Sharoni Y, Radian S, Levy J
FEBS Lett. 1985 Sep 9;189(1):133-6. doi: 10.1016/0014-5793(85)80857-7.
DMBA induced rat mammary tumors were used to study the association of tyrosine protein kinase activity with tumor growth. Pharmacological manipulations of blood prolactin level, by perphenazine and bromocriptine, were used to stimulate or arrest tumor growth, respectively. During perphenazine treatment, a 2-3-fold increase in membranal tyrosine protein kinase activity, measured with angiotensin II as substrate, preceded the 3-4-fold increase in tumor area. At the same time the cAMP-dependent protein kinase activity, measured with kemptide as substrate, did not change.
用二甲基苯蒽(DMBA)诱导的大鼠乳腺肿瘤来研究酪氨酸蛋白激酶活性与肿瘤生长之间的关联。分别使用奋乃静和溴隐亭对血液催乳素水平进行药理学调控,以分别刺激或抑制肿瘤生长。在奋乃静治疗期间,以血管紧张素II为底物测得的膜酪氨酸蛋白激酶活性增加了2 - 3倍,这发生在肿瘤面积增加3 - 4倍之前。与此同时,以肯普肽为底物测得的环磷酸腺苷(cAMP)依赖性蛋白激酶活性没有变化。