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Sorafenib,a small-molecule drug for renal cell carcinoma (RCC),targets multiple kinases including inhibiting the serine-threoninekinases Raf-1,B-Raf and the receptor tyrosine kinase activity.The off-target of multiple target drugs may increase the therapeuticpotential of a drug,but they may also cause toxic side-effects.In order to globally elucidate drug mechanism of sorafenib,apharmaceutical proteomic analysis of OS-RC-2 cells under sorafenib treatment was investigated by a SILAC quantitative proteomicmethod.