Department of Circulation and Medical Imaging, Faculty of Medicine, Norwegian University of Science and Technology, P.O. Box 8905, 7491 Trondheim, Norway.
Center for Oral Health Services and Research (TkMidt), 7030 Trondheim, Norway.
Int J Mol Sci. 2019 Sep 27;20(19):4800. doi: 10.3390/ijms20194800.
Metastatic disease is the leading cause of death in breast cancer patients. Disrupting the cancer cell's ability to migrate may be a strategy for hindering metastasis. Cytosolic phospholipase A2 α (cPLA2α), along with downstream proinflammatory and promigratory metabolites, has been implicated in several aspects of tumorigenesis, as well as metastasis, in various types of cancer. In this study, we aim to characterize the response to reduced cPLA2α activity in metastatic versus non-metastatic cells. We employ an isogenic murine cell line pair displaying metastatic (4T1) and non-metastatic (67NR) phenotype to investigate the role of cPLA2α on migration. Furthermore, we elucidate the effect of reduced cPLA2α activity on global gene expression in the metastatic cell line. Enzyme inhibition is achieved by using a competitive pharmacological inhibitor, cPLA2α inhibitor X (CIX). Our data show that 4T1 expresses significantly higher cPLA2α levels as compared to 67NR, and the two cell lines show different sensitivity to the CIX treatment with regards to metabolism and proliferation. Inhibition of cPLA2α at nontoxic concentrations attenuates migration of highly metastatic 4T1 cells, but not non-metastatic 67NR cells. Gene expression analysis indicates that processes such as interferon type I (IFN-I) signaling and cell cycle regulation are key processes regulated by cPLA2a in metastatic 4T1 cells, supporting the findings from the biological assays. This study demonstrates that two isogenic cancer cell lines with different metastatic potential respond differently to reduced cPLA2α activity. In conclusion, we argue that cPLA2α is a potential therapeutic target in cancer and that enzyme inhibition may inhibit metastasis through an anti-migratory mechanism, possibly involving Toll-like receptor signaling and type I interferons.
转移性疾病是乳腺癌患者死亡的主要原因。破坏癌细胞的迁移能力可能是阻止转移的一种策略。细胞质型磷脂酶 A2α(cPLA2α)及其下游促炎和促迁移代谢物已被涉及多种癌症的肿瘤发生和转移的多个方面。在这项研究中,我们旨在描述对转移性和非转移性细胞中 cPLA2α 活性降低的反应。我们使用具有转移性(4T1)和非转移性(67NR)表型的同基因鼠细胞系对来研究 cPLA2α 对迁移的作用。此外,我们阐明了降低 cPLA2α 活性对转移性细胞系中全局基因表达的影响。酶抑制是通过使用竞争性药理抑制剂 cPLA2α 抑制剂 X(CIX)来实现的。我们的数据表明,与 67NR 相比,4T1 表达的 cPLA2α 水平明显更高,并且这两种细胞系在代谢和增殖方面对 CIX 处理的敏感性不同。在非毒性浓度下抑制 cPLA2α 可减弱高度转移性 4T1 细胞的迁移,但不能减弱非转移性 67NR 细胞的迁移。基因表达分析表明,干扰素 I 型(IFN-I)信号和细胞周期调节等过程是 cPLA2a 在转移性 4T1 细胞中调节的关键过程,这支持了生物学测定的结果。这项研究表明,两种具有不同转移潜能的同基因癌细胞系对降低 cPLA2α 活性的反应不同。总之,我们认为 cPLA2α 是癌症的潜在治疗靶标,并且酶抑制可能通过抗迁移机制抑制转移,可能涉及 Toll 样受体信号和 I 型干扰素。