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糖酵解酶在细胞死亡中的调节作用。

Modulatory roles of glycolytic enzymes in cell death.

机构信息

Laboratoire de Biologie Moléculaire et Cellulaire de Cancer, Hôpital Kirchberg, 9, rue Edward Steichen, L-2540 Luxembourg, Luxembourg.

Department of Pharmacy, College of Pharmacy, Seoul National University, Seoul 151-742, Republic of Korea.

出版信息

Biochem Pharmacol. 2014 Nov 1;92(1):22-30. doi: 10.1016/j.bcp.2014.07.005. Epub 2014 Jul 15.

Abstract

Cancer cells depend on an altered energy metabolism characterized by increased rates of both glycolysis and glutaminolysis. Accordingly, corresponding key metabolic enzymes are overexpressed or hyperactivated. As a result, this newly acquired metabolic profile determines most other cancer hallmarks including resistance to cell death. Recent findings highlighted metabolic enzymes as direct modulators of cell death pathways. Conversely, key mediators of cell death mechanisms are emerging as new binding partners of glycolytic actors; moreover, there is evidence that metabolic regulators re-localize to specific subcellular compartments or organelles to modulate various types of cell demise. The final outcome is the resistance against cell death programs. Current findings give a new meaning to metabolic pathways and allow understanding how they affect cancer-specific pathological alterations. Furthermore, they shed light on potentially targetable functions of metabolic actors to restore susceptibility of cancer cells to death. Here, we discuss an emerging interplay between cell metabolism and cell death, focusing on interactions that may offer new options of targeted therapies in cancer treatment involving more specifically hexokinases and glyceraldehyde-3-phosphate dehydrogenase.

摘要

癌细胞依赖于一种改变了的能量代谢,其特征是糖酵解和谷氨酰胺分解的速率增加。相应地,相应的关键代谢酶被过度表达或过度激活。因此,这种新获得的代谢特征决定了大多数其他癌症特征,包括对细胞死亡的抵抗。最近的发现强调了代谢酶作为细胞死亡途径的直接调节剂。相反,细胞死亡机制的关键介质正在成为糖酵解因子的新结合伙伴;此外,有证据表明代谢调节剂重新定位到特定的亚细胞区室或细胞器,以调节各种类型的细胞死亡。最终结果是对细胞死亡程序的抵抗。目前的发现赋予了代谢途径新的意义,并使人们能够理解它们如何影响癌症特有的病理改变。此外,它们揭示了代谢因子潜在的可靶向功能,以恢复癌细胞对死亡的敏感性。在这里,我们讨论细胞代谢和细胞死亡之间新出现的相互作用,重点讨论可能为癌症治疗中的靶向治疗提供新选择的相互作用,更具体地涉及己糖激酶和甘油醛-3-磷酸脱氢酶。

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