Ex Vivo and in Vitro Studies J. Pharmacol. Exp. Ther., October 1, 2007; 323(1): 1 - 9. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Zhang, S. Loganathan, I. Humphreys, and S. K. Srivastava Benzyl Isothiocyanate-Induced DNA Damage Causes G2/M Cell Cycle Arrest and Apoptosis in Human Pancreatic Cancer Cells J. Nutr., November 1, 2006; 136(11): 2728 - 2734. [Abstract] [Full Text] [PDF] |
||||


