Antitumor effects of guanosine-analog phosphonates identified by molecular modelling.

Abstract

Aiming to address new drug targets, molecular modelling is gaining increasing importance although the prediction capability of the in silico method is still under debate. For an improved treatment of actinic keratosis and squamous cell carcinoma, inhibitors of human DNA polymerase alpha (pol alpha) are developed by docking nucleoside phosphonate diphosphates into the active site of pol alpha. The most promising prodrugs OxBu and OxHex were then prepared by total synthesis and tested in the squamous cancer cell line SCC25. OxBu and OxHex proved cytotoxic and antiproliferative in the nanomolar concentration range and thus exceeded activity of aphidicolin, the relevant model compound, and 5-fluorouracil, the current standard for the therapy of actinic keratosis. Interestingly, the cytotoxicity in normal human keratinocytes with OxHex was clearly less pronounced and even not detectable with OxBu. Moreover, cytotoxicity of OxBu in particular with the colorectal carcinoma cell line HT29 even surmounted cytotoxicity in SCC25, and other tumor cell lines were influenced, too, by both agents. Taken together, OxBu and OxHex may offer a new approach to cancer therapy, given the agents are sufficiently well tolerated in vivo which is to be suspected beside their chemical structure.

• Authors: Anja Schwanke, Caterina Murruzzu, Barbara Zdrazil, Ralf Zuhse, Maja Natek, Monika Höltje, Hans Christian Korting, Hans-Ulrich Reissig, Hans-Dieter Höltje, Monika Schäfer-Korting
• Journal: International journal of pharmaceutics (Int J Pharm) Vol. 397 Issue 1-2 Pg. 9-18 (Sep 15 2010) ISSN: 1873-3476 [Electronic] Netherlands
• PMID: 20600723 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright 2010 Elsevier B.V. All rights reserved.

Chemical References

• Antineoplastic Agents
• Organophosphonates
• Adenine
• Fluorouracil

Topics

• Adenine (analogs & derivatives, chemical synthesis, chemistry, pharmacology, therapeutic use)
• Antineoplastic Agents (chemical synthesis, pharmacology, therapeutic use)
• Carcinoma, Squamous Cell (drug therapy)
• Cell Line, Tumor
• Fluorouracil (therapeutic use)
• HT29 Cells
• Humans
• Keratinocytes (drug effects)
• Keratosis, Actinic (drug therapy)
• Models, Molecular
• Molecular Dynamics Simulation
• Organophosphonates (chemical synthesis, chemistry, pharmacology, therapeutic use)