International Medicine and Health Guidance News ›› 2023, Vol. 29 ›› Issue (11): 1481-1485.DOI: 10.3760/cma.j.issn.1007-1245.2023.11.001

• New Medical Advances •     Next Articles

Research progress of programmed cell death-1 inhibitors in the treatment of thyroid carcinoma

Wang Yifei, Xue Haibo   

  1. Department of Endocinology, Binzhou Medical University Hospital, Binzhou 256603, China

  • Received:2023-01-30 Online:2023-06-01 Published:2023-06-25
  • Contact: Xue Haibo, Email: xuehaibo@sina.com
  • Supported by:

    Natural Science Foundation of Shandong Province (ZR2022MH175); Innovation Program of Post-graduate Education of Shandong Province (20038612); Scientific Research and Innovation Team Project of Binzhou Medical University Hospital (202031); Reserve Leading Talents Project of Binzhou Medical University Hospital (JC2019-03)

程序性死亡受体1抑制剂治疗甲状腺癌的研究进展

王艺霏  薛海波   

  1. 滨州医学院附属医院内分泌科,滨州 256603

  • 通讯作者: 薛海波,Email:xuehaibo@sina.com
  • 基金资助:

    山东省自然科学基金(ZR2022MH175);山东省研究生教育创新计划项目(20038612);滨州医学院附属医院科研创新团队项目(202031);滨州医学院附属医院后备领军人才项目(JC2019-03)

Abstract:

Programmed cell death-1 (PD-1) / programmed cell death-ligand 1 (PD-L1) are important immune checkpoints, which play pivotal roles in suppressing anti-cancer immunity and are involved in immune escape mechanism of tumor cells. PD-1/PD-L1 inhibitors have achieved remarkable therapeutic effects in non-small-cell lung cancer, advanced melanoma, thyroid carcinoma, and other tumors by blocking the binding of PD-1 on activated T-cells to PD-L1 expressed on tumor cells. This paper mainly reviews the progress in PD-1 inhibitors in the treatment of thyroid carcinoma.

Key words:

Thyroid carcinoma, Immune checkpoint inhibitors, Programmed cell death-1, Molecular targeted therapy, Progress

摘要:

程序性死亡受体1(programmed cell death 1,PD-1)/程序性死亡配体1(programmed cell death-ligand 1,PD-L1)是重要的免疫检查点,在抑制抗肿瘤免疫反应中起作用,参与肿瘤细胞免疫逃逸机制。PD-1/PD-L1抑制剂通过阻断活化的T细胞上的PD-1与表达PD-L1的肿瘤细胞结合,在非小细胞肺癌、晚期黑色素瘤、甲状腺癌等多种肿瘤治疗中取得了良好的治疗效果。本文主要对PD-1抑制剂在甲状腺癌治疗中的研究进展进行综述。

关键词:

甲状腺癌, 免疫检查点抑制剂, 程序性死亡受体1, 分子靶向治疗, 进展