PT  - JOURNAL ARTICLE
AU  - LI LI
AU  - NILS-ERIK HELDIN
AU  - JAN GRAWÉ
AU  - ULF ULMSTEN
AU  - XIN FU
TI  - Induction of Apoptosis or Necrosis in Human Endometrial Carcinoma Cells by 2-Methoxyestradiol
DP  - 2004 Nov 01
TA  - Anticancer Research
PG  - 3983--3990
VI  - 24
IP  - 6
4099  - http://ar.iiarjournals.org/content/24/6/3983.short
4100  - http://ar.iiarjournals.org/content/24/6/3983.full
SO  - Anticancer Res2004 Nov 01; 24
AB  - Background: We investigated the effects of 2-methoxyestradiol (2-ME), an endogenous estrogenic metabolite, on human endometrial cancer HEC-1-A and RL-95-2 cell lines. Materials and Methods: After exposure of HEC-1-A and RL-95-2 cells to 2-ME, the morphological changes were evaluated by acridine orange staining and transmission electron microscopy. Cell cycle progress, apoptosis and necrosis were assessed by flow cytometry, DNA fragmentation and Western blot. Results: 2-ME inhibited cell growth by blocking the S- and G2/M-phase in both cell lines, by inducing apoptosis in HEC-1-A cells and by causing necrosis in RL-95-2 cells. Apoptosis, on HEC-1-A cells, was accompanied by an increased expression of iNOS and STAT1. This apoptotic effect was prevented by the iNOS inhibitor 1400W and eliminated by the caspase inhibitor Z-VAD-FMK. Necrosis, on RL-95-2 cells, was due to a severe disruption of the mitochondrial membrane potential. 2-ME had no significant effect on normal human endometrial cells. Conclusion: The data suggest that 2-ME has an antitumor effect on human endometrial carcinoma cells (HEC-1-A and RL-95-2) and may contribute as a new therapeutic agent for endometrial cancer patients. Copyright© 2004 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved