| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Division of Biophysics, Sloan-Kettering Institute for Cancer Research, New York, New York 10021
Exposure of HeLa S-3 cells to 10-3 M hydroxyurea for a period of 16 hr produced a loss of cell viability accompanied by an inhibition of DNA synthesis. Continued synthesis of RNA and protein suggests an unbalanced growth similar to that previously observed with 5-fluorodeoxyuridine, excess thymidine, and 1-ß-D-arabinofuranosylcytosine. A threefold increase in thymidine kinase activity was observed as a result of unbalanced growth following the exposure of cells to hydroxyurea. When cells were exposed to 10-2 M hydroxyurea for short exposure times, however, appreciable loss of cell viability occurred only for those cells in the DNA synthetic phase.
1 This work was aided by grants from the National Cancer Institute (CA 08748) and the Atomic Energy Commission (AT (30-1)-910).
Received 12/29/66. Accepted 3/27/67.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Cancer Research | Clinical Cancer Research |
| Cancer Epidemiology Biomarkers & Prevention | Molecular Cancer Therapeutics |
| Molecular Cancer Research | Cancer Prevention Research |
| Cancer Prevention Journals Portal | Cancer Reviews Online |
| Annual Meeting Education Book | Meeting Abstracts Online |