期刊文献+

Emerging role of metabolic reprogramming in tumor immune evasion and immunotherapy 被引量:6

原文传递
导出
摘要 Mounting evidence has revealed that the therapeutic efficacy of immunotherapies is restricted to a small portion of cancer patients.A deeper understanding of how metabolic reprogramming in the tumor microenvironment(TME)regulates immunity remains a major challenge to tumor eradication.It has been suggested that metabolic reprogramming in the TME may affect metabolism in immune cells and subsequently suppress immune function.Tumor cells compete with infiltrating immune cells for nutrients and metabolites.Notably,the immunosuppressive TME is characterized by catabolic and anabolic processes that are critical for immune cell function,and elevated inhibitory signals may favor cancer immune evasion.The major energy sources that supply different immune cell subtypes also undergo reprogramming.We herein summarize the metabolic remodeling in tumor cells and different immune cell subtypes and the latest advances underlying the use of metabolic checkpoints in antitumor immunotherapies.In this context,targeting both tumor and immune cell metabolic reprogramming may enhance therapeutic efficacy.
出处 《Science China(Life Sciences)》 SCIE CAS CSCD 2021年第4期534-547,共14页 中国科学(生命科学英文版)
基金 supported by the National Natural Science Foundation of China(81903138,81972776,81803025,81772928,81702907,81772901,81672993,81672683) the Natural Science Foundation of Hunan Province(2019JJ50778,2018SK21210,2018SK21211,2018JJ3704,2018JJ3815)。
  • 相关文献

参考文献4

二级参考文献128

  • 1Xin Zhang, Xin-Rong Yang, Xiao-Wu Huang, Wei-Min Wang, Ruo-Yu Shi, Yang Xu, Zheng Wang, Shuang-Jian Qiu, Jia Fan ,Jian Zhou Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai Key Laboratory for Organ Transplantation, Shanghai 200032, China,Institute of Biomedical Sciences, Fudan University, Shanghai 200032, China.Sorafenib in treatment of patients with advanced hepatocellular carcinoma:a systematic review[J].Hepatobiliary & Pancreatic Diseases International,2012,11(5):458-466. 被引量:29
  • 2Janeway CA Jr, Medzhitov R. Innate immune recognition. Annu Rev Immuno12002; 20:197-216. 被引量:1
  • 3Chen GY, Nunez G. Sterile inflammation: sensing and react- ing to damage. Nat Rev lmmuno12010; 10:826-837. 被引量:1
  • 4Warburg O, Wind F, Negelein E. The metabolism of tumors in the body. JGen Physiol 1927; 8:519-530. 被引量:1
  • 5Sbarra AJ, Karnovsky ML. The biochemical basis of phago- cytosis. I. Metabolic changes during the ingestion of parti- cles by polymorphonuclear leukocytes. J Biol Chem 1959; 234:1355-1362. 被引量:1
  • 6Guthrie LA, McPhail LC, Henson PM, Johnston Jr RB. Prim- ing of neutrophils for enhanced release of oxygen metabolites by bacterial lipopolysaccharide. Evidence for increased ac- tivity of the superoxide-producing enzyme. J Exp Med 1984; 160:1656-1671. 被引量:1
  • 7Borregaard N, Herlin T. Energy metabolism of human neutro- phils during phagocytosis. J Clin Invest 1982; 70:550-557. 被引量:1
  • 8Hard GC. Some biochemical aspects of the immune macro- phage. BrJExp Pathol 1970; 51:97-105. 被引量:1
  • 9Newsholme P, Gordon S, Newsholme EA. Rates of utiliza- tion and fates of glucose, glutamine, pyruvate, fatty acids and ketone bodies by mouse macrophages. Biochem J 1987; 242:631-636. 被引量:1
  • 10Newsholme P, Curi R, Gordon S, Newsholme EA. Metabo- lism of glucose, glutamine, long-chain fatty acids and ketone bodies by murine macrophages. Biochem J 1986; 239:121- 125. 被引量:1

共引文献124

同被引文献39

引证文献6

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部