http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2011045291-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_82787c2fee17b0b0eb295d5af7d2325f
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7088
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-113
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2009-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efbaf38eefcc4aa8a9f1fc165ecaafff
publicationDate 2011-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2011045291-A
titleOfInvention Dexamethasone-induced protein gene region, anticancer drug resistance discrimination kit, anticancer drug sensitivity recovery method, anticancer drug composition, siRNA, apoptosis recovery composition
abstract A gene region of a marker for determining resistance to an anticancer drug is provided. [Solution] An anticancer drug resistance determination method is provided. A novel function of the dexamethasone-induced protein gene was identified. In this dexamethasone-induced protein gene, the promoter region is methylated. When the expression of dexamethasone-induced protein decreases due to this methylation, apoptosis due to a caspase cascade is suppressed. For this reason, the present invention is characterized by detecting methylation of the dexamethasone-induced protein gene region of cancer cells and determining that it is resistant to an anticancer drug when the methylation is performed. [Selection] Figure 1
priorityDate 2009-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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