The angiogenic asset of soft tissue sarcomas: a new tool to discover new therapeutic targets
STS (soft tissue sarcomas) are rare malignant tumours deriving from cells of mesenchymal origin and represent only 1% of all malignant neoplasms. It has been extensively demonstrated that angiogenesis has an important role in cancer malignancy. Particularly, a lot of studies demonstrate the importan...
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description | STS (soft tissue sarcomas) are rare malignant tumours deriving from cells of mesenchymal origin and represent only 1% of all malignant neoplasms. It has been extensively demonstrated that angiogenesis has an important role in cancer malignancy. Particularly, a lot of studies demonstrate the importance of angiogenesis in the development of carcinomas, whereas little is known about the role of angiogenesis in sarcomas and especially in STS. This review aims at summarizing the new discoveries about the nature and the importance of angiogenesis in STS and the new possible therapeutic strategies involved. Only a few studies concerning STS focus on tumour neovascularization and proangiogenic factors and look for a correlation with the patients prognosis/survival. These studies demonstrate that intratumoural MVD (microvessels density) may not accurately represent the angiogenic capacity of STS. Nevertheless, this does not exclude the possibility that angiogenesis could be important in STS. The importance of neoangiogenesis in soft tissue tumours is confirmed by the arising number of publications comparing angiogenesis mediators with clinical features of patients with STS. The efficacy of anti-angiogenic therapies in other types of cancer is well documented. The understanding of the involvement of the angiogenic process in STS, together with the necessity to improve the therapy for this often mortal condition, prompted the exploration of anti-tumour compounds targeting this pathway. In conclusion, this review emphasizes the importance to better understand the mechanisms of angiogenesis in STS in order to subsequently design-specific target therapies for this group of poorly responding tumours. |
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It has been extensively demonstrated that angiogenesis has an important role in cancer malignancy. Particularly, a lot of studies demonstrate the importance of angiogenesis in the development of carcinomas, whereas little is known about the role of angiogenesis in sarcomas and especially in STS. This review aims at summarizing the new discoveries about the nature and the importance of angiogenesis in STS and the new possible therapeutic strategies involved. Only a few studies concerning STS focus on tumour neovascularization and proangiogenic factors and look for a correlation with the patients prognosis/survival. These studies demonstrate that intratumoural MVD (microvessels density) may not accurately represent the angiogenic capacity of STS. Nevertheless, this does not exclude the possibility that angiogenesis could be important in STS. The importance of neoangiogenesis in soft tissue tumours is confirmed by the arising number of publications comparing angiogenesis mediators with clinical features of patients with STS. The efficacy of anti-angiogenic therapies in other types of cancer is well documented. The understanding of the involvement of the angiogenic process in STS, together with the necessity to improve the therapy for this often mortal condition, prompted the exploration of anti-tumour compounds targeting this pathway. In conclusion, this review emphasizes the importance to better understand the mechanisms of angiogenesis in STS in order to subsequently design-specific target therapies for this group of poorly responding tumours.</description><identifier>ISSN: 0144-8463</identifier><identifier>EISSN: 1573-4935</identifier><identifier>DOI: 10.1042/BSR20140075</identifier><identifier>PMID: 25236925</identifier><language>eng</language><publisher>England: Portland Press Ltd The Biochemical Society</publisher><subject>Angiogenesis ; Angiogenesis Inhibitors - therapeutic use ; Antiangiogenics ; Antigens ; Antineoplastic Agents - therapeutic use ; Blood platelets ; Blood vessels ; Cancer ; Epidermal growth factor ; Fibroblast Growth Factor 2 - antagonists & inhibitors ; Fibroblast Growth Factor 2 - metabolism ; Fibroblasts ; Fibrosarcoma ; Humans ; Insulin-like growth factors ; Malignancy ; Matrix Metalloproteinases - metabolism ; Medical prognosis ; Metastasis ; Models, Biological ; Neoplasms ; Neovascularization, Pathologic - metabolism ; Neovascularization, Pathologic - prevention & control ; Permeability ; Placenta Growth Factor ; Pregnancy Proteins - antagonists & inhibitors ; Pregnancy Proteins - metabolism ; Review ; Sarcoma ; Sarcoma - blood supply ; Sarcoma - drug therapy ; Sarcoma - metabolism ; Soft tissues ; Therapeutic targets ; Tumor necrosis factor-TNF ; Tumors ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - antagonists & inhibitors ; Vascular Endothelial Growth Factor A - metabolism ; Vascularization</subject><ispartof>Bioscience reports, 2014-11, Vol.34 (6), p.e00147-e00147</ispartof><rights>2014. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-c5f161b65c583bd204eb596c09472af78ce34aade472293a0ad2f5e5af43bc933</citedby><cites>FETCH-LOGICAL-c521t-c5f161b65c583bd204eb596c09472af78ce34aade472293a0ad2f5e5af43bc933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219423/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219423/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25236925$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rocchi, Laura</creatorcontrib><creatorcontrib>Caraffi, Stefano</creatorcontrib><creatorcontrib>Perris, Roberto</creatorcontrib><creatorcontrib>Mangieri, Domenica</creatorcontrib><title>The angiogenic asset of soft tissue sarcomas: a new tool to discover new therapeutic targets</title><title>Bioscience reports</title><addtitle>Biosci Rep</addtitle><description>STS (soft tissue sarcomas) are rare malignant tumours deriving from cells of mesenchymal origin and represent only 1% of all malignant neoplasms. It has been extensively demonstrated that angiogenesis has an important role in cancer malignancy. Particularly, a lot of studies demonstrate the importance of angiogenesis in the development of carcinomas, whereas little is known about the role of angiogenesis in sarcomas and especially in STS. This review aims at summarizing the new discoveries about the nature and the importance of angiogenesis in STS and the new possible therapeutic strategies involved. Only a few studies concerning STS focus on tumour neovascularization and proangiogenic factors and look for a correlation with the patients prognosis/survival. These studies demonstrate that intratumoural MVD (microvessels density) may not accurately represent the angiogenic capacity of STS. Nevertheless, this does not exclude the possibility that angiogenesis could be important in STS. The importance of neoangiogenesis in soft tissue tumours is confirmed by the arising number of publications comparing angiogenesis mediators with clinical features of patients with STS. The efficacy of anti-angiogenic therapies in other types of cancer is well documented. The understanding of the involvement of the angiogenic process in STS, together with the necessity to improve the therapy for this often mortal condition, prompted the exploration of anti-tumour compounds targeting this pathway. In conclusion, this review emphasizes the importance to better understand the mechanisms of angiogenesis in STS in order to subsequently design-specific target therapies for this group of poorly responding tumours.</description><subject>Angiogenesis</subject><subject>Angiogenesis Inhibitors - therapeutic use</subject><subject>Antiangiogenics</subject><subject>Antigens</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Blood platelets</subject><subject>Blood vessels</subject><subject>Cancer</subject><subject>Epidermal growth factor</subject><subject>Fibroblast Growth Factor 2 - antagonists & inhibitors</subject><subject>Fibroblast Growth Factor 2 - metabolism</subject><subject>Fibroblasts</subject><subject>Fibrosarcoma</subject><subject>Humans</subject><subject>Insulin-like growth factors</subject><subject>Malignancy</subject><subject>Matrix Metalloproteinases - metabolism</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Models, Biological</subject><subject>Neoplasms</subject><subject>Neovascularization, Pathologic - metabolism</subject><subject>Neovascularization, Pathologic - prevention & control</subject><subject>Permeability</subject><subject>Placenta Growth Factor</subject><subject>Pregnancy Proteins - antagonists & inhibitors</subject><subject>Pregnancy Proteins - metabolism</subject><subject>Review</subject><subject>Sarcoma</subject><subject>Sarcoma - blood supply</subject><subject>Sarcoma - drug therapy</subject><subject>Sarcoma - metabolism</subject><subject>Soft tissues</subject><subject>Therapeutic targets</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumors</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - antagonists & inhibitors</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><subject>Vascularization</subject><issn>0144-8463</issn><issn>1573-4935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkc1LHEEQxZugxM0mp9ylIRdBVvt7tj0EoiRREISot0BT01OzOzI7vXb3KP739rJGjJcqqurH4xWPkK-cHXGmxPHp9R_BuGKs0h_IhOtKzpSVeodMylbN5srIPfIppTvGWDmoj2RPaCGNFXpC_t4skcKw6MICh85TSAkzDS1Noc00dymNSBNEH1aQTijQAR9pDqEvhTZd8uEB43a5xAhrHHNRyRAXmNNnsttCn_DLS5-S218_b87OZ5dXvy_OflzOvBY8l9pyw2ujvZ7LuhFMYa2t8cyqSkBbzT1KBdBgGYWVwKARrUYNrZK1t1JOyfet7nqsV9h4HHKE3q1jt4L45AJ07v_L0C3dIjw4JbhVYiNw8CIQw_2IKbtVeQ37HgYMY3LcyEqbiltT0G_v0LswxqG854QVkjPBDCvU4ZbyMaQUsX01w5nbpObepFbo_bf-X9l_MclnYT6TFw</recordid><startdate>20141104</startdate><enddate>20141104</enddate><creator>Rocchi, Laura</creator><creator>Caraffi, Stefano</creator><creator>Perris, Roberto</creator><creator>Mangieri, Domenica</creator><general>Portland Press Ltd The Biochemical Society</general><general>Portland Press Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20141104</creationdate><title>The angiogenic asset of soft tissue sarcomas: a new tool to discover new therapeutic targets</title><author>Rocchi, Laura ; Caraffi, Stefano ; Perris, Roberto ; Mangieri, Domenica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-c5f161b65c583bd204eb596c09472af78ce34aade472293a0ad2f5e5af43bc933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Angiogenesis</topic><topic>Angiogenesis Inhibitors - therapeutic use</topic><topic>Antiangiogenics</topic><topic>Antigens</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Blood platelets</topic><topic>Blood vessels</topic><topic>Cancer</topic><topic>Epidermal growth factor</topic><topic>Fibroblast Growth Factor 2 - antagonists & inhibitors</topic><topic>Fibroblast Growth Factor 2 - metabolism</topic><topic>Fibroblasts</topic><topic>Fibrosarcoma</topic><topic>Humans</topic><topic>Insulin-like growth factors</topic><topic>Malignancy</topic><topic>Matrix Metalloproteinases - metabolism</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Models, Biological</topic><topic>Neoplasms</topic><topic>Neovascularization, Pathologic - metabolism</topic><topic>Neovascularization, Pathologic - prevention & control</topic><topic>Permeability</topic><topic>Placenta Growth Factor</topic><topic>Pregnancy Proteins - antagonists & inhibitors</topic><topic>Pregnancy Proteins - metabolism</topic><topic>Review</topic><topic>Sarcoma</topic><topic>Sarcoma - blood supply</topic><topic>Sarcoma - drug therapy</topic><topic>Sarcoma - metabolism</topic><topic>Soft tissues</topic><topic>Therapeutic targets</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumors</topic><topic>Vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor A - antagonists & inhibitors</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><topic>Vascularization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rocchi, Laura</creatorcontrib><creatorcontrib>Caraffi, Stefano</creatorcontrib><creatorcontrib>Perris, Roberto</creatorcontrib><creatorcontrib>Mangieri, Domenica</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Bioscience reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rocchi, Laura</au><au>Caraffi, Stefano</au><au>Perris, Roberto</au><au>Mangieri, Domenica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The angiogenic asset of soft tissue sarcomas: a new tool to discover new therapeutic targets</atitle><jtitle>Bioscience reports</jtitle><addtitle>Biosci Rep</addtitle><date>2014-11-04</date><risdate>2014</risdate><volume>34</volume><issue>6</issue><spage>e00147</spage><epage>e00147</epage><pages>e00147-e00147</pages><issn>0144-8463</issn><eissn>1573-4935</eissn><abstract>STS (soft tissue sarcomas) are rare malignant tumours deriving from cells of mesenchymal origin and represent only 1% of all malignant neoplasms. It has been extensively demonstrated that angiogenesis has an important role in cancer malignancy. Particularly, a lot of studies demonstrate the importance of angiogenesis in the development of carcinomas, whereas little is known about the role of angiogenesis in sarcomas and especially in STS. This review aims at summarizing the new discoveries about the nature and the importance of angiogenesis in STS and the new possible therapeutic strategies involved. Only a few studies concerning STS focus on tumour neovascularization and proangiogenic factors and look for a correlation with the patients prognosis/survival. These studies demonstrate that intratumoural MVD (microvessels density) may not accurately represent the angiogenic capacity of STS. Nevertheless, this does not exclude the possibility that angiogenesis could be important in STS. The importance of neoangiogenesis in soft tissue tumours is confirmed by the arising number of publications comparing angiogenesis mediators with clinical features of patients with STS. The efficacy of anti-angiogenic therapies in other types of cancer is well documented. The understanding of the involvement of the angiogenic process in STS, together with the necessity to improve the therapy for this often mortal condition, prompted the exploration of anti-tumour compounds targeting this pathway. In conclusion, this review emphasizes the importance to better understand the mechanisms of angiogenesis in STS in order to subsequently design-specific target therapies for this group of poorly responding tumours.</abstract><cop>England</cop><pub>Portland Press Ltd The Biochemical Society</pub><pmid>25236925</pmid><doi>10.1042/BSR20140075</doi><oa>free_for_read</oa></addata></record> |
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subjects | Angiogenesis Angiogenesis Inhibitors - therapeutic use Antiangiogenics Antigens Antineoplastic Agents - therapeutic use Blood platelets Blood vessels Cancer Epidermal growth factor Fibroblast Growth Factor 2 - antagonists & inhibitors Fibroblast Growth Factor 2 - metabolism Fibroblasts Fibrosarcoma Humans Insulin-like growth factors Malignancy Matrix Metalloproteinases - metabolism Medical prognosis Metastasis Models, Biological Neoplasms Neovascularization, Pathologic - metabolism Neovascularization, Pathologic - prevention & control Permeability Placenta Growth Factor Pregnancy Proteins - antagonists & inhibitors Pregnancy Proteins - metabolism Review Sarcoma Sarcoma - blood supply Sarcoma - drug therapy Sarcoma - metabolism Soft tissues Therapeutic targets Tumor necrosis factor-TNF Tumors Vascular endothelial growth factor Vascular Endothelial Growth Factor A - antagonists & inhibitors Vascular Endothelial Growth Factor A - metabolism Vascularization |
title | The angiogenic asset of soft tissue sarcomas: a new tool to discover new therapeutic targets |
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