含溴结构域蛋白2在抗肿瘤免疫调控中的作用及机制研究OACSTPCD
Regulation mechanism of bromodomain-containing protein 2 for antitumor immunity
目的 研究含溴结构域蛋白2(BRD2)在抗肿瘤免疫调控中的作用及机制,探索新的免疫治疗靶点.方法 利用REMBRANDT胶质瘤数据库分析、GlioVis和TIMER网站在线分析,比较BRD2在肿瘤组织与正常组织中表达水平的差异、BRD2的表达水平与多形性胶质母细胞瘤(GBM)患者预后的相关性,并比较其与GBM肿瘤中免疫细胞浸润的相关性.构建靶向BRD2基因的干涉质粒,包装慢病毒并感染小鼠胶质瘤细胞GL261,灭瘟素筛选感染阳性细胞6 d,Western印迹法检测BRD2蛋白表达水平.CellTiter-Glo试剂盒检测敲低BRD2后GL261的细胞活力.将敲低BRD2的GL261细胞移植入C57BL/6J小鼠皮下形成皮下肿瘤,定期测量肿瘤的体积,并在肿瘤接种后第28天将其取出并分离肿瘤细胞,利用流式细胞术和免疫组化的方法分析皮下瘤组织内CD8+T细胞的浸润情况.结果 BRD2在多种肿瘤组织中高表达,高表达BRD2的胶质瘤患者的预后较差,且BRD2表达水平与肿瘤中CD8+T细胞浸润呈负相关.敲低BRD2后的GL261细胞形成的小鼠皮下移植瘤生长速度减慢,且皮下瘤组织内CD8+T细胞的浸润水平增加.结论 BRD2高表达抑制GBM肿瘤组织内CD8+T细胞的浸润并促进肿瘤的生长.
Objective To investigate the effect and mechanism of bromodomain-containing protein 2(BRD2)on regulation of antitumor immunity,and to explore a novel target for immunotherapy.Methods The REMBRANDT glioma database and GlioVis and TIMER websites were used to compare the expression levels of BRD2 in tumor tissues and normal ones.The correlations between BRD2 expression levels and the prognosis of patients with glioblastoma multiforme(GBM)and those between BRD2 expression levels and immune cell infiltration in GBM were studied.The interference plasmid targeting the BRD2 gene was constructed.The lentivirus was packaged and used to infect murine glioma cells GL261.The positive cells were screened with blasticidin for 6 days,and the expression level of BRD2 protein was detected by Western blot.The CellTiter-Glo kit was used to detect the cell viability of GL261 cells after BRD2 knockdown,which were transplanted into the subcutaneous tissue of C57BL/6J mice to form subcutaneous tumors.The tumor volume was measured periodically.Twenty-eight days after tumor inoculation,the tumors were removed and tumor cells isolated.The infiltration of CD8+T cells within the subcutaneous tumor tissue was analyzed using flow cytometry and immunohistochemistry.Results BRD2 was highly expressed in a variety of tumor tissues.The prognosis of glioma patients with high BRD2 expressions was poor,and the BRD2 expression level was negatively correlated with CD8+T cell infiltration in the tumor.The growth rate of subcutaneously transplanted GL261 tumor cells after BRD2 knockdown was decelerated,and the infiltration level of CD8+T cells in subcutaneous tumor tissue was increased.Conclusion BRD2 over-expression inhibits the infiltration of CD8+T cells in GBM tumors and promotes the growth of tumors.
张诚;李圆圆;李爱玲;满江红
国家生物医学分析中心,北京 100850
临床医学
含溴结构域蛋白2(BRD2)抗肿瘤免疫调控多形性胶质母细胞瘤(GBM)细胞浸润
bromodomain-containing protein 2(BRD2)regulation of antitumor immunityglioblastoma multiforme(GBM)cell infiltration
《军事医学》 2024 (005)
355-361 / 7
国家自然科学基金项目(32270826);国家重点研发计划项目(2022YFA1303000)
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