Tumors treated with anti-Flk-1 mAb have increased tumor cell apoptosis, reduced tumor cell proliferation, and increased tumor necrosis. s.c. Tumors treated.

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Tumors treated with anti-Flk-1 mAb have increased tumor cell apoptosis, reduced tumor cell proliferation, and increased tumor necrosis. s.c. Tumors treated with anti-Flk-1 mAb have increased tumor cell apoptosis, reduced tumor cell proliferation, and increased tumor necrosis. s.c. A431 tumors after 2 weeks of antibody therapy were resected, fixed, embedded in paraffin or frozen, and sectioned onto glass slides. Shown are representative sections from the DC101 group (A–C) and for the control IgG group (D–F). A and D, H&E staining of paraffin sections showed extensive areas of necrosis and fibrosis in tumors from DC101-treated animals. B and E, sections were immunostained with a mAb to PCNA (brown) and counterstained with eosin Y. The number of mitotic A431 tumor cells was significantly greater in tumors from control mice compared to tumors from DC101-treated animals. C and F, frozen sections of tumor tissue were assayed for apoptosis using a TUNEL kit that labels apoptotic nuclei with a fluorescent marker (green). A markedly higher frequency of apoptotic A431 tumor cells was found in tumors from DC101-treated animals. × 200. Marie Prewett et al. Cancer Res 1999;59:5209-5218 ©1999 by American Association for Cancer Research