Guha A, Lau N, Huvar I, Gutmann D, Provias J, Pawson T, Boss G
Programme in Molecular Biology and Cancer, Samuel Lunenfeld Research Institute, Mt. Sinai Hospital, Toronto, Ontario, Canada.
Oncogene. 1996 Feb 1;12(3):507-13.
Neurofibromin, the gene product of NF1, is a Ras GTPase Activating Protein. The absence of neurofibromin leads to increased levels of Ras-GTP, which contributes to the proliferation of NF1 neurogenic sarcoma cell lines. Whether this pathogenic mechanism is applicable to benign and malignant peripheral nerve tumours from NF1 and non NF1 patients is not known, due to lack of a tissue based assay. We have adapted a colorimetric enzymatic assay for determining levels of Ras bound guanine nucleotides in tissues. Ras-GTP levels were increased in NF1 neurogenic sarcomas (15 times) and benign NF1 neurofibromas (four times), compared to non NF1 schwannomas. Neurofibromin was not expressed in NF1 sarcomas, in support of its important negative Ras regulatory role in the pathogenesis of NF1 peripheral nerve tumors.
神经纤维瘤蛋白是NF1的基因产物,是一种Ras鸟苷三磷酸酶激活蛋白。神经纤维瘤蛋白的缺失会导致Ras-GTP水平升高,这有助于NF1神经源性肉瘤细胞系的增殖。由于缺乏基于组织的检测方法,尚不清楚这种致病机制是否适用于NF1和非NF1患者的良性和恶性周围神经肿瘤。我们采用了一种比色酶法来测定组织中与Ras结合的鸟嘌呤核苷酸水平。与非NF1神经鞘瘤相比,NF1神经源性肉瘤(15倍)和良性NF1神经纤维瘤(4倍)中的Ras-GTP水平升高。NF1肉瘤中未表达神经纤维瘤蛋白,这支持了其在NF1周围神经肿瘤发病机制中对Ras的重要负调控作用。