Reversible Effects on Cellular Metabolism and Proliferation by Trisodium Phosphonoformate
Open Access
- 1 November 1978
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 14 (5) , 727-730
- https://doi.org/10.1128/aac.14.5.727
Abstract
The antiviral compound trisodium phosphonoformate (PFA), which inhibits herpesvirus multiplication by 50% at a concentration of 10 μM, did not show any effects on macromolecular synthesis and cell proliferation in HeLa and human lung cells at this concentration. At the high concentration of 2 mM, PFA reduced DNA synthesis to 50% after 1 h of treatment, whereas no effects could be seen on RNA and protein synthesis. Treatment for 24 h with 1 mM PFA inhibited both DNA synthesis and cell proliferation to 50%. The inhibition of DNA synthesis and cell proliferation at 10 mM PFA was rapidly reversed by removing the drug from the cells.This publication has 5 references indexed in Scilit:
- Therapeutic Effect of Trisodium Phosphonoformate on Cutaneous Herpesvirus Infection in Guinea PigsAntimicrobial Agents and Chemotherapy, 1978
- Trisodium Phosphonoformate, a New Antiviral CompoundScience, 1978
- Inhibition of eucaryotic DNA polymerases by phosphonoacetate and phosphonoformateArchives of Biochemistry and Biophysics, 1978
- Inhibition of Herpesvirus Replication and Herpesvirus-Induced Deoxyribonucleic Acid Polymerase by PhosphonoformateAntimicrobial Agents and Chemotherapy, 1978
- Reversible Inhibition of Cellular Metabolism by RibavirinAntimicrobial Agents and Chemotherapy, 1978