Sharoni Y, Teuerstein I, Levy J
Biochem Biophys Res Commun. 1986 Jan 29;134(2):876-82. doi: 10.1016/s0006-291x(86)80501-0.
DMBA-induced rat mammary tumors were used to study the possible association of phosphoinositide phosphorylation to tumor growth. These membranous enzymatic activities were measured during various stages of tumor growth induced by pharmacological manipulation of plasma prolactin level. An increase in phosphorylation of both phosphatidyl inositol and phosphatidyl inositol 4-phosphate preceded the growth induced by prolactin concomitantly with an increase in tyrosine phosphorylation. Good correlation (r = 0.87) existed between the tyrosine kinase activity and phosphatidyl inositol kinase activity of 21 individual tumors taken from animals at different stages of hormonal manipulation. Phosphoinositide phosphorylation was inhibited by quercetin and was not affected by cAMP, similar to tyrosine kinase. Phosphorylation of angiotensin II by tyrosine kinase was inhibited by 0.2 mg/ml phosphatidyl inositol 4 phosphate or phosphatidyl inositol 4,5-bisphosphate.
用二甲基苯蒽(DMBA)诱导的大鼠乳腺肿瘤来研究磷酸肌醇磷酸化与肿瘤生长之间可能存在的关联。在通过药物调节血浆催乳素水平诱导肿瘤生长的各个阶段,对这些膜酶活性进行了测定。在催乳素诱导生长之前,磷脂酰肌醇和磷脂酰肌醇4-磷酸的磷酸化增加,同时酪氨酸磷酸化也增加。从处于激素调节不同阶段的动物身上获取的21个个体肿瘤的酪氨酸激酶活性和磷脂酰肌醇激酶活性之间存在良好的相关性(r = 0.87)。与酪氨酸激酶类似,槲皮素可抑制磷酸肌醇磷酸化,而环磷酸腺苷(cAMP)对其无影响。0.2 mg/ml的磷脂酰肌醇4-磷酸或磷脂酰肌醇4,5-二磷酸可抑制酪氨酸激酶对血管紧张素II的磷酸化作用。