Combined effects on tumor growth and metastasis by anti-estrogenic and antiangiogenic therapies in MMTV-neu mice
Breast tumor growth and metastasization are both hormone-sensitive and angiogenesis-dependent. Recent work carried out in our laboratory on a transgenic model of breast cancer displaying many similarities to its human counterpart, has shown that liposome-mediated angiostatin cDNA delivery partially...
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description | Breast tumor growth and metastasization are both hormone-sensitive and angiogenesis-dependent. Recent work carried out in our laboratory on a transgenic model of breast cancer displaying many similarities to its human counterpart, has shown that liposome-mediated angiostatin cDNA delivery partially inhibits both local and metastatic growth. However, it is now recognized that anti-angiogenesis strategy alone cannot completely arrest tumor growth and spread, and this led to the suggestion that approaches based on different molecular mechanisms could usefully be combined. In the present work, we investigated whether tamoxifen, a classical antiestrogen agent widely used in human therapy, could improve the results obtained with angiostatin alone. Further reduction of local growth was achieved with the combined regimen with respect to angiostatin or tamoxifen alone, while, as expected, no metastatic growth was detected in either group. We therefore conclude that a combination of angiogenesis inhibitors with antiestrogen drugs might be useful in humans and that other associations between conventional and gene transfer-mediated therapy are worth investigating and will soon become important components of anticancer therapy. |
doi_str_mv | 10.1038/sj.gt.3301817 |
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G ; SOLDATI, S ; MIRA CATO, E ; CATTANEO, L ; PRATESI, G ; SCANZIANI, E ; VEZZONI, P</creator><creatorcontrib>SACCO, M. G ; SOLDATI, S ; MIRA CATO, E ; CATTANEO, L ; PRATESI, G ; SCANZIANI, E ; VEZZONI, P</creatorcontrib><description>Breast tumor growth and metastasization are both hormone-sensitive and angiogenesis-dependent. Recent work carried out in our laboratory on a transgenic model of breast cancer displaying many similarities to its human counterpart, has shown that liposome-mediated angiostatin cDNA delivery partially inhibits both local and metastatic growth. However, it is now recognized that anti-angiogenesis strategy alone cannot completely arrest tumor growth and spread, and this led to the suggestion that approaches based on different molecular mechanisms could usefully be combined. In the present work, we investigated whether tamoxifen, a classical antiestrogen agent widely used in human therapy, could improve the results obtained with angiostatin alone. Further reduction of local growth was achieved with the combined regimen with respect to angiostatin or tamoxifen alone, while, as expected, no metastatic growth was detected in either group. We therefore conclude that a combination of angiogenesis inhibitors with antiestrogen drugs might be useful in humans and that other associations between conventional and gene transfer-mediated therapy are worth investigating and will soon become important components of anticancer therapy.</description><identifier>ISSN: 0969-7128</identifier><identifier>EISSN: 1476-5462</identifier><identifier>DOI: 10.1038/sj.gt.3301817</identifier><identifier>PMID: 12224018</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Angiogenesis ; Angiogenesis inhibitors ; Angiogenesis Inhibitors - genetics ; Angiogenesis Inhibitors - metabolism ; Angiostatin ; Angiostatins ; Animals ; Antiestrogens ; Antineoplastic Agents, Hormonal - therapeutic use ; Applied cell therapy and gene therapy ; Biological and medical sciences ; Biotechnology ; Breast cancer ; Combined Modality Therapy ; DNA, Complementary - genetics ; Female ; Fundamental and applied biological sciences. Psychology ; Gene therapy ; Gene transfer ; Genetic Therapy - methods ; Gynecology. Andrology. Obstetrics ; Health. Pharmaceutical industry ; Industrial applications and implications. Economical aspects ; Lung Neoplasms - prevention & control ; Lung Neoplasms - secondary ; Mammary gland diseases ; Mammary Neoplasms, Experimental - blood supply ; Mammary Neoplasms, Experimental - drug therapy ; Mammary Neoplasms, Experimental - therapy ; Medical sciences ; Metastases ; Metastasis ; Mice ; Mice, Transgenic ; Molecular modelling ; Neovascularization, Pathologic - prevention & control ; Peptide Fragments - genetics ; Peptide Fragments - metabolism ; Plasminogen - genetics ; Plasminogen - metabolism ; Tamoxifen ; Tamoxifen - therapeutic use ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy ; Tumors ; Xenoestrogens</subject><ispartof>Gene therapy, 2002-10, Vol.9 (19), p.1338-1341</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Oct 2002</rights><rights>Macmillan Publishers Limited 2002.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-96fa9537193cd72a4b5be2a1ba8f46ce01562b6ce54a381fa96fa2f2e5e0f9dc3</citedby><cites>FETCH-LOGICAL-c444t-96fa9537193cd72a4b5be2a1ba8f46ce01562b6ce54a381fa96fa2f2e5e0f9dc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13946976$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12224018$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SACCO, M. G</creatorcontrib><creatorcontrib>SOLDATI, S</creatorcontrib><creatorcontrib>MIRA CATO, E</creatorcontrib><creatorcontrib>CATTANEO, L</creatorcontrib><creatorcontrib>PRATESI, G</creatorcontrib><creatorcontrib>SCANZIANI, E</creatorcontrib><creatorcontrib>VEZZONI, P</creatorcontrib><title>Combined effects on tumor growth and metastasis by anti-estrogenic and antiangiogenic therapies in MMTV-neu mice</title><title>Gene therapy</title><addtitle>Gene Ther</addtitle><description>Breast tumor growth and metastasization are both hormone-sensitive and angiogenesis-dependent. Recent work carried out in our laboratory on a transgenic model of breast cancer displaying many similarities to its human counterpart, has shown that liposome-mediated angiostatin cDNA delivery partially inhibits both local and metastatic growth. However, it is now recognized that anti-angiogenesis strategy alone cannot completely arrest tumor growth and spread, and this led to the suggestion that approaches based on different molecular mechanisms could usefully be combined. In the present work, we investigated whether tamoxifen, a classical antiestrogen agent widely used in human therapy, could improve the results obtained with angiostatin alone. Further reduction of local growth was achieved with the combined regimen with respect to angiostatin or tamoxifen alone, while, as expected, no metastatic growth was detected in either group. We therefore conclude that a combination of angiogenesis inhibitors with antiestrogen drugs might be useful in humans and that other associations between conventional and gene transfer-mediated therapy are worth investigating and will soon become important components of anticancer therapy.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Angiogenesis</subject><subject>Angiogenesis inhibitors</subject><subject>Angiogenesis Inhibitors - genetics</subject><subject>Angiogenesis Inhibitors - metabolism</subject><subject>Angiostatin</subject><subject>Angiostatins</subject><subject>Animals</subject><subject>Antiestrogens</subject><subject>Antineoplastic Agents, Hormonal - therapeutic use</subject><subject>Applied cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Breast cancer</subject><subject>Combined Modality Therapy</subject><subject>DNA, Complementary - genetics</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene therapy</subject><subject>Gene transfer</subject><subject>Genetic Therapy - methods</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Health. Pharmaceutical industry</subject><subject>Industrial applications and implications. Economical aspects</subject><subject>Lung Neoplasms - prevention & control</subject><subject>Lung Neoplasms - secondary</subject><subject>Mammary gland diseases</subject><subject>Mammary Neoplasms, Experimental - blood supply</subject><subject>Mammary Neoplasms, Experimental - drug therapy</subject><subject>Mammary Neoplasms, Experimental - therapy</subject><subject>Medical sciences</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Molecular modelling</subject><subject>Neovascularization, Pathologic - prevention & control</subject><subject>Peptide Fragments - genetics</subject><subject>Peptide Fragments - metabolism</subject><subject>Plasminogen - genetics</subject><subject>Plasminogen - metabolism</subject><subject>Tamoxifen</subject><subject>Tamoxifen - therapeutic use</subject><subject>Transfusions. Complications. 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Cell therapy and gene therapy</topic><topic>Angiogenesis</topic><topic>Angiogenesis inhibitors</topic><topic>Angiogenesis Inhibitors - genetics</topic><topic>Angiogenesis Inhibitors - metabolism</topic><topic>Angiostatin</topic><topic>Angiostatins</topic><topic>Animals</topic><topic>Antiestrogens</topic><topic>Antineoplastic Agents, Hormonal - therapeutic use</topic><topic>Applied cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Breast cancer</topic><topic>Combined Modality Therapy</topic><topic>DNA, Complementary - genetics</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene therapy</topic><topic>Gene transfer</topic><topic>Genetic Therapy - methods</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Health. Pharmaceutical industry</topic><topic>Industrial applications and implications. Economical aspects</topic><topic>Lung Neoplasms - prevention & control</topic><topic>Lung Neoplasms - secondary</topic><topic>Mammary gland diseases</topic><topic>Mammary Neoplasms, Experimental - blood supply</topic><topic>Mammary Neoplasms, Experimental - drug therapy</topic><topic>Mammary Neoplasms, Experimental - therapy</topic><topic>Medical sciences</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Molecular modelling</topic><topic>Neovascularization, Pathologic - prevention & control</topic><topic>Peptide Fragments - genetics</topic><topic>Peptide Fragments - metabolism</topic><topic>Plasminogen - genetics</topic><topic>Plasminogen - metabolism</topic><topic>Tamoxifen</topic><topic>Tamoxifen - therapeutic use</topic><topic>Transfusions. Complications. Transfusion reactions. 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G</au><au>SOLDATI, S</au><au>MIRA CATO, E</au><au>CATTANEO, L</au><au>PRATESI, G</au><au>SCANZIANI, E</au><au>VEZZONI, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined effects on tumor growth and metastasis by anti-estrogenic and antiangiogenic therapies in MMTV-neu mice</atitle><jtitle>Gene therapy</jtitle><addtitle>Gene Ther</addtitle><date>2002-10-01</date><risdate>2002</risdate><volume>9</volume><issue>19</issue><spage>1338</spage><epage>1341</epage><pages>1338-1341</pages><issn>0969-7128</issn><eissn>1476-5462</eissn><abstract>Breast tumor growth and metastasization are both hormone-sensitive and angiogenesis-dependent. Recent work carried out in our laboratory on a transgenic model of breast cancer displaying many similarities to its human counterpart, has shown that liposome-mediated angiostatin cDNA delivery partially inhibits both local and metastatic growth. However, it is now recognized that anti-angiogenesis strategy alone cannot completely arrest tumor growth and spread, and this led to the suggestion that approaches based on different molecular mechanisms could usefully be combined. In the present work, we investigated whether tamoxifen, a classical antiestrogen agent widely used in human therapy, could improve the results obtained with angiostatin alone. Further reduction of local growth was achieved with the combined regimen with respect to angiostatin or tamoxifen alone, while, as expected, no metastatic growth was detected in either group. We therefore conclude that a combination of angiogenesis inhibitors with antiestrogen drugs might be useful in humans and that other associations between conventional and gene transfer-mediated therapy are worth investigating and will soon become important components of anticancer therapy.</abstract><cop>Basingstoke</cop><pub>Nature Publishing Group</pub><pmid>12224018</pmid><doi>10.1038/sj.gt.3301817</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Angiogenesis Angiogenesis inhibitors Angiogenesis Inhibitors - genetics Angiogenesis Inhibitors - metabolism Angiostatin Angiostatins Animals Antiestrogens Antineoplastic Agents, Hormonal - therapeutic use Applied cell therapy and gene therapy Biological and medical sciences Biotechnology Breast cancer Combined Modality Therapy DNA, Complementary - genetics Female Fundamental and applied biological sciences. Psychology Gene therapy Gene transfer Genetic Therapy - methods Gynecology. Andrology. Obstetrics Health. Pharmaceutical industry Industrial applications and implications. Economical aspects Lung Neoplasms - prevention & control Lung Neoplasms - secondary Mammary gland diseases Mammary Neoplasms, Experimental - blood supply Mammary Neoplasms, Experimental - drug therapy Mammary Neoplasms, Experimental - therapy Medical sciences Metastases Metastasis Mice Mice, Transgenic Molecular modelling Neovascularization, Pathologic - prevention & control Peptide Fragments - genetics Peptide Fragments - metabolism Plasminogen - genetics Plasminogen - metabolism Tamoxifen Tamoxifen - therapeutic use Transfusions. Complications. Transfusion reactions. Cell and gene therapy Tumors Xenoestrogens |
title | Combined effects on tumor growth and metastasis by anti-estrogenic and antiangiogenic therapies in MMTV-neu mice |
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