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[Cancer Research 43, 5151-5155, November 1, 1983]
© 1983 American Association for Cancer Research

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In Vivo Antitumor Activity of the Bitter Melon (Momordica charantia)1

Catherine Jilka, Beth Strifler, G. William Fortner, Esther F. Hays and Dolores J. Takemoto2

Department of Biochemistry [C. J., B. S., D. J. T.] and Division of Biology [G. W. F.], Kansas State University, Manhattan, Kansas 66506, and Laboratory of Biomolecular and Environmental Sciences, University of California, Los Angeles, California 90024 [E. F. H.]

The in vivo antitumor activity of a crude extract from the bitter melon (Momordica charantia) was determined. The extract inhibited tumor formation in CBA/H mice which had been given i.p. injections of 1.0 x 105 CBA/DI tumor cells (77% of the untreated mice with tumors versus 33% of the treated mice with tumors after 6 weeks). The extract also inhibited tumor formation in DBA/2 mice which had been given i.p. injections of either 1 x 105 P388 tumor cells (0% of untreated mice survived after 30 days versus 40% survival of the treated mice) or 1 x 105 L1210 tumor cells (0% survival of untreated mice versus 100% of treated mice after 30 days). The in vivo antitumor effect required both the prior exposure of tumor cells to the extract (2 hr) in vitro and i.p., biweekly injections of the extract into the mice. The optimum dose for tumor inhibition (8 µg protein, biweekly, i.p.) was not toxic to mice for at least 45 days of treatment. This same treatment caused a marked enhancement of C3H mouse thymic cell response to concanavalin A in vitro. When compared to the untreated control mice, the bitter melon-injected animals exhibited a 4-fold-higher incorporation of tritiated thymidine into trichloroacetic acid-precipitable material after 48 hr of exposure to 50 µg of concanavalin A. Nylon wool-purified spleen cells from these same bitter melon-treated mice exhibited an enhanced mixed lymphocyte reaction when exposed to irradiated P388 stimulator cells (186% of the untreated control mice). These data indicate that in vivo enhancement of immune functions may contribute to the antitumor effects of the bitter melon extract.

1 This research was supported by NIH Grants CA 27500 and CA 24196 and by a special fellowship from the Leukemia Society of America. This is Publication 83-156-j from the Kansas Agricultural Experiment Station.

2 To whom requests for reprints should be addressed.

Received 4/25/83. Accepted 7/29/83.







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
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1983 by the American Association for Cancer Research.