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Dietary Influence on Pancreatic Cancer Growth by Catechin and Inositol Hexaphosphate

Authors :
McMillan, Brian
Riggs, Dale R.
Jackson, Barbara J.
Cunningham, Cynthia
McFadden, David W.
Source :
Journal of Surgical Research. Jul2007, Vol. 141 Issue 1, p115-119. 5p.
Publication Year :
2007

Abstract

Introduction: Pancreatic cancer is an extremely virulent form of cancer with few effective treatments. Catechin and inositol hexaphosphate (IP6), two naturally occurring molecules found in green tea and high-fiber foods, respectively, are compounds that have been shown to demonstrate anti-proliferative effects when administered as single therapeutic agents against a number of cancers. We hypothesized that, alone and in combination, IP6 and catechin would be effective against pancreatic cancer. Materials and methods: Pancreatic (PANC-1 and MIAPACA) cancer cell lines were cultured and treated with IP6 (0.8 mm/well), catechin (100uM/well), and the combination of the two. Cell viability was measured by 3-(4,5-dimethylthiazol-2-y1)-2,5-diphenyltetrazolium bromide (MTT) at 24, 48, and 72 h. Vascular endothelial growth factor (VEGF) was measured in the cell supernatants by ELISA. Apoptosis was evaluated by Annexin V-fluorescein isothiocyanate (FITC). Results: The combination of catechin and IP6 significantly inhibited proliferation in the PANC-1 cell line at 24, 48, and 72 h compared to single agents (P < 0.001). Growth of the MIAPACA cell line was inhibited (P < 0.01) by each agent alone, but additive inhibitory effects were not seen. An increase in early apoptosis was attributed to catechin therapy in both cell lines (P < 0.01). The combination of these agents also increased early apoptotic activity when compared to the control (P < 0.001). IP6 reduced VEGF in both cell lines (P < 0.01). In combination, catechin and IP6 amplified VEGF reduction compared to each agent in MIAPACA and control (P < 0.002). Conclusions: These results, combined with the prevalence of these compounds in safe, naturally occurring foods, make catechin and IP6 attractive therapies for treatment, and possibly in preventative trials, of pancreatic cancer. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00224804
Volume :
141
Issue :
1
Database :
Academic Search Index
Journal :
Journal of Surgical Research
Publication Type :
Academic Journal
Accession number :
25407724
Full Text :
https://doi.org/10.1016/j.jss.2007.03.065