Scholtes Mathijs P, de Jong Florus C, Zuiverloon Tahlita C M, Theodorescu Dan
Department of Urology, Erasmus MC Cancer Institute, Erasmus University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.
Cedars-Sinai Samuel Oschin Comprehensive Cancer Institute, Los Angeles, CA 90048, USA.
Cancers (Basel). 2021 Jan 14;13(2):288. doi: 10.3390/cancers13020288.
Metabolic reprogramming (MR) is an upregulation of biosynthetic and bioenergetic pathways to satisfy increased energy and metabolic building block demands of tumors. This includes glycolytic activity, which deprives the tumor microenvironment (TME) of nutrients while increasing extracellular lactic acid. This inhibits cytotoxic immune activity either via direct metabolic competition between cancer cells and cytotoxic host cells or by the production of immune-suppressive metabolites such as lactate or kynurenine. Since immunotherapy is a major treatment option in patients with metastatic urothelial carcinoma (UC), MR may have profound implications for the success of such therapy. Here, we review how MR impacts host immune response to UC and the impact on immunotherapy response (including checkpoint inhibitors, adaptive T cell therapy, T cell activation, antigen presentation, and changes in the tumor microenvironment). Articles were identified by literature searches on the keywords or references to "UC" and "MR". We found several promising therapeutic approaches emerging from preclinical models that can circumvent suppressive MR effects on the immune system. A select summary of active clinical trials is provided with examples of possible options to enhance the effectiveness of immunotherapy. In conclusion, the literature suggests manipulating the MR is feasible and may improve immunotherapy effectiveness in UC.
代谢重编程(MR)是生物合成和生物能量途径的上调,以满足肿瘤增加的能量和代谢构建块需求。这包括糖酵解活性,它在增加细胞外乳酸的同时剥夺了肿瘤微环境(TME)的营养物质。这通过癌细胞与细胞毒性宿主细胞之间的直接代谢竞争或通过产生免疫抑制代谢物(如乳酸或犬尿氨酸)来抑制细胞毒性免疫活性。由于免疫疗法是转移性尿路上皮癌(UC)患者的主要治疗选择,MR可能对此类治疗的成功产生深远影响。在这里,我们综述了MR如何影响宿主对UC的免疫反应以及对免疫治疗反应的影响(包括检查点抑制剂、适应性T细胞疗法、T细胞活化、抗原呈递以及肿瘤微环境的变化)。通过对关键词或“UC”和“MR”参考文献的文献检索来识别文章。我们发现临床前模型中出现了几种有前景的治疗方法,可以规避MR对免疫系统的抑制作用。提供了活跃临床试验的精选总结以及增强免疫治疗有效性的可能选择示例。总之,文献表明操纵MR是可行的,并且可能提高UC中免疫治疗的有效性。