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Research: YAMAMOTO and colleagues,
Listed in Issue 49
Abstract
YAMAMOTO and colleagues, Department of Pathology II, Kansai Medical University, Moriguchi, Osaka, Japan studied the effects of eicosapentaenoic acid (EPA) and an angiogenesis inhibitor (TNP-470) upon breast cancer cell growth in 4 human breast cancer cell lines.
Background
Methodology
The human breast cancer cell lines were MDA-MB-231, T-47D, MDF-7, KPL-1 and MKL-F.
Results
EPA and TNP-470 alone both demonstrated tumour growth inhibition in all five cell lines, in a time- and dose-dependent manner. In combination, a synergistic effect was seen at high concentrations. EPA plus TNP-470 treatment provoked apoptosis, which was verified by the appearance of sub G1 populations, DNA fragmentation and cell morphology. In combination, expression of Bax and Bcl-xS, the apoptosis-enhancing proteins, was more up-regulated that of Bcl-2 and Bcl-xL, the apoptosis-suppressing proteins, was more down-regulated compared to the use of EPA orTNP-470 alone, suggesting that their synergistic effect was due to an acceleration of apoptosis.
Conclusion
References
Yamamoto D et al. Synergistic action of apoptosis induced by eicosapentaenoic acid and TNP-470 on human breast cancer cells. Breast Cancer Research and Treatment 55(2): 149-60. May 1999.
Comment
To a molecular biologist (as I am) it is extremely reassuring when researchers discover how nutrients such as EPA actually suppress cancer growth, at the molecular level. This will filter down into patient care, probably within a 5-year period, when it will probably be possible to induce apoptosis and cause the cancer cells to commit suicide.