Cristea Sandra, Sage Julien
Department of Pediatrics, Stanford University, Stanford, California; Department of Genetics, Stanford University, Stanford, California.
Department of Pediatrics, Stanford University, Stanford, California; Department of Genetics, Stanford University, Stanford, California.
J Thorac Oncol. 2016 Aug;11(8):1233-1241. doi: 10.1016/j.jtho.2016.04.018. Epub 2016 Apr 29.
The activity of the RAF/MEK/ERK signaling pathway is critical for the proliferation of normal and cancerous cells. Oncogenic mutations driving the development of lung adenocarcinoma often activate this signaling pathway. In contrast, pathway activity levels and their biological roles are not well established in small cell lung cancer (SCLC), a fast-growing neuroendocrine lung cancer subtype. Here we discuss the function of the RAF/MEK/ERK kinase pathway and the mechanisms leading to its activation in SCLC cells. In particular, we argue that activation of this pathway may be beneficial to the survival, proliferation, and spread of SCLC cells in response to multiple stimuli. We also consider evidence that high levels of RAF/MEK/ERK pathway activity may be detrimental to SCLC tumors, including in part by interfering with their neuroendocrine fate. On the basis of these observations, we examined when small molecules targeting kinases in the RAF/MEK/ERK pathway may be useful therapeutically in patients with SCLC, including in combination with other therapeutic agents.
RAF/MEK/ERK信号通路的活性对于正常细胞和癌细胞的增殖至关重要。驱动肺腺癌发展的致癌突变常常激活该信号通路。相比之下,在小细胞肺癌(SCLC)这一快速生长的神经内分泌肺癌亚型中,该信号通路的活性水平及其生物学作用尚未完全明确。在此,我们讨论RAF/MEK/ERK激酶信号通路在SCLC细胞中的功能以及导致其激活的机制。特别地,我们认为该信号通路的激活可能有利于SCLC细胞在多种刺激下的存活、增殖和扩散。我们还考虑了相关证据,即高水平的RAF/MEK/ERK信号通路活性可能对SCLC肿瘤有害,部分原因是干扰了它们的神经内分泌命运。基于这些观察结果,我们研究了靶向RAF/MEK/ERK信号通路中激酶的小分子何时可能在SCLC患者的治疗中发挥作用,包括与其他治疗药物联合使用时。