Heiland Dieter Henrik, Haaker Gerrit, Delev Daniel, Mercas Bianca, Masalha Waseem, Heynckes Sabrina, Gäbelein Annette, Pfeifer Dietmar, Carro Maria Stella, Weyerbrock Astrid, Prinz Marco, Schnell Oliver
Department of Neurosurgery, Medical Center - University of Freiburg, Germany.
Faculty of Medicine, University of Freiburg, Germany.
Oncotarget. 2017 Jun 27;8(26):42214-42225. doi: 10.18632/oncotarget.15031.
Glioblastoma multiforme are highly malignant brain tumours with frequent genetic and epigenetic alterations. The poor clinical outcome of these tumours necessitates the development of new treatment options. Immunotherapies for glioblastoma multiforme including PD1/PD-L1 inhibition are currently tested in ongoing clinical trials. The purpose of this study was to investigate the molecular background of PD-L1 expression in glioblastoma multiforme and to find associated pathway activation and genetic alterations. We show that PD-L1 is up-regulated in IDH1/2 wildtype glioblastoma multiforme compared to lower-grade gliomas. In addition, a strong association of PD-L1 with the mesenchymal expression subgroup was observed. Consistent with that, NF1 mutation and corresponding activation of the MAPK pathway was strongly connected to PD-L1 expression. Our findings may explain different response to PD-L1 inhibition of patients in ongoing trials and may help to select patients that may profit of immunotherapy in the future.
多形性胶质母细胞瘤是高度恶性的脑肿瘤,常有基因和表观遗传改变。这些肿瘤较差的临床结果使得开发新的治疗方案成为必要。包括PD1/PD-L1抑制在内的多形性胶质母细胞瘤免疫疗法目前正在进行临床试验测试。本研究的目的是调查多形性胶质母细胞瘤中PD-L1表达的分子背景,并找出相关的信号通路激活和基因改变。我们发现,与低级别胶质瘤相比,IDH1/2野生型多形性胶质母细胞瘤中PD-L1表达上调。此外,观察到PD-L1与间充质表达亚组有很强的关联。与此一致的是,NF1突变和相应的MAPK信号通路激活与PD-L1表达密切相关。我们的研究结果可能解释了正在进行的试验中患者对PD-L1抑制的不同反应,并可能有助于选择未来可能从免疫治疗中获益的患者。