Sandsmark D K, Pelletier C, Weber J D, Gutmann D H
Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Histol Histopathol. 2007 Aug;22(8):895-903. doi: 10.14670/HH-22.895.
The mammalian target of rapamycin (mTOR) is a highly conserved serine/threonine protein kinase that regulates a number of diverse biologic processes important for cell growth and proliferation, including ribosomal biogenesis and protein translation. In this regard, hyperactivation of the mTOR signaling pathway has been demonstrated in numerous human cancers, including a number of inherited cancer syndromes in which individuals have an increased risk of developing benign and malignant tumors. Three of these inherited cancer syndromes (Lhermitte-Duclos disease, neurofibromatosis type 1, and tuberous sclerosis complex) are characterized by significant central nervous system dysfunction and brain tumor formation. Each of these disorders is caused by a genetic mutation that disrupts the expression of proteins which negatively regulate mTOR signaling, indicating that the mTOR signaling pathway is critical for appropriate brain development and function. In this review, we discuss our current understanding of the mTOR signaling pathway and its role in promoting ribosome biogenesis and cell growth. We suggest that studies of this pathway may prove useful in identifying molecular targets for biologically-based therapies of brain tumors associated with these inherited cancer syndromes as well as sporadic central nervous system tumors.
雷帕霉素的哺乳动物靶点(mTOR)是一种高度保守的丝氨酸/苏氨酸蛋白激酶,它调节许多对细胞生长和增殖至关重要的不同生物学过程,包括核糖体生物合成和蛋白质翻译。在这方面,mTOR信号通路的过度激活已在许多人类癌症中得到证实,包括一些遗传性癌症综合征,其中个体患良性和恶性肿瘤的风险增加。这些遗传性癌症综合征中的三种(Lhermitte-Duclos病、1型神经纤维瘤病和结节性硬化症复合体)的特征是严重的中枢神经系统功能障碍和脑肿瘤形成。这些疾病中的每一种都是由基因突变引起的,该突变破坏了负调节mTOR信号的蛋白质的表达,表明mTOR信号通路对于适当的大脑发育和功能至关重要。在这篇综述中,我们讨论了我们目前对mTOR信号通路及其在促进核糖体生物合成和细胞生长中的作用的理解。我们认为,对该通路的研究可能有助于确定与这些遗传性癌症综合征相关的脑肿瘤以及散发性中枢神经系统肿瘤的基于生物学的治疗的分子靶点。