Department of Pediatrics, Stanford University, Stanford, California.
Department of Genetics, Stanford University, Stanford, California.
Cancer Res. 2020 Mar 15;80(6):1293-1303. doi: 10.1158/0008-5472.CAN-19-1027. Epub 2020 Jan 22.
Small-cell lung cancer (SCLC) is an aggressive form of lung cancer with dismal survival rates. While kinases often play key roles driving tumorigenesis, there are strikingly few kinases known to promote the development of SCLC. Here, we investigated the contribution of the MAPK module MEK5-ERK5 to SCLC growth. MEK5 and ERK5 were required for optimal survival and expansion of SCLC cell lines and . Transcriptomics analyses identified a role for the MEK5-ERK5 axis in the metabolism of SCLC cells, including lipid metabolism. In-depth lipidomics analyses showed that loss of MEK5/ERK5 perturbs several lipid metabolism pathways, including the mevalonate pathway that controls cholesterol synthesis. Notably, depletion of MEK5/ERK5 sensitized SCLC cells to pharmacologic inhibition of the mevalonate pathway by statins. These data identify a new MEK5-ERK5-lipid metabolism axis that promotes the growth of SCLC. SIGNIFICANCE: This study is the first to investigate MEK5 and ERK5 in SCLC, linking the activity of these two kinases to the control of cell survival and lipid metabolism.
小细胞肺癌(SCLC)是一种侵袭性肺癌,患者生存率极低。尽管激酶通常在推动肿瘤发生中起着关键作用,但已知能够促进 SCLC 发展的激酶却寥寥无几。在这里,我们研究了 MAPK 模块 MEK5-ERK5 对 SCLC 生长的贡献。MEK5 和 ERK5 是 SCLC 细胞系最佳存活和扩增所必需的。转录组学分析确定了 MEK5-ERK5 轴在 SCLC 细胞代谢中的作用,包括脂质代谢。深入的脂质组学分析表明,MEK5/ERK5 的缺失会破坏几种脂质代谢途径,包括控制胆固醇合成的甲羟戊酸途径。值得注意的是,MEK5/ERK5 的耗竭使 SCLC 细胞对他汀类药物抑制甲羟戊酸途径的药理抑制作用更为敏感。这些数据确定了一个新的 MEK5-ERK5-脂质代谢轴,促进了 SCLC 的生长。意义:这项研究首次在 SCLC 中研究了 MEK5 和 ERK5,将这两种激酶的活性与细胞存活和脂质代谢的控制联系起来。