Feb 7, 2008

2-Methoxyestradiol reverses doxorubicin resistance in human breast tumor xenograft

Cancer Chemotherapy and Pharmacology
Samar S AzabAshraf B Abdel-Naim

Abstract

2-Methoxyestradiol (2ME), an endogenous estradiol metabolite, was developed as a novel agent based on its antitumor activity and lack of toxicity. This study was designed to investigate the modulatory effect of 2ME on the antitumor effect of doxorubicin (Dox) in resistant breast tumor xenograft. Resistant MCF-7/Dox cells were implanted subcutaneously in nude mice Treatment with Dox 5 mg/kg, 2ME 30 mg/kg and their combination continued twice a week for 2 weeks. Following 28 days from starting the treatment with Dox alone, the change in tumor volume from first day of treatment was 455.6 +/- 16.2%. Combined Dox and 2ME treatment significantly reduced tumor volume to 20.8 +/- 43%. Also, combined therapy resulted in enhanced tumor apoptotic and reduced proliferative activities relative to Dox alone. The apoptotic indices were 0.13 +/- 0.03 and 0.75 +/- 0.06 in Dox alone and Dox + 2ME groups, respectively. For Dox alone group, expression of the proliferative markers PCNA and Ki67 were 0.78 +/- 0.06 and 0.63 +/- 0.18, respectively. They were significantly reduced to 0.28 +/- 0.1 and 0.12 +/- 0.1 for their corresponding combined Dox and 2ME group. Interaction analysis clearly indicated that 2ME synergies antitumor, apoptotic and anti-p...Continue Reading

Mentioned in this Paper

Doxorubicin
Biological Markers
Study
Xenograft Model Antitumor Assays
Antibiotic Resistance, Neoplasm
Apoptosis, Intrinsic Pathway
Mice, Inbred BALB C
Anti-Angiogenesis Effect
Panzem
Estradiol, (16 alpha,17 beta)-Isomer

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