Fu Weijia, Hou Xue, Dong Lihua, Hou Wei
Department of Radiation Oncology & Therapy, The First Hospital of Jilin University, Changchun, China.
Jilin Provincial Key Laboratory of Radiation Oncology & Therapy, The First Hospital of Jilin University, Changchun, China.
Front Cell Dev Biol. 2023 Feb 27;11:1098482. doi: 10.3389/fcell.2023.1098482. eCollection 2023.
Glioblastoma (GBM) is the most malignant of astrocytomas mainly involving the cerebral hemispheres and the cerebral cortex. It is one of the fatal and refractory solid tumors, with a 5-year survival rate of merely 5% among the adults. IL6/JAK/STAT3 is an important signaling pathway involved in the pathogenesis and progression of GBM. The expression of STAT3 in GBM tissues is substantially higher than that of normal brain cells. The abnormal activation of STAT3 renders the tumor microenvironment of GBM immunosuppression. Besides, blocking the STAT3 pathway can effectively inhibit the growth and metastasis of GBM. On this basis, inhibition of STAT3 may be a new therapeutic approach for GBM, and the combination of STAT3 targeted therapy and conventional therapies may improve the current status of GBM treatment. This review summarized the roles of STAT3 in the pathogenesis of GBM and the feasibility of STAT3 for GBM target therapy.
胶质母细胞瘤(GBM)是星形细胞瘤中最恶性的一种,主要累及大脑半球和大脑皮层。它是致命且难治的实体瘤之一,在成年人中的5年生存率仅为5%。白细胞介素6/Janus激酶/信号转导子和转录激活子3(IL6/JAK/STAT3)是参与GBM发病机制和进展的重要信号通路。STAT3在GBM组织中的表达明显高于正常脑细胞。STAT3的异常激活导致GBM的肿瘤微环境发生免疫抑制。此外,阻断STAT3通路可有效抑制GBM的生长和转移。在此基础上,抑制STAT3可能是GBM的一种新治疗方法,STAT3靶向治疗与传统治疗相结合可能改善GBM的治疗现状。本文综述了STAT3在GBM发病机制中的作用以及STAT3用于GBM靶向治疗的可行性。