成人H3K27-变异型弥漫性中线胶质瘤蛋白质组特征分析OA
Proteomic characteristic analysis of adult H3K27-altered diffuse midline glioma
目的 分析成人 H3K27-变异型弥漫性中线胶质瘤(DMG)的临床病理学资料,结合肿瘤组织的蛋白质差异表达信息,探讨成人 H3K27-变异型 DMG 的特征,为疾病提供更加全面的诊断线索.方法 收集 8 例 H3K27-变异型DMG 成人患者的临床病理资料,使用激光显微切割结合质谱技术对肿瘤组织标本进行蛋白质组学分析.将筛选出的差异表达蛋白质进行功能分析,并选择其中重要的差异表达蛋白质进行免疫组织化学验证.结果 此次组织样本共鉴定到 6 171 个蛋白质.与对照组相比,在肿瘤组中鉴定到 867 个差异表达蛋白质;与瘤旁组相比,肿瘤组中鉴定到 277 个差异蛋白质.主要与 mRNA 和蛋白质合成有关.其中在肿瘤组织中高表达的 CTBP2、YBX1、SRSF1 和 SRSF2 得到了免疫组化的验证(P<0.05).结论 成人 H3K27-变异型 DMG 的肿瘤组织具有显著的蛋白质组特征差异,可以为诊断提供更全面的信息.
Objective To investigate pathological characteristics of adult H3K27-altered diffuse midline glioma(DMG)and differential protein expression in tumor brain tissue,for providing more comprehensive diagnostic clues.Methods Clinical and pathological data from eight adult patients with H3K27-altered DMG were collected.Proteomics analysis of tumor tissue was performed using laser microdissection combined with mass spectrometry.Differentially expressed proteins were screened for functional analysis,and four key proteins among these proteins were selected for immuno-histochemical validation.Results A total of 6 171 proteins were identified in these tissue samples.Compared with the non-tumor control group,867 proteins were significantly expressed in the tumor group;compared with the para-neoplastic group,277 proteins were significantly expressed tumor group.It was mainly related to mRNA synthesis and protein synthesis.CTBP2,YBX1,SRSF1,and SRSF2,which were significantly up-regulated in tumor tissues,were verified by immuno-histochemistry(P<0.05).Conclusions The tumor tissue exhibits significant proteomic characteristic differences.Differential protein expression analysis can provide more comprehensive information to support diagnosis.
倪艳颖;翟春颜;沈萍;张繁霜;姜忠彩
航空总医院 病理科,北京 100012航空总医院 病理科,北京 100012航空总医院 病理科,北京 100012国家癌症中心/国家肿瘤临床研究中心/中国医学科学院北京协和医学院 肿瘤医院 病理科,北京 100021航空总医院 病理科,北京 100012
医药卫生
H3K27-变异型弥漫性中线胶质瘤成人临床病理特征差异蛋白质
H3K27-altered diffuse midline gliomaadultpathological characteristicdifferential proteins
《基础医学与临床》 2026 (5)
607-613,7
国家自然科学基金(82403823)
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