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程序性死亡受体1/程序性死亡受体1配体在食管癌中的研究进展 被引量:1

Progress of programmed death-1/programmed death-1 ligand in esophageal cancer
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摘要 程序性死亡受体1(PD-1)在人类多种免疫细胞和肿瘤细胞中广泛存在,当与程序性死亡受体1配体(PD-L1)结合后可耗竭T细胞致肿瘤免疫逃逸.体内外实验证实抑制PD-1与其配体结合,阻断下游信号通路可增强机体内源性抗肿瘤免疫效应.PD-1/PD-L1的表达不仅与食管癌患者临床分期及预后相关,还有可能成为临床生物标志物,而成为肿瘤免疫治疗的新靶点.文章就PD-1/PD-L1与食管癌的关系及相关治疗方案的最新研究进行综述. Programmed death-1 (PD-1) occurs widely in a variety of human immune cells and tumor cells. When PD-1 is combined with programmed death-1 ligand (PD-L1), T-lymphocyte will be exhausted eventually resulting in tumor immune escape. Experiments in vitro and in vivo have demonstrated that inhibiting the binding of PD-1 with PD-L1, and blocking downstream signaling pathways can enhance endogenous anti-neoplastic immune effects. The expression of PD-1/PD-L1 is related to the clinical stage and prognosis of esophageal cancer patients, which may become the clinical biomarkers, serving as a new target for cancer immunotherapy.This paper reviews the relationship between PD-1/PD-L1 and esophageal cancer as well as the related treatment progress.
出处 《肿瘤研究与临床》 CAS 2017年第11期776-780,共5页 Cancer Research and Clinic
基金 四川省卫生和计划生育委员会科研课题(17ZD006)
关键词 食管肿瘤 程序性死亡受体1 程序性死亡受体1配体 肿瘤免疫 Programmed death-1 Esophageal neoplasms Programmed death-1 ligand Tumor immunity
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