http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102517373-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bfb6c8679694f4116a6957f56d5a1a4f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-10
filingDate 2011-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1101a4361d66a7cb67e44f7cfdc9c295
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e90a459e4b1007c07daf79fac9d21814
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d45f634889f4118d09443445406cf690
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5bae00f09f416dd11b56dd7b826f2f85
publicationDate 2014-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102517373-B
titleOfInvention Antineoplastic drug screening cell model utilizing STAT3 as target and creation and application thereof
abstract The invention provides an antineoplastic drug screening cell model utilizing STAT3 as target, belonging to the field of biomedicine. The model is created by a reporting system carrier containing an STAT3 specific binding sequence on the basis of active cells with constitutive STAT3, and the model is used for screening treatment medicine of carcinomatous changes and tumors caused by STAT3 constitutive activation. The active cells with the constitutive STAT3 are utilized, so the reporter gene in the model cell is situated at an overactive state, and no additional stimulant is necessary; besides, the obtained stable cell model can be directly used for screening the compounds, thereby not only greatly reducing the screening cost, but also simplifying the whole screening process from cell cultivation, STAT3 activation, compound feed and detection to cell cultivation, compound feed and detection, shortening the screening period, reducing the operation steps, and improving the stability, efficiency and usability of the system, so that the model is more suitable for high throughput medicine screening.
priorityDate 2011-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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