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[Cancer Research 52, 3306-3309, June 15, 1992]
© 1992 American Association for Cancer Research

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Flavone Acetic Acid Increases the Antitumor Effect of Hyperthermia in Mice

Yoshihisa Sakaguchi, Yoshihiko Maehara, Hideo Baba, Tetsuya Kusumoto, Keizo Sugimachi1 and Robert A. Newman

Cancer Center of Kyushu University Hospital [Y. S., T. K., K. S.], and Department of Surgery II [Y. M., H. B., K. S.], Faculty of Medicine, Kyushu University, Fukuoka, Japan, and Department of Medical Oncology, The University of Texas, M. D. Anderson Cancer Center, Houston, Texas 77030 [R. A. N.]

The combined effects of flavone acetic acid (FAA), a synthetic flavonoid, and hyperthermia on B16 melanoma cells were investigated. In vitro, FAA alone at concentrations below 100 µg/ml was not cytotoxic with a 60-min exposure at 37°C. Hyperthermia at 43°C for 60 min enhanced the cytotoxicity of FAA only at concentrations over 100 µg/ml. Inhibition of the growth of B16 melanoma solid tumor by FAA and/or hyperthermia was examined in vivo. FAA (100–200 mg/kg) inhibited tumor growth in a dose-dependent manner. The combined treatment of FAA (200 mg/kg) and hyperthermia (43°C, 15 min) significantly inhibited tumor growth compared to a treatment of FAA or hyperthermia alone. The maximum antitumor effect of FAA combined with hyperthermia was obtained when FAA was administered 2 or 4 h before heat. The significantly increased cytotoxicity of FAA combined with hyperthermia seems to relate to specific decreases in tumor blood flow, a reduction in tumor pH, and an increased tumor temperature, without altering pH in the normal tissues. This combined treatment of FAA and hyperthermia warrants further study for treating subjects with solid tumors.

1 To whom requests for reprints should be addressed, at Department of Surgery II, Faculty of Medicine, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812, Japan.

Received 12/ 3/91. Accepted 4/ 6/92.




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M. R. Horsman and D. W. Siemann
Pathophysiologic Effects of Vascular-Targeting Agents and the Implications for Combination with Conventional Therapies
Cancer Res., December 15, 2006; 66(24): 11520 - 11539.
[Abstract] [Full Text] [PDF]




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 © 1992 by the American Association for Cancer Research.