An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer
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. B...
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Veröffentlicht in: | ACTA HISTOCHEMICA ET CYTOCHEMICA 2007, Vol.40(5), pp.139-142 |
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creator | Fujita, Mariko Yasuda, Masanori Kitatani, Kanae Miyazawa, Masaki Hirabayashi, Kenichi Takekoshi, Susumu Iida, Tetsuji Hirasawa, Takeshi Murakami, Masaru Mikami, Mikio Ishiwata, Isamu Shimizu, Michio Osamura, R. Yoshiyuki |
description | 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. |
doi_str_mv | 10.1267/ahc.07024 |
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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. 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Yoshiyuki</creatorcontrib><title>An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer</title><title>ACTA HISTOCHEMICA ET CYTOCHEMICA</title><addtitle>Acta Histochem. Cytochem.</addtitle><description>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.</description><subject>clear cell adenocarcinoma</subject><subject>GLUT-1</subject><subject>HIF-1α</subject><subject>rapamycin</subject><subject>VEGF</subject><issn>0044-5991</issn><issn>1347-5800</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpVkdtKAzEQhoMoth4ufIO8QGqOe_BCKdVqQRC0vQ7TJNumtNklmxaKT-WL-EyuVgRvZuD_mW_4ZxC6YnTAeJZfw9IMaE65PEJ9JmROVEHpMepTKiVRZcl66KxtV5SyTpenqMcKziWXqo_ehwHPGpJqcg_J4WFInowgGBfxNDpIGxcSfkuxMxd7PK7NtvVhgeuAnyZjwj4_8Nu2aaJrW1-HGzxJLR42zdobSJ2AqzriV1dFMKmOe_yyg-gh4MOGC3RSwbp1l7_9HM3GD9PRE3l-eZyMhs9kxUuaSAE5KywvbF6IvMqkUkyIjPPSSVFxacsqq6jKqYXSFmZuqORc2HxuhVWGUybO0e2B22znG2dNFynCWjfRbyDudQ1e_3eCX-pFvdOcqayjdYC7A2DVJli4v0mIyZu10939taRafZefP_w5ZglRuyC-AEu4glY</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Fujita, Mariko</creator><creator>Yasuda, Masanori</creator><creator>Kitatani, Kanae</creator><creator>Miyazawa, Masaki</creator><creator>Hirabayashi, Kenichi</creator><creator>Takekoshi, Susumu</creator><creator>Iida, Tetsuji</creator><creator>Hirasawa, Takeshi</creator><creator>Murakami, Masaru</creator><creator>Mikami, Mikio</creator><creator>Ishiwata, Isamu</creator><creator>Shimizu, Michio</creator><creator>Osamura, R. 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subjects | clear cell adenocarcinoma GLUT-1 HIF-1α rapamycin VEGF |
title | An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer |
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