http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004018186-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1b18f15bd3b53b2bedd230661191441c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-51
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-51
filingDate 2003-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ebb93da3f4f0a141ceeb037256cad15
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ce3116f86bf7c4d1049bac7d7494586
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f668e30c37d7adf335b775d6d5aba51c
publicationDate 2004-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004018186-A1
titleOfInvention Attenuation of tumor growth, metastasis and angiogenesis
abstract A highly purified and specific glycosaminoglycan degrading enzyme, chondroitinase AC, and to a lesser extent, chondroitinase B, can be used in the treatment of metastatic cancers and in other disorders characterized by angiogenesis. The enzymatic removal of chondroitin sulfates A and C, and to a lesser extent, chondroitin sulfate B, from cell surfaces directly decreases the ability of tumor cells to invade blood vessels and thus prevents the formation of metastatic, or secondary tumors; inhibits tumor cell growth; and decreases angiogenesis by inhibiting both endothelial cell proliferation and capillary formation. Decreasing the formation of new blood vessels into the tumor in turn decreases the potential for tumor growth, and further decreases the ability of tumor cells to invade the bloodstream. These effects are opposite to the pro-metastatic effects of tumor-secreted heparanase.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2015274815-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2012237504-A1
priorityDate 1999-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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