Manchester Cancer Research Centre, Faculty of Biology, Medicine & Health, Division of Cancer Sciences, The University of Manchester, Manchester, UK.
Division of Molecular Pathology, The Institute of Cancer Research, London, UK.
Pigment Cell Melanoma Res. 2019 Mar;32(2):280-291. doi: 10.1111/pcmr.12741. Epub 2018 Oct 19.
The BRAF kinase and the MAPK pathway are targets of current melanoma therapies. However, MAPK pathway inhibition results in dynamic changes of downstream targets that can counteract inhibitor-action not only in during treatment, but also in acquired resistant tumours. One such dynamic change involves the expression of the transcription factor MITF, a crucial regulator of cell survival and proliferation in untreated as well as drug-addicted acquired resistant melanoma. Tight control over MITF expression levels is required for optimal melanoma growth, and while it is well established that the MAPK pathway regulates MITF expression, the actual mechanism is insufficiently understood. We reveal here, how BRAF through action on the transcription factors BRN2 and PAX3 executes control over the regulation of MITF expression in a manner that allows for considerable plasticity. This plasticity provides robustness to the BRAF mediated MITF regulation and explains the dynamics in MITF expression that are observed in patients in response to MAPK inhibitor therapy.
BRAF 激酶和 MAPK 通路是当前黑色素瘤治疗的靶点。然而,MAPK 通路抑制会导致下游靶标的动态变化,这些变化不仅会在治疗期间,而且会在获得性耐药肿瘤中对抗抑制剂的作用。这种动态变化之一涉及转录因子 MITF 的表达,MITF 是未治疗和药物成瘾性获得性耐药黑色素瘤中细胞存活和增殖的关键调节剂。MITF 表达水平的严格控制是黑色素瘤最佳生长所必需的,虽然已经确定 MAPK 通路调节 MITF 的表达,但实际机制还不够了解。我们在这里揭示了 BRAF 通过作用于转录因子 BRN2 和 PAX3,以允许相当大的可塑性的方式对 MITF 表达的调节进行控制。这种可塑性为 BRAF 介导的 MITF 调节提供了稳健性,并解释了在接受 MAPK 抑制剂治疗的患者中观察到的 MITF 表达的动态变化。