Galadari Sehamuddin, Rahman Anees, Pallichankandy Siraj, Thayyullathil Faisal
Cell Signaling Laboratory, Department of Biochemistry, College of Medicine and Health Sciences, UAE University, Al Ain, PO Box 17666, Abu Dhabi, United Arab Emirates,
Apoptosis. 2015 May;20(5):689-711. doi: 10.1007/s10495-015-1109-1.
Studies over the past two decades have identified ceramide as a multifunctional central molecule in the sphingolipid biosynthetic pathway. Given its diverse tumor suppressive activities, molecular understanding of ceramide action will produce fundamental insights into processes that limit tumorigenesis and may identify key molecular targets for therapeutic intervention. Ceramide can be activated by a diverse array of stresses such as heat shock, genotoxic damage, oxidative stress and anticancer drugs. Ceramide triggers a variety of tumor suppressive and anti-proliferative cellular programs such as apoptosis, autophagy, senescence, and necroptosis by activating or repressing key effector molecules. Defects in ceramide generation and metabolism in cancer contribute to tumor cell survival and resistance to chemotherapy. The potent and versatile anticancer activity profile of ceramide has motivated drug development efforts to (re-)activate ceramide in established tumors. This review focuses on our current understanding of the tumor suppressive functions of ceramide and highlights the potential downstream targets of ceramide which are involved in its tumor suppressive action.
过去二十年的研究已确定神经酰胺是鞘脂生物合成途径中的多功能核心分子。鉴于其多样的肿瘤抑制活性,对神经酰胺作用的分子理解将为限制肿瘤发生的过程提供基本见解,并可能确定治疗干预的关键分子靶点。神经酰胺可被多种应激激活,如热休克、基因毒性损伤、氧化应激和抗癌药物。神经酰胺通过激活或抑制关键效应分子触发多种肿瘤抑制和抗增殖细胞程序,如凋亡、自噬、衰老和坏死性凋亡。癌症中神经酰胺生成和代谢的缺陷有助于肿瘤细胞存活和对化疗的耐药性。神经酰胺强大而多样的抗癌活性促使人们努力开发药物以在已形成的肿瘤中(重新)激活神经酰胺。本综述重点关注我们目前对神经酰胺肿瘤抑制功能的理解,并强调参与其肿瘤抑制作用的神经酰胺潜在下游靶点。