Use of interferon and medroxyprogesterone acetate for the treatment of endometrial cancer

  • Authors:
    • R Angioli
    • B Sevin
    • M Untch
    • O Kochli
    • R Estape
    • H Averette
  • View Affiliations

  • Published online on: March 1, 1996     https://doi.org/10.3892/or.3.2.351
  • Pages: 351-354
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Abstract

Endometrial cancer is a hormone sensitive tumor. Response rate to progestational therapy is related to steroid receptor expression of the tumor. Interferons have been shown to enhance hormonal receptors. In this study the effect of four different interferons and medroxyprogesterone acetate (MPA), on three human endometrial cancer cell lines (AE-7, HEC-1A and HEC-1B), was studied. The ATP cell viability assay was used to measure the antiproliferative activity of the agents used. Synergistic effect was noted only when interferons and MPA were used in combination for the treatment of AE-7, which is the only cell line with a high baseline level of progesterone receptors. These observations indicate that the use of interferons and MPA may have a role for the treatment of endometrial cancer patients with progesterone receptor positive cells.

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March 1996
Volume 3 Issue 2

Print ISSN: 1021-335X
Online ISSN:1791-2431

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Spandidos Publications style
Angioli R, Sevin B, Untch M, Kochli O, Estape R and Averette H: Use of interferon and medroxyprogesterone acetate for the treatment of endometrial cancer. Oncol Rep 3: 351-354, 1996
APA
Angioli, R., Sevin, B., Untch, M., Kochli, O., Estape, R., & Averette, H. (1996). Use of interferon and medroxyprogesterone acetate for the treatment of endometrial cancer. Oncology Reports, 3, 351-354. https://doi.org/10.3892/or.3.2.351
MLA
Angioli, R., Sevin, B., Untch, M., Kochli, O., Estape, R., Averette, H."Use of interferon and medroxyprogesterone acetate for the treatment of endometrial cancer". Oncology Reports 3.2 (1996): 351-354.
Chicago
Angioli, R., Sevin, B., Untch, M., Kochli, O., Estape, R., Averette, H."Use of interferon and medroxyprogesterone acetate for the treatment of endometrial cancer". Oncology Reports 3, no. 2 (1996): 351-354. https://doi.org/10.3892/or.3.2.351