Gupta Preeti, Taiyab Aaliya, Hussain Afzal, Alajmi Mohamed F, Islam Asimul, Hassan Md Imtaiyaz
Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, Jamia Nagar, New Delhi 110025, India.
Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Cancers (Basel). 2021 Apr 15;13(8):1898. doi: 10.3390/cancers13081898.
Sphingolipid metabolites have emerged as critical players in the regulation of various physiological processes. Ceramide and sphingosine induce cell growth arrest and apoptosis, whereas sphingosine-1-phosphate (S1P) promotes cell proliferation and survival. Here, we present an overview of sphingolipid metabolism and the compartmentalization of various sphingolipid metabolites. In addition, the sphingolipid rheostat, a fine metabolic balance between ceramide and S1P, is discussed. Sphingosine kinase (SphK) catalyzes the synthesis of S1P from sphingosine and modulates several cellular processes and is found to be essentially involved in various pathophysiological conditions. The regulation and biological functions of SphK isoforms are discussed. The functions of S1P, along with its receptors, are further highlighted. The up-regulation of SphK is observed in various cancer types and is also linked to radio- and chemoresistance and poor prognosis in cancer patients. Implications of the SphK/S1P signaling axis in human pathologies and its inhibition are discussed in detail. Overall, this review highlights current findings on the SphK/S1P signaling axis from multiple angles, including their functional role, mechanism of activation, involvement in various human malignancies, and inhibitor molecules that may be used in cancer therapy.
鞘脂代谢产物已成为各种生理过程调节中的关键参与者。神经酰胺和鞘氨醇可诱导细胞生长停滞和凋亡,而1-磷酸鞘氨醇(S1P)则促进细胞增殖和存活。在此,我们概述了鞘脂代谢以及各种鞘脂代谢产物的区室化。此外,还讨论了鞘脂变阻器,即神经酰胺和S1P之间精细的代谢平衡。鞘氨醇激酶(SphK)催化由鞘氨醇合成S1P,并调节多种细胞过程,且发现其在各种病理生理状况中发挥重要作用。本文讨论了SphK亚型的调节及其生物学功能。进一步强调了S1P及其受体的功能。在各种癌症类型中均观察到SphK的上调,并且其还与癌症患者的放疗和化疗耐药性以及不良预后相关。详细讨论了SphK/S1P信号轴在人类疾病中的意义及其抑制作用。总体而言,本综述从多个角度突出了关于SphK/S1P信号轴的当前研究结果,包括它们的功能作用、激活机制、在各种人类恶性肿瘤中的参与情况以及可能用于癌症治疗的抑制剂分子。