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PURPOSE: Because effective drug delivery is often limited by inadequate vasculature within the tumor, the ability to modulate the tumor microenvironment is one strategy that may achieve better drug distribution. We have previously shown that treatment of mice bearing tumors with phosphoinositide-3 kinase (PI3K) inhibitors alters vascular structure in a manner analogous to vascular normalization and results in increased perfusion of the tumor. On the basis of that result, we asked whether inhibition of PI3K would improve chemotherapy delivery. EXPERIMENTAL DESIGN: Mice with xenografts using the cell line SQ20B bearing a hypoxia marker or MMTV-neu transgenic mice with spontaneous breast tumors were treated with the class I PI3K inhibitor GDC-0941. The tumor vasculature was evaluated by Doppler ultrasound, and histology. The delivery of doxorubicin was assessed using whole animal fluorescence, distribution on histologic sections, high-performance liquid chromatography on tumor lysates, and tumor growth delay. RESULTS: Treatment with GDC-0941 led to approximately three-fold increases in perfusion, substantially reduced hypoxia and vascular normalization by histology. Significantly increased amounts of doxorubicin were delivered to the tumors correlating with synergistic tumor growth delay. The GDC-0941 itself had no effect on tumor growth. CONCLUSION: Inhibition of PI3K led to vascular normalization and improved delivery of a chemotherapeutic agent. This study highlights the importance of the microvascular effects of some novel oncogenic signaling inhibitors and the need to take those changes into account in the design of clinical trials many of which use combinations of chemotherapeutic agents.

Original publication

DOI

10.1158/1078-0432.CCR-11-1413

Type

Journal article

Journal

Clin Cancer Res

Publication Date

01/01/2012

Volume

18

Pages

161 - 169

Keywords

Animals, Doxorubicin, Drug Delivery Systems, Female, Humans, Hypoxia, Immunoenzyme Techniques, Indazoles, Mammary Neoplasms, Animal, Mice, Mice, Nude, Mice, Transgenic, Microvessels, Neovascularization, Pathologic, Phosphatidylinositol 3-Kinases, Sulfonamides