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视黄酸对神经母细胞瘤中p21ras及其活性调节因子的影响。

Effect of retinoic acid on p21ras and regulators of its activity in neuroblastoma.

作者信息

Burchill S A, Berry P A, Lewis I J

机构信息

Candlelighter's Children's Research Laboratory Imperial Cancer Research Fund, St James' University Hospital, Leeds, U.K.

出版信息

Eur J Cancer. 1995;31A(4):476-81. doi: 10.1016/0959-8049(95)00054-m.

Abstract

p21ras is a membrane-associated guanine nucleotide-binding protein with intrinsic GTPase activity. This protein is important in the regulation of cell growth and differentiation in a number of different cell types. Therefore, the aim of the present study was to examine the role of p21ras and regulators of its activity in the differentiation of neuroblastoma cells induced by retinoic acid (RA). Phosphorylation of p21ras is regulated by the GTPase activity of type I GAP120 and neurofibromin. RA-induced differentiation of the two neuroblastoma cell lines SK-N-SH and IMR-32 was closely related to growth inhibition. Differentiation induced by RA resulted in an increase in both type I GAP120 and neurofibromin mRNAs. This increase was accompanied by a decrease in the activation of p21ras. These results suggest that, in neuroblastoma, activation of p21ras is not associated with RA-induced differentiation. However, the GTPase activating proteins type I GAP120 and neurofibromin may have effector functions in RA-induced differentiation of neuroblastoma.

摘要

p21ras是一种与膜相关的鸟嘌呤核苷酸结合蛋白,具有内在的GTP酶活性。该蛋白在多种不同细胞类型的细胞生长和分化调节中起重要作用。因此,本研究的目的是探讨p21ras及其活性调节剂在视黄酸(RA)诱导的神经母细胞瘤细胞分化中的作用。p21ras的磷酸化受I型GAP120和神经纤维瘤蛋白的GTP酶活性调节。RA诱导的两种神经母细胞瘤细胞系SK-N-SH和IMR-32的分化与生长抑制密切相关。RA诱导的分化导致I型GAP120和神经纤维瘤蛋白mRNA均增加。这种增加伴随着p21ras激活的减少。这些结果表明,在神经母细胞瘤中,p21ras的激活与RA诱导的分化无关。然而,GTP酶激活蛋白I型GAP120和神经纤维瘤蛋白可能在RA诱导的神经母细胞瘤分化中具有效应功能。

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