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Research Paper

Antitumor Effects of a Natural Anthracycline Analog (Aloin) Involve Altered Activity of Antioxidant Enzymes in HeLaS3 Cells

Ana Niciforovic, Miroslav Adzic, Snezana D. Spasic and Marija B. Radojcic

volume 6 | issue 8

August 2007
Pages: 1200 - 1205

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The antiproliferative and cytotoxic potential of the natural anthracycline aloin from Aloe vera was tested on human uterine carcinoma HeLaS3 cells. Aloin showed a pronounced antiproliferative effect at physiological concentration (IC50=97μM), caused cell cycle arrest in the S phase, and markedly increased HeLaS3 cell apoptosis (to 24%). In the concentration range of 20-100 μM, its action was accompanied by remarkable changes in the activity of almost all antioxidant enzymes: MnSOD activity was increased many fold, while CuZnSOD and iNOS activities were inhibited. Moreover, inhibition of CuZnSOD was shown to occur by direct aloin interaction with the enzyme. As catalase activity was not changed, it is suggested that such conditions were responsible for antiproliferative and cytotoxic effects owing to accumulation of H2O2. Aloin alone was a more potent proapoptotic agent than a 2 Gy fractional dose of ionizing radiation or a combination of the two. Compared to other currently used therapeutics, aloin, due to its less undesirable side effects and antimetastatic potential, may prove to be the agent of choice on which clinical protocols for the treatment of human cervical carcinoma should rely in future.

Authors

Ana Niciforovic

Department of Molecular Biology and Endocrinology, VINCA Institute of Nuclear Sciences, Belgrade, Serbia

Miroslav Adzic

Department of Molecular Biology and Endocrinology, VINCA Institute of Nuclear Sciences, Belgrade, Serbia

Snezana D. Spasic

Centre of Chemistry, ICHTM, Belgrade, Serbia

Marija B. Radojcic

Department of Molecular Biology and Endocrinology, VINCA Institute of Nuclear Sciences, Belgrade, Serbia




We now provide open access to journal articles published online for one year or more. This article may be downloaded at the following link:

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