Gomez-Cambronero Julian, Fite Kristen, Miller Taylor E
Wright State University School of Medicine, Department of Biochemistry and Molecular Biology, 3640 Colonel Glenn Highway, Dayton, OH 45435, USA.
Wright State University School of Medicine, Department of Biochemistry and Molecular Biology, 3640 Colonel Glenn Highway, Dayton, OH 45435, USA.
Adv Biol Regul. 2018 May;68:107-119. doi: 10.1016/j.jbior.2017.08.002. Epub 2017 Aug 24.
Phospholipase D (PLD) plays a key role in both cell membrane lipid reorganization and architecture, as well as a cell signaling protein via the product of its enzymatic reaction, phosphatidic acid (PA). PLD is involved in promoting breast cancer cell growth, proliferation, and metastasis and both gene and protein expression are upregulated in breast carcinoma human samples. In spite of all this, the ultimate reason as to why PLD expression is high in cancer cells vs. their normal counterparts remains largely unknown. Until we understand this and the associated signaling pathways, it will be difficult to establish PLD as a bona fide target to explore new potential cancer therapeutic approaches. Recently, our lab has identified several molecular mechanisms by which PLD expression is high in breast cancer cells and they all involve post-transcriptional control of its mRNA. First, PA, a mitogen, functions as a protein and mRNA stabilizer that counteracts natural decay and degradation. Second, there is a repertoire of microRNAs (miRs) that keep PLD mRNA translation at low levels in normal cells, but their effects change with starvation and during endothelial-to-mesenchymal transition (EMT) in cancer cells. Third, there is a novel way of post-transcriptional regulation of PLD involving 3'-exonucleases, specifically the deadenylase, Poly(A)-specific Ribonuclease (PARN), which tags mRNA for mRNA for degradation. This would enable PLD accumulation and ultimately breast cancer cell growth. We review in depth the emerging field of post-transcriptional regulation of PLD, which is only recently beginning to be understood. Since, surprisingly, so little is known about post-transcriptional regulation of PLD and related phospholipases (PLC or PLA), this new knowledge could help our understanding of how post-transcriptional deregulation of a lipid enzyme expression impacts tumor growth.
磷脂酶D(PLD)在细胞膜脂质重组和结构形成中发挥关键作用,同时作为一种细胞信号蛋白,通过其酶促反应产物磷脂酸(PA)发挥作用。PLD参与促进乳腺癌细胞的生长、增殖和转移,在人类乳腺癌样本中,其基因和蛋白表达均上调。尽管如此,与正常细胞相比,癌细胞中PLD表达高的根本原因在很大程度上仍不清楚。在我们理解这一点以及相关信号通路之前,将PLD确立为探索新的潜在癌症治疗方法的真正靶点将很困难。最近,我们实验室已经确定了几种分子机制,通过这些机制,乳腺癌细胞中PLD表达较高,且这些机制均涉及对其mRNA的转录后调控。首先,作为一种有丝分裂原的PA,起到蛋白质和mRNA稳定剂的作用,可抵消自然衰变和降解。其次,有一系列微小RNA(miRs)在正常细胞中将PLD mRNA翻译维持在低水平,但在饥饿期间以及癌细胞的内皮-间充质转化(EMT)过程中,它们的作用会发生变化。第三,存在一种新的PLD转录后调控方式,涉及3'-核酸外切酶,特别是去腺苷酸化酶聚腺苷酸特异性核糖核酸酶(PARN),它标记mRNA以便降解。这将导致PLD积累并最终促进乳腺癌细胞生长。我们深入综述了PLD转录后调控这一新兴领域,该领域直到最近才开始被理解。令人惊讶的是,由于对PLD及相关磷脂酶(PLC或PLA)的转录后调控了解甚少,这一新知识有助于我们理解脂质酶表达的转录后失调如何影响肿瘤生长。