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[Cancer Research 51, 2808-2812, June 1, 1991]
© 1991 American Association for Cancer Research

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Antitumor Activity of a Transforming Growth Factor {alpha}-Pseudomonas Exotoxin Fusion Protein (TGF-{alpha}-PE40)

Lee H. Pai, Maria G. Gallo, David J. FitzGerald and Ira Pastan1

Laboratory of Molecular Biology, Division of Cancer Biology, Diagnosis and Centers, National Cancer Institute, NIH, Bethesda, Maryland 20892

TGF-{alpha}-PE40 is a chimeric protein composed of transforming growth factor {alpha} (TGF-{alpha}) linked to a modified Pseudomonas toxin from which the cell recognition domain has been deleted (PE40). TGF-{alpha}-PE40 has been shown to have cytotoxic effects on human cancer cell lines that express the epidermal growth factor (EGF) receptor on their surface, and when given i.p., it prolongs the survival of nude mice bearing i.p. tumors. Because several normal tissues, including liver, express EGF receptors on their surfaces, it has not been clear that this agent can be used systemically to treat EGF receptor-bearing tumors. In this study, we have delivered TGF-{alpha}-PE40 for 7 days by continuous infusion through a miniosmotic pump placed in the peritoneal cavity of nude immunodeficient mice. Two different human cancer cell lines that express EGF receptors on their surface were implanted s.c. One was A431, an epidermoid carcinoma; the other was DU-145, a prostate carcinoma. By using this mode of continuous i.p. delivery, we were able to achieve a constant serum level of TGF-{alpha}-PE40 that was nontoxic to the mice and yet delayed the growth of both tumors implanted s.c. and caused partial regression of one. We conclude that it is possible to deliver TGF-{alpha}-PE40 systemically and achieve a therapeutic serum level in mice without major toxicity. Although side effects may be expected, this study establishes that there is a therapeutic window for this agent in the therapy of cancers with high numbers of EGF receptors.

1 To whom requests for reprints should be addressed, at National Cancer Institute, NIH, 9000 Rockville Pike, Bldg. 37, Rm. 4E16, Bethesda, MD 20892.

Received 11/14/90. Accepted 3/21/91.




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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 © 1991 by the American Association for Cancer Research.