Τόμος 20 (2006) – Τεύχος 2 – Άρθρο 6 – Επιθεώρηση Κλινικής Φαρμακολογίας και Φαρμακοκινητικής-Διεθνής Έκδοση – Volume 20 (2006) – Issue 2 – Article 6 – Epitheorese Klinikes Farmakologias και Farmakokinetikes-International Edition

Title Cytogenetic efficacy by modified steroidal esters of N-acetyl melphalan
Authors Eleni Dima¹,², Eleftheria Mioglou¹, Zafeiroula Iakovidou¹, Katerina Spyridonidou², Sotiris Nikolaropoulos² and Dionysios Mourelatos¹

1.      Laboratory of Biology and Genetics, Medical School, Aristotle University, 54124 Thessaloniki, Greece

2.      Laboratory of Medicinal Chemistry, Dept. of Pharmacy, University of Patras, Rion-Patras, Greece

Citation Dima, E., Mioglou, E., Iakovidou, Z., Spyridonidou, P., Nikolaropoulos, S. et al: Cytogenetic efficacy by modified steroidal esters of N-acetyl melphalan, Epitheorese Klin. Farmakol. Farmakokinet. 20(2): 85-87 (2006)
Publication Date Accepted for publication: 19-20 May 2006
Full Text Language English
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Keywords Steroidal esters of N-Acetyl melphalan, cytogenetic effects.
Other Terms review article
Summary Melphalan (L-PAM) has been used widely in cancer chemotherapy but in many cases a diversity of toxic side effects have been reported. The chemical linkage with a steroidal moiety has been proven one of the most effective strategies in order to reduce the high toxicity and ameliorate the selectivity of alkylating agents. Six newly synthesized N-Ac-Melphalan esters with modified steroidal skeletons at D and/or B ring have been tested, on a molar basis (0.1 and 0.2 µM) for cytogenetic activity in normal human lymphocyte cultures. SCEs have been used as the most sensitive indicator of DNA damage and/or subsequent repair and PR/ as a very valuable index of cytostatic effects. All derivatives induced a dose dependent significant increase (P<0.001) in SCE frequency and the most effective proved the 7-17-diketo compound. A correlation was observed between the magnitude of SCE response and the PR/ depression (r = -0.55, and P<0.02). Ιt is of interest that N-Ac-Melphalan and Melphalan at 0.1 µM were inactive, while the six steroidal derivatives proved quite effective.
References 1. Van Putten L.M., Lelieveld P.: Factors determining cell killing by chemotherapeutic agents in vivo-II. Melphalan, Chlorambucil and Nitrogen Mustard. Europ. J. Cancer 7: 11-16 (1971)

2. Goldenberg G.J., Lam H.Y., Begleiter A.: (1979) Active carrier-mediated transport of melphalan by two abeling amino acid transport systems in LPC-1 plasmacytoma cells in vitro. J. Biol. Chem. 254: 1057-1064 (1979)

3. Larrivee B., D.A. Averill D.A.: (1999) Melphalan resistance and photoaffinity abeling of

P-glycoprotein in multidrug-resistant Chinese hamster ovary cells: reversal of resistance by cyclosporin A and hyperthermia. Biochem. Pharmacol. 58: 291-302 (1999)

4. Karayianni V., Papageorgiou A., Mioglou E., et. al.: 7-Keto hybrid steroidal esters of nitrogen mustard: cytogenetic and antineoplastic effects. Anti-Cancer Drugs: 637-643 (2002)

5. Fousteris M.A., Koutsourea A.I., Arsenou E.S., et. al.: Antileucemic and cytogenetic effects of modified and non-modified esteric steroidal derivatives of 4-methyl-3-bis(2-chloro-ethyl)amino benzoic acid. (4-Me-CABA). Anticancer Res, 22, 2293-2300 (2002)

6. Mourelatos D.: Chromosomes study as pre or of chemoresponse of tumors. Cancer J. 9: 136-141 (1996)

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