Establishment of high-throughput drug screening cell models based on JAK-STAT signal pathway / 药学学报
Yao Xue Xue Bao
; (12): 164-167, 2004.
Article
de Zh
| WPRIM
| ID: wpr-301123
Bibliothèque responsable:
WPRO
ABSTRACT
<p><b>AIM</b>To discover new drugs which may be applied to diseases of the immune system, hemogenesis system diseases and tumors, several high-throughput drug screening cell models based on JAK-STAT signal pathway have been established.</p><p><b>METHODS</b>Four repeats of STAT DNA binding conserved sequences were synthesized, subcloned into pGL-Luc reporter vector and stably transfected into cell lines in vitro. Cell clones with high copy numbers of STAT binding sites and reporter genes were chosen as high-throughput drug screening cell models. The cell models were tested with known anti-allergic drugs and anti-tumor drugs by determining luciferase activity. The reaction was performed in 96 well micro-plates with a final volume of 50 microL.</p><p><b>RESULTS</b>The cell models by performing rapid fluorescence assay were shown to be highly sensitive and stable after testing with cytokine and drugs. The modification of the expression plasmid simplified this method and made it more practical. It also provided good linear correlation, wide range of assay, highly sensitive and good reproducibility.</p><p><b>CONCLUSION</b>The method can be performed by high-throughput drug screening for effective extraction of Chinese traditional herbs.</p>
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Anatomopathologie
/
Pharmacologie
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Protein-tyrosine kinases
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Médicaments issus de plantes chinoises
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Cellules cancéreuses en culture
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Transduction du signal
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Transactivateurs
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Protéines proto-oncogènes
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Carcinome hépatocellulaire
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Antiallergiques
Type d'étude:
Diagnostic_studies
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Prognostic_studies
/
Screening_studies
Limites du sujet:
Humans
langue:
Zh
Texte intégral:
Yao Xue Xue Bao
Année:
2004
Type:
Article