Hilton David A, Shivane Aditya, Kirk Leanne, Bassiri Kayleigh, Enki Doyo G, Hanemann C Oliver
Department of Cellular and Anatomical Pathology, Derriford Hospital, Plymouth, UK.
Institute of Translational and Stratified Medicine, Plymouth University Peninsula Schools of Medicine & Dentistry, Plymouth, UK.
Neuropathology. 2016 Jun;36(3):250-61. doi: 10.1111/neup.12266. Epub 2015 Nov 10.
A minority of meningiomas are difficult to treat with surgery or radiotherapy, and chemotherapeutic alternatives are limited. This study aims to better understand pathways that are active in meningiomas, in order to direct future treatment strategies. We investigated the expression and activation of multiple growth factor receptors, their ligands and downstream signalling pathways in 30 meningiomas using immunohistochemistry. Expression was correlated with chromosome 22q loss. Membrane expression of VEGF receptor (VEGFR) and platelet-derived growth factor receptor (PDGFR)β was seen in 83% of tumors, Axl in 70%, EGFR in 50% and insulin-like growth factor receptor in 47%. Expression was similar in low- and high-grade tumors, but membrane EGFR expression was not seen in tumors showing chromosome 22q loss (P < 0.05). Expression of ligands (IGF, NRG, VEGF, Gas 6), and signalling proteins (Mek, Erk, Jnk, Akt) and pS6RP, was widespread. Western blot confirmed widespread Axl expression and supported selective expression of EGFR in NF2-intact meningiomas. The majority of meningiomas express and show activation of multiple growth factor receptors and their signalling pathways, irrespective of tumor grade. In addition to previously reported receptors, Axl offers a new therapeutic target. The findings also suggest that anti-EGFR based therapies may be less effective in meningiomas with 22q loss.
少数脑膜瘤难以通过手术或放疗进行治疗,且化疗选择有限。本研究旨在更好地了解脑膜瘤中活跃的信号通路,以指导未来的治疗策略。我们使用免疫组织化学方法研究了30例脑膜瘤中多种生长因子受体、其配体及下游信号通路的表达和激活情况。表达情况与22号染色体q臂缺失相关。83%的肿瘤可见血管内皮生长因子受体(VEGFR)和血小板衍生生长因子受体(PDGFR)β的膜表达,70%可见Axl表达,50%可见表皮生长因子受体(EGFR)表达,47%可见胰岛素样生长因子受体表达。低级别和高级别肿瘤中的表达情况相似,但在显示22号染色体q臂缺失的肿瘤中未见膜EGFR表达(P < 0.05)。配体(胰岛素样生长因子、神经调节蛋白、血管内皮生长因子、生长停滞特异性蛋白6)、信号蛋白(丝裂原活化蛋白激酶激酶、细胞外信号调节激酶、应激活化蛋白激酶、蛋白激酶B)和磷酸化核糖体蛋白S6的表达广泛。蛋白质印迹法证实了Axl的广泛表达,并支持EGFR在NF2基因完整的脑膜瘤中的选择性表达。大多数脑膜瘤表达并显示多种生长因子受体及其信号通路的激活,与肿瘤级别无关。除了先前报道的受体外,Axl提供了一个新的治疗靶点。研究结果还表明,基于抗EGFR的治疗在伴有22号染色体q臂缺失的脑膜瘤中可能效果较差。