期刊文献+

PD-1/PD-L1在治疗三阴性乳腺癌中的研究进展 被引量:6

Research Progress of PD-1/PD-L1 in Triple-Negative Breast Cancer Treatment
原文传递
导出
摘要 越来越多的研究表明机体的免疫系统在乳腺癌的治疗和预后中起重要作用,其中免疫检查点阻滞剂是免疫疗法中快速发展的领域。迄今为止乳腺癌的研究中备受关注的是三阴性乳腺癌(TNBC)的治疗,这是一种基因组不稳定的乳腺癌亚型,被认为是最具有免疫原性的乳腺癌,其患者只有有限的治疗选择,并且预后较差。程序性死亡配体1(PD-L1)在三阴性乳腺癌中的表达水平高于其他亚型,协助肿瘤实现免疫逃逸,所以相应的阻滞剂更能在该亚型中发挥抗肿瘤的作用。文章从单一疗法和组合疗法两个方面阐述了程序性死亡因子1(PD-1)及其配体的免疫检查点阻滞剂在三阴性乳腺癌中的研究进展。 Accumulating evidence confirms that the host immune system plays an important role in treatment and prognosis of breast cancer.Immunotherapy with immune checkpoint inhibitors is a promising and rapidly growing field.The study largely focused on the treatment of triple-negative breast cancer(TNBC),a genomically unstable subtype of breast cancer that is believed to be the most immunogenic with limited treatment options and a particularly poor prognosis.Compared with other intrinsic breast cancer subtypes,TNBC has higher programmed death-ligand 1(PD-L1)expression levels,which may help tumor immune evasion by suppressing immune responses.Thus,checkpoint inhibitor can enhance antitumor T-cell responses in TNBC.In this review,the author discusses the current study for PD-1/PD-L1 blockade in metastatic triple-negative breast cancer(TNBC)treatment.Both checkpoint inhibitor monotherapy and combinations with chemotherapy are being investigated.The author also proposes potential ways of improving responses to checkpoint blockade in breast cancer.
作者 林炳静 徐寒梅 孙晴波 胡加亮 LIN Bing-jing;XU Han-mei;SUN Qing-bo;HU Jia-liang(Engineering Research Center of Synthetic Polypeptide Drug Discovery and Evaluation of Jiangsu Province,China Pharmaceutical University,Nanjing 211198,China)
出处 《药物生物技术》 CAS 2019年第1期69-72,共4页 Pharmaceutical Biotechnology
关键词 三阴性乳腺癌 免疫检查点阻滞剂 免疫治疗 程序性死亡因子1 肿瘤浸润性淋巴细胞 组合疗法 Triple-negative breast cancer Immune checkpoint blockers Immunotherapy Programmed cell death-1 Tumor infiltrating lymphocytes Combination therapy
  • 相关文献

参考文献1

二级参考文献38

  • 1M E Van Meter, E S Kim. Bevacizumab:current updates in treat- ment[J]. Curr Opin Oncol,2010,22:586-591.
  • 2P Boross, S Lohse, M Nederend ,et al. IgA EGFR antibodies medi-ate tumour killing in vivo [ J ]. EMBO Mol Med, 2013, 5 : 1213-1226.
  • 3H Modjtahedi, S Ali, S Essapen. Therapeutic application of mono- clonal antibodies in cancer: advances and ehallenges[-J]. Br Med Bull,2012,104:41-59.
  • 4Curigliano G, Spitaleri G, Pietri E,et al. Breast cancer vaccines : a clinical reality or fairy tale. [ J ]. Ann Oncol, 2006, 17 ( 5 ) : 750-762.
  • 5Cleator S, Heller W, Coombes RC. Triple-negative breast cancer: therapeutic options [ J ]. Lancet Oncol, 2007,8 : 235-244.
  • 6Arteaga CL, Sliwkowski MX, Osborne CK, et al. Treatment of HER2-positive breast cancer: current status and future perspec- tives [ J ] . Nat Rev Clin Oncol ,2011,9 :16-32.
  • 7Zhou B, Hung M. Dysregulation of cellular signaling by HER-2/ neu in breast cancer[J]. Semin Oncol,2003,30(16) :38-48.
  • 8Larbouret C, Gaborit N, Chardes T, et al. In pancreatic carcino- ma, dual EGFR/HER2 targeting with cetuximab/trastuzumab is more effective than treatment with trastuzumab/erlotinib or lapa- tinib alone : implication of receptors' down-regulation and dimers' disruption [ J]. Neoplasia ,2012,14 : 121-130.
  • 9Zhou H,Zha Z,Liu Y,et al. Structural insights into the down-reg- ulation of overexpressed p185 (her2/neu) protein of transformed cells by the antibody chA21 [ J]. Biol Chem, 2011,28 (3): 1676-1683.
  • 10Disis ML, Shiota FM, Cheever MA. Human HER-2/neu protein immunization circumvents tolerance to rat neu : a vaccine strategy for-self, tumourantigens [ J ]. Immunology, 1998, 93 ( 2 ) : 192-199.

共引文献5

同被引文献99

引证文献6

二级引证文献20

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