Department of Clinical and Molecular Medicine, Sapienza University of Rome, 00185 Rome, Italy.
Hematology, "Sant' Andrea" University Hospital, Sapienza University of Rome, 00185 Rome, Italy.
Cells. 2020 Feb 11;9(2):404. doi: 10.3390/cells9020404.
Neoplastic cells rewire their metabolism, acquiring a selective advantage over normal cells and a protection from therapeutic agents. The mammalian Target of Rapamycin (mTOR) is a serine/threonine kinase involved in a variety of cellular activities, including the control of metabolic processes. mTOR is hyperactivated in a large number of tumor types, and among them, in many hematologic malignancies. In this article, we summarized the evidence from the literature that describes a central role for mTOR in the acquisition of new metabolic phenotypes for different hematologic malignancies, in concert with other metabolic modulators (AMPK, HIF1α) and microenvironmental stimuli, and shows how these features can be targeted for therapeutic purposes.
肿瘤细胞重新布线其代谢,相较于正常细胞获得选择性优势,并对治疗药物产生保护。哺乳动物雷帕霉素靶蛋白(mTOR)是一种丝氨酸/苏氨酸激酶,参与多种细胞活动,包括代谢过程的控制。mTOR 在大量肿瘤类型中过度激活,其中包括许多血液系统恶性肿瘤。在本文中,我们总结了文献中的证据,这些证据描述了 mTOR 在不同血液系统恶性肿瘤获得新的代谢表型方面的核心作用,与其他代谢调节剂(AMPK、HIF1α)和微环境刺激协同作用,并展示了如何针对这些特征进行治疗。