Department of Oncology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Laboratory of Molecular Pharmacology, Southwest Medical University, Luzhou, 646000, Sichuan, PR China.
Theranostics. 2020 May 15;10(14):6231-6244. doi: 10.7150/thno.45219. eCollection 2020.
During the last few decades, cell-based anti-tumor immunotherapy emerged and it has provided us with a large amount of knowledge. Upon chemokines recognition, immune cells undergo rapid trafficking and activation in disease milieu, with immune cells chemotaxis being accompanied by activation of diverse intercellular signal transduction pathways. The outcome of chemokines-mediated immune cells chemotaxis interacts with the cue of mammalian target of rapamycin (mTOR) in the tumor microenvironment (TME). Indeed, the mTOR cascade in immune cells involves migration and infiltration. In this review, we summarize the available mTOR-related chemokines, as well as the characterized upstream regulators and downstream targets in immune cells chemotaxis and assign potential underlying mechanisms in each evaluated chemokine. Specifically, we focus on the involvement of mTOR in chemokine-mediated immune related cells in the balance between tumor immunity and malignancy.
在过去的几十年中,基于细胞的抗肿瘤免疫疗法已经出现,它为我们提供了大量的知识。在趋化因子识别后,免疫细胞在疾病环境中迅速迁移和激活,免疫细胞的趋化作用伴随着各种细胞间信号转导途径的激活。趋化因子介导的免疫细胞趋化的结果与肿瘤微环境(TME)中哺乳动物雷帕霉素靶蛋白(mTOR)的线索相互作用。事实上,mTOR 级联在免疫细胞中涉及迁移和浸润。在这篇综述中,我们总结了现有的与 mTOR 相关的趋化因子,以及免疫细胞趋化作用中特征化的上游调节剂和下游靶点,并在每个评估的趋化因子中分配了潜在的潜在机制。具体来说,我们专注于 mTOR 在趋化因子介导的免疫相关细胞中在肿瘤免疫和恶性之间的平衡中的作用。