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Lysophosphatidic acid production and action: critical new players in breast cancer initiation and progression

机译:溶血磷脂酸的产生和作用:乳腺癌发生和发展的关键新参与者

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摘要

Lysophosphatidic acid (LPA) is a potent lipid mediator that acts on a series of specific G protein-coupled receptors, leading to diverse biological actions. Lysophosphatidic acid induces cell proliferation, survival and migration, which are critically required for tumour formation and metastasis. This bioactive lipid is produced by the ectoenzyme lysophospholipase D or autotaxin (ATX), earlier known as an autocrine motility factor. The ATX–LPA signalling axis has emerged as an important player in many types of cancer. Indeed, aberrant expression of ATX and LPA receptors occurs during the development and progression of breast cancer. Importantly, expression of either ATX or LPA receptors in the mammary gland of transgenic mice is sufficient to induce the development of a high frequency of invasive and metastatic mammary cancers. The focus of research now turns to understanding the mechanisms by which ATX and LPA promote mammary tumourigenesis and metastasis. Targeting the ATX–LPA signalling axis for drug development may further improve outcomes in patients with breast cancer.
机译:溶血磷脂酸(LPA)是一种有效的脂质介体,作用于一系列特定的G蛋白偶联受体,从而导致多种生物学作用。溶血磷脂酸诱导细胞增殖,存活和迁移,这对于肿瘤形成和转移是至关重要的。这种具有生物活性的脂质是由外部酶溶血磷脂酶D或自分泌生物素(ATX)(先前称为自分泌运动因子)产生的。 ATX-LPA信号轴已经成为许多类型癌症中的重要角色。实际上,ATX和LPA受体的异常表达发生在乳腺癌的发生和发展过程中。重要的是,ATX或LPA受体在转基因小鼠乳腺中的表达足以诱导高频率的侵袭性和转移性乳癌的发展。现在的研究重点转向了解ATX和LPA促进乳腺肿瘤发生和转移的机制。以ATX-LPA信号转导轴为药物开发靶点可能会进一步改善乳腺癌患者的预后。

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