Center for the Study of Systems Biology, School of Biological Sciences, Georgia Institute of Technology, 950 Atlantic Drive, NW, Atlanta, Georgia, 30332, United States.
Department of BioSciences, Rice University, Houston, Texas, 77005, United States.
Sci Rep. 2020 Apr 9;10(1):6140. doi: 10.1038/s41598-020-63061-0.
Diffuse intrinsic pontine glioma (DIPG) is a lethal pediatric brain cancer whose median survival time is under one year. The possible roles of the two most common DIPG associated cytoplasmic ACVR1 receptor kinase domain mutants, G328V and R206H, are reexamined in the context of new biochemical results regarding their intrinsic relative ATPase activities. At 37 °C, the G328V mutant displays a 1.8-fold increase in intrinsic kinase activity over wild-type, whereas the R206H mutant shows similar activity. The higher G328V mutant intrinsic kinase activity is consistent with the statistically significant longer overall survival times of DIPG patients harboring ACVR1 G328V tumors. Based on the potential cross-talk between ACVR1 and TβRI pathways and known and predicted off-targets of ACVR1 inhibitors, we further validated the inhibition effects of several TβRI inhibitors on ACVR1 wild-type and G328V mutant patient tumor derived DIPG cell lines at 20-50 µM doses. SU-DIPG-IV cells harboring the histone H3.1K27M and activating ACVR1 G328V mutations appeared to be less susceptible to TβRI inhibition than SF8628 cells harboring the H3.3K27M mutation and wild-type ACVR1. Thus, inhibition of hidden oncogenic signaling pathways in DIPG such as TβRI that are not limited to ACVR1 itself may provide alternative entry points for DIPG therapeutics.
弥漫性内在脑桥神经胶质瘤(DIPG)是一种致命的儿童脑癌,中位生存时间不到一年。在新的生化结果的背景下,重新研究了与两种最常见的 DIPG 相关的细胞质 ACVR1 受体激酶结构域突变体(G328V 和 R206H)的可能作用,这些结果涉及它们的内在相对 ATP 酶活性。在 37°C 下,G328V 突变体的内在激酶活性比野生型增加了 1.8 倍,而 R206H 突变体显示出相似的活性。较高的 G328V 突变体内在激酶活性与 DIPG 患者中携带 ACVR1 G328V 肿瘤的总生存时间明显延长一致。基于 ACVR1 和 TβRI 途径之间的潜在串扰以及已知和预测的 ACVR1 抑制剂的脱靶效应,我们进一步验证了几种 TβRI 抑制剂在 20-50µM 剂量下对携带 ACVR1 野生型和 G328V 突变的患者来源 DIPG 细胞系的抑制作用。与携带 H3.3K27M 突变和野生型 ACVR1 的 SF8628 细胞相比,携带组蛋白 H3.1K27M 和激活的 ACVR1 G328V 突变的 SU-DIPG-IV 细胞似乎对 TβRI 抑制的敏感性较低。因此,抑制 DIPG 中的隐藏致癌信号通路,如不限于 ACVR1 本身的 TβRI,可能为 DIPG 治疗提供替代切入点。