Department of Biochemistry & Molecular Biology, Drexel University College of Medicine, Philadelphia, Pennsylvania, United States of America.
Cancer Signaling and Microenvironment Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States of America.
PLoS One. 2024 Jul 31;19(7):e0305121. doi: 10.1371/journal.pone.0305121. eCollection 2024.
Neurofibromatosis type 2 is a genetic disorder that results in the formation and progressive growth of schwannomas, ependymomas, and/or meningiomas. The NF2 gene encodes the Merlin protein, which links cell cortical elements to the actin cytoskeleton and regulates a number of key enzymes including Group I p21-activated kinases (PAKs), the Hippo-pathway kinase LATS, and mTORC. While PAK1 and PAK2 directly bind Merlin and transmit proliferation and survival signals when Merlin is mutated or absent, inhibition of Group 1 PAKs alone has not proven sufficient to completely stop the growth of NF2-deficient meningiomas or schwannomas in vivo, suggesting the need for a second pathway inhibitor. As the Hippo pathway is also activated in NF2-deficient cells, several inhibitors of the Hippo pathway have recently been developed in the form of YAP-TEAD binding inhibitors. These inhibitors prevent activation of pro-proliferation and anti-apoptotic Hippo pathway effectors. In this study, we show that PAK inhibition slows cell proliferation while TEAD inhibition promotes apoptotic cell death. Finally, we demonstrate the efficacy of PAK and TEAD inhibitor combinations in several NF2-deficient Schwannoma cell lines.
神经纤维瘤病 2 型是一种遗传性疾病,导致雪旺细胞瘤、室管膜瘤和/或脑膜瘤的形成和进行性生长。NF2 基因编码 Merlin 蛋白,该蛋白将细胞皮质元件连接到肌动蛋白细胞骨架,并调节许多关键酶,包括 Group I p21 激活激酶 (PAKs)、Hippo 通路激酶 LATS 和 mTORC。虽然 PAK1 和 PAK2 直接与 Merlin 结合,并在 Merlin 突变或缺失时传递增殖和存活信号,但单独抑制 Group 1 PAKs 不足以完全阻止 NF2 缺陷性脑膜瘤或雪旺细胞瘤在体内的生长,这表明需要第二种途径抑制剂。由于 Hippo 通路在 NF2 缺陷细胞中也被激活,最近已经开发出几种 Hippo 通路抑制剂,形式为 YAP-TEAD 结合抑制剂。这些抑制剂可防止促增殖和抗细胞凋亡 Hippo 通路效应物的激活。在这项研究中,我们表明 PAK 抑制减缓细胞增殖,而 TEAD 抑制促进细胞凋亡。最后,我们证明了 PAK 和 TEAD 抑制剂组合在几种 NF2 缺陷性 schwannoma 细胞系中的疗效。