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磷脂酶C在细胞侵袭和转移中的作用。

Role of phospholipase C in cell invasion and metastasis.

作者信息

Lattanzio Rossano, Piantelli Mauro, Falasca Marco

机构信息

Aging Research Centre, G. d'Annunzio University Foundation, 66013 Chieti, Italy.

出版信息

Adv Biol Regul. 2013 Sep;53(3):309-18. doi: 10.1016/j.jbior.2013.07.006. Epub 2013 Jul 18.

Abstract

Phospholipases are enzymes that use phospholipids as substrate and are classified in three major classes A, C and D based on the reaction they catalyse. Phosphatidylinositol-specific Phospholipase C enzymes utilize phosphatidylinositol 4,5-bisphosphate as substrate and cleave the bond between the glycerol and the phosphate to produce important second messenger such as inositol trisphosphate and diacylglycerol. The Phospholipase C members are the most well-known phospholipases for their role in lipid signalling and cell proliferation and comprise 13 isoforms classified in 6 distinct sub-families. In particular, signalling activated by Phospholipase C γ, mostly activated by receptor and non-receptor tyrosine kinases, is well characterized in different cell systems. Increasing evidence suggest that Phospholipase C γ plays a key role in cell migration and invasion. Because of its role in cell growth and invasion, aberrant Phospholipase C γ signalling can contribute to carcinogenesis. A major challenge facing investigators who seek to target Phospholipase C γ directly is the fact that it is considered an "undruggable" protein. Indeed, isoform specificity and toxicity represents a big hurdle in the development of Phospholipase C γ small molecule inhibitors. Therefore, a future development in the field could be the identification of interacting partners as therapeutic targets that could be more druggable than Phospholipase C γ.

摘要

磷脂酶是以磷脂为底物的酶,根据它们催化的反应可分为A、C和D三大类。磷脂酰肌醇特异性磷脂酶C以磷脂酰肌醇4,5-二磷酸为底物,裂解甘油和磷酸之间的键,产生重要的第二信使,如肌醇三磷酸和二酰基甘油。磷脂酶C成员因其在脂质信号传导和细胞增殖中的作用而成为最著名的磷脂酶,包括13种亚型,分为6个不同的亚家族。特别是,由磷脂酶Cγ激活的信号传导,主要由受体和非受体酪氨酸激酶激活,在不同的细胞系统中已得到充分表征。越来越多的证据表明,磷脂酶Cγ在细胞迁移和侵袭中起关键作用。由于其在细胞生长和侵袭中的作用,异常的磷脂酶Cγ信号传导可能导致癌症发生。试图直接靶向磷脂酶Cγ的研究人员面临的一个主要挑战是,它被认为是一种“不可成药”的蛋白质。事实上,亚型特异性和毒性是磷脂酶Cγ小分子抑制剂开发中的一大障碍。因此,该领域未来的发展可能是确定相互作用的伙伴作为治疗靶点,这些靶点可能比磷脂酶Cγ更具可成药性。

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