Narayanan U, Hilf R
Department of Biochemistry, University of Rochester, School of Medicine and Dentistry, New York 14642.
Cancer Biochem Biophys. 1992 Nov;13(2):93-101.
The effects of diabetes and insulin administration on certain aspects of phosphoinositide metabolism in R3230AC mammary tumors were studied in vivo. Three weeks after diabetes was induced by streptozotocin, [3H]myoinositol incorporation into PI, PIP and PIP2 was increased in R3230AC tumors, whereas the formation of [3H]IP, [3H]IP2 and [3H]IP3 was decreased. Administration of protamine zinc insulin (3IU, twice daily, for 3 days) to diabetic rats decreased [3H]myoinositol incorporation into phosphoinositides and inositol phosphates in these mammary tumors. The R3230AC tumor from insulin-treated diabetic hosts had lower levels of unmetabolized [3H]-myoinositol compared to tumors from diabetic animals. Enzymatically-dissociated tumor cells from insulin-treated animals displayed decreased myoinositol transport in vitro. These findings suggest that the insulin-induced decrease in the turnover of inositol lipids in vivo in R3230AC mammary tumors could have resulted from the decreased level of [3H]myoinositol in these cells.
在体内研究了糖尿病和胰岛素给药对R3230AC乳腺肿瘤中磷酸肌醇代谢某些方面的影响。用链脲佐菌素诱导糖尿病3周后,R3230AC肿瘤中[3H]肌醇掺入PI、PIP和PIP2增加,而[3H]IP、[3H]IP2和[3H]IP3的形成减少。给糖尿病大鼠注射精蛋白锌胰岛素(3IU,每日两次,共3天)可降低这些乳腺肿瘤中[3H]肌醇掺入磷酸肌醇和肌醇磷酸的量。与糖尿病动物的肿瘤相比,胰岛素治疗的糖尿病宿主的R3230AC肿瘤中未代谢的[3H] - 肌醇水平较低。来自胰岛素治疗动物的酶解离肿瘤细胞在体外显示出肌醇转运减少。这些发现表明,胰岛素诱导的R3230AC乳腺肿瘤体内肌醇脂质周转率降低可能是由于这些细胞中[3H]肌醇水平降低所致。