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[Cancer Research 36, 143-150, January 1, 1976]
© 1976 American Association for Cancer Research

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Effect of Adriamycin on the Cell Cycle Traverse and Kinetics of Cultured Human Lymphoblasts1

Awtar Krishan2 and Emil Frei, III

Laboratory of Cytokinetics, Sidney Farber Cancer Center and Harvard Medical School, Boston, Massachusetts 02115

Exposure of cultured human lymphoblasts to adriamycin (ADM) (0.1 µg/ml for 24 hr or 0.5 µg/ml for 1 hr) leads to an accumulation of cells with the DNA content of late S and G2. Higher concentrations of ADM (0.5 to 10 µg/ml) inhibit cell cycle traverse. Effect of ADM on cell cycle traverse, cell growth, and incorporation of labeled precursors into DNA is dependent on drug concentration and length of exposure to ADM. Synchronized cells in G1 or G2 part of the cell cycle are less sensitive to ADM than cells in S phase. Similarly, plateau-phase cells are less sensitive to ADM than cells from log-phase cultures.

1 Supported by Grant CA-06516 from the National Cancer Institute.

2 The abbreviations used are: ADM, adriamycin; CHO, Chinese hamster ovary; TdR, thymidine; IMPY, 2,3-dihydro-1H-imidazo[1,2-b]pyrazole; Ll, Labeling index expressed as percentage of cells showing incorporation of labeled thymidine.

Received 5/27/75. Accepted 8/20/75.







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
Copyright © 1976 by the American Association for Cancer Research.