Liu Xiaojin, Liu Yuan, Qi Yiwei, Huang Yimin, Hu Feng, Dong Fangyong, Shu Kai, Lei Ting
Sino-German Neuro-Oncology Molecular Laboratory, Department of Neurosurgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Front Oncol. 2022 May 4;12:822085. doi: 10.3389/fonc.2022.822085. eCollection 2022.
It is commonly recognized, that glioblastoma is a large complex composed of neoplastic and non-neoplastic cells. Tumor-associated macrophages account for the majority of tumor bulk and play pivotal roles in tumor proliferation, migration, invasion, and survival. There are sophisticated interactions between malignant cells and tumor associated-macrophages. Tumor cells release a variety of chemokines, cytokines, and growth factors that subsequently lead to the recruitment of TAMs, which in return released a plethora of factors to construct an immunosuppressive and tumor-supportive microenvironment. In this article, we have reviewed the biological characteristics of glioblastoma-associated macrophages and microglia, highlighting the emerging molecular targets and related signal pathways involved in the interaction between TAMs and glioblastoma cells, as well as the potential TAMs-associated therapeutic targets for glioblastoma.
人们普遍认识到,胶质母细胞瘤是一个由肿瘤细胞和非肿瘤细胞组成的大型复合体。肿瘤相关巨噬细胞占肿瘤大部分体积,并在肿瘤增殖、迁移、侵袭和存活中起关键作用。恶性细胞与肿瘤相关巨噬细胞之间存在复杂的相互作用。肿瘤细胞释放多种趋化因子、细胞因子和生长因子,随后导致肿瘤相关巨噬细胞的募集,而肿瘤相关巨噬细胞反过来又释放大量因子来构建免疫抑制和肿瘤支持性微环境。在本文中,我们综述了胶质母细胞瘤相关巨噬细胞和小胶质细胞的生物学特性,强调了参与肿瘤相关巨噬细胞与胶质母细胞瘤细胞相互作用的新出现的分子靶点和相关信号通路,以及胶质母细胞瘤潜在的与肿瘤相关巨噬细胞相关的治疗靶点。