Haga Arayo, Nagai Hiroyuki, Deyashiki Yoshihiro
Gifu Prefectural Research Institute for Health and Environmental Science, Naka-Fudougaoka, Kakamigahara, Japan.
Cancer Invest. 2009 May;27(4):384-90. doi: 10.1080/07357900802491469.
Autotaxin (ATX) is an approximately 125-kDa transmembrane protein that is considered to be a tumor progression factor based on its lysophospholipase D activity. Here, we report that lysophosphatidic acid produced by ATX promotes the secretion of matrix metalloproteinase-3 (MMP3) from the human fibrosarcoma cell line HT-1080. The c-Jun N-terminal kinases (JNKs) and c-Jun of HT-1080 cells were rapidly phosphorylated after ATX treatment. A specific JNK inhibitor also exhibited this activation of signaling molecules and MMP3 expression. The present results suggest a novel function of ATX in promoting MMP3 production via the mitogen-activated protein kinase cascade, thereby stimulating tumor cell invasiveness.
自分泌运动因子(ATX)是一种分子量约为125 kDa的跨膜蛋白,基于其溶血磷脂酶D活性,它被认为是一种肿瘤进展因子。在此,我们报告ATX产生的溶血磷脂酸可促进人纤维肉瘤细胞系HT - 1080分泌基质金属蛋白酶-3(MMP3)。用ATX处理后,HT - 1080细胞的c - Jun氨基末端激酶(JNKs)和c - Jun迅速被磷酸化。一种特异性JNK抑制剂也表现出这种信号分子的激活和MMP3表达。目前的结果表明,ATX具有一种新功能,即通过丝裂原活化蛋白激酶级联反应促进MMP3的产生,从而刺激肿瘤细胞的侵袭性。