Epigallocatechin-3-gallate promotes apoptosis and expression of the caspase 9a splice variant in PC3 prostate cancer cells

  • Authors:
    • Rachel M. Hagen
    • Veronica S. Chedea
    • Christopher P. Mintoff
    • Elizabeth Bowler
    • H. Ruth Morse
    • Michael R. Ladomery
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  • Published online on: April 24, 2013     https://doi.org/10.3892/ijo.2013.1920
  • Pages: 194-200
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Abstract

Growing evidence suggests that the flavonoid epigallocatechin-3-gallate (EGCG), notably abundant in green tea, has health-promoting properties. We examined the effect of EGCG on cell survival and apoptosis in the prostate cancer cell line PC3. Cell survival was reduced and apoptosis increased significantly with a low dose of 1 µM EGCG. The ability of the anticancer drug cisplatin to promote apoptosis was enhanced by EGCG. Furthermore, EGCG, both alone and in combination with cisplatin, promoted the expression of the pro-apoptotic splice isoform of caspase 9.
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July 2013
Volume 43 Issue 1

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
Hagen RM, Chedea VS, Mintoff CP, Bowler E, Morse HR and Ladomery MR: Epigallocatechin-3-gallate promotes apoptosis and expression of the caspase 9a splice variant in PC3 prostate cancer cells. Int J Oncol 43: 194-200, 2013
APA
Hagen, R.M., Chedea, V.S., Mintoff, C.P., Bowler, E., Morse, H.R., & Ladomery, M.R. (2013). Epigallocatechin-3-gallate promotes apoptosis and expression of the caspase 9a splice variant in PC3 prostate cancer cells. International Journal of Oncology, 43, 194-200. https://doi.org/10.3892/ijo.2013.1920
MLA
Hagen, R. M., Chedea, V. S., Mintoff, C. P., Bowler, E., Morse, H. R., Ladomery, M. R."Epigallocatechin-3-gallate promotes apoptosis and expression of the caspase 9a splice variant in PC3 prostate cancer cells". International Journal of Oncology 43.1 (2013): 194-200.
Chicago
Hagen, R. M., Chedea, V. S., Mintoff, C. P., Bowler, E., Morse, H. R., Ladomery, M. R."Epigallocatechin-3-gallate promotes apoptosis and expression of the caspase 9a splice variant in PC3 prostate cancer cells". International Journal of Oncology 43, no. 1 (2013): 194-200. https://doi.org/10.3892/ijo.2013.1920