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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Japan Society of Histochemistry and Cytochemistry
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2156042/ https://www.ncbi.nlm.nih.gov/pubmed/18224245 http://dx.doi.org/10.1267/ahc.07024 |
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author | 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 |
author_facet | 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 |
author_sort | Fujita, Mariko |
collection | PubMed |
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. |
format | Text |
id | pubmed-2156042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Japan Society of Histochemistry and Cytochemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-21560422008-01-25 An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer 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 Acta Histochem Cytochem Note 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. Japan Society of Histochemistry and Cytochemistry 2007-12-18 2007-12-15 /pmc/articles/PMC2156042/ /pubmed/18224245 http://dx.doi.org/10.1267/ahc.07024 Text en Copyright © 2007 AHC This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Note 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 An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer |
title | An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer |
title_full | An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer |
title_fullStr | An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer |
title_full_unstemmed | An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer |
title_short | An Up-to-Date Anti-Cancer Treatment Strategy Focusing on HIF-1α Suppression: Its Application for Refractory Ovarian Cancer |
title_sort | up-to-date anti-cancer treatment strategy focusing on hif-1α suppression: its application for refractory ovarian cancer |
topic | Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2156042/ https://www.ncbi.nlm.nih.gov/pubmed/18224245 http://dx.doi.org/10.1267/ahc.07024 |
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