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Vol. 299, Issue 2, 426-433, November 2001
College of Pharmacy and James Cancer Hospital and Solove Research
Institute, The Ohio State University, Columbus, Ohio
We recently reported that acidic and basic fibroblast growth factors
(aFGF and bFGF) confer a broad-spectrum chemoresistance in solid
tumors, and that inhibitors of these proteins enhanced the antitumor
activity of several anticancer drugs. The present study
investigated the effect of FGF inhibitors on doxorubicin activity in
human prostate PC3 tumors. In in vitro studies, conditioned medium (CM)
obtained from histocultures of rat MAT-LyLu lung metastases and
different combinations of recombinant FGF induced a 7- to 15-fold
doxorubicin resistance. Suramin had no effect on the doxorubicin activity in the absence of CM or FGF, but reversed the CM- and FGF-induced resistance by
90% at concentrations that had no
cytotoxicity (i.e., 1-17 µM suramin). In the in vivo study,
immunodeficient mice bearing well established, subcutaneous PC3 tumors
(~100 mg in size) were treated intravenously with doxorubicin (5 mg/kg) and suramin (10 mg/kg), administered twice weekly for 3 weeks. The suramin dose, selected to yield plasma concentration of below 50 µM, had neither antitumor activity nor toxicity. Doxorubicin alone
reduced tumor growth rate by ~60%, reduced the density of nonapoptotic tumor cells by ~60%, enhanced the apoptotic cell fraction by 4-fold, and reduced the body weight by ~15%
(p < 0.05 compared with control). Addition of
suramin to doxorubicin therapy did not increase weight loss but
significantly enhanced the antitumor effect, resulting in complete
inhibition of tumor growth, an additional 3-fold reduction in the
density of nonapoptotic tumor cells, and an additional 2-fold
enhancement of the apoptotic tumor cell fraction (p < 0.05 compared with all other groups). These data indicate significant enhancement of the effectiveness of doxorubicin in prostate
tumors by nontoxic and subtherapeutic doses of suramin.
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