Abstract:
Published evidence from the U.S. and Europe supports the effect of the anticancer drug hydroxyurea against HIV-1, and its potential synergistic effect with ddl. Approved as an oral chemotherapeutic agent for leukemia and other cancers, hydroxyurea acts as a radical free quencher, inhibiting the cellular enzyme ribonucleotide reductase as well as cellular DNA synthesis during the S phase of the cell division, and it may be through this mechanism that hydroxyurea inhibits tumor cell growth. French scientists at the Centre Leon Bernard in Lyon tested hydroxyurea and a related compound, D-aspartic acid beta-hydroxamate alone and in combination with AZT, ddl, or ddC. Total suppression of viral production and total production against the toxic effects induced by viral replication were demonstrated using the combination of either of the two hydroxamates and ddl after 14 days. In test tube experiments conducted at the National Cancer Institute, both hydroxyurea and ddl inhibited or delayed HIV replication in a dose-dependent manner; in combination, they blocked HIV replication by more than 99.9 percent.
Keywords: Didanosine/THERAPEUTIC USE Drug Therapy, Combination DNA Replication/*DRUG EFFECTS Human Hydroxyurea/*PHARMACOLOGY/THERAPEUTIC USE HIV/PHYSIOLOGY HIV Infections/*DRUG THERAPY Leukocytes, Mononuclear/DRUG EFFECTS/VIROLOGY Virus Replication/*DRUG EFFECTS Zalcitabine/THERAPEUTIC USE Zidovudine/THERAPEUTIC USE NEWSLETTER ARTICLE REVIEW 950530
M9551023
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