Abstract
Hypoxia inducible factor-1α (HIF-1α) predominantly determines the transcriptional activity of HIF-1, which induces the certain genetic expressions to participate in the proliferation and progression of the tumor. It is supposed that HIF-1α is also an extremely important factor in cancer treatment. Based on the results of our recent analyses using ovarian tumors, which indicated the close association of HIF-1α expression with the acquisition of malignancy and the characterization of histology, we further investigated the possibility of a new strategy of cancer therapy that targeted HIF-1α inhibition in the ovarian carcinoma. The cell line HUOCA-II, which originates from the refractory ovarian clear cell adenocarcinoma, was treated with rapamycin. The inhibitory effect of HIF-1α was analyzed by immunohistochemistry and western blotting. It was demonstrated that inhibition of HIF-1α and vascular endothelial growth factor (VEGF) expressions would lead to the down-regulation of tumor cell proliferation. Interestingly, there was little or no change in GLUT-1 expression by rapamycin administration. Thus, the inhibition of GLUT-1 may also be a key for the new strategy of cancer therapy as well as HIF-1α and VEGF. © 2007 The Japan Society of Histochemistry and Cytochemistry.
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Fujita, M., Yasuda, M., Kitatani, K., Miyazawa, M., Hirabayashi, K., Takekoshi, S., … Osamura, R. Y. (2007). An up-to-date anti-cancer treatment strategy focusing on HIF-1α suppression: Its application for refractory ovarian cancer. Acta Histochemica et Cytochemica, 40(5), 139–142. https://doi.org/10.1267/ahc.07024
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