Liu Liling, Yang Yuanzhong, Duan Hao, He Jiahua, Sun Lu, Hu Wanming, Zeng Jing
Department of Pathology, Sun Yat-Sen University Cancer Center, Guangzhou, China.
State Key Laboratory of Oncology in Southern China, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Front Oncol. 2021 Apr 15;11:611038. doi: 10.3389/fonc.2021.611038. eCollection 2021.
CHI3L2 (Chitinase-3-Like Protein 2) is a member of chitinase-like proteins (CLPs), which belong to the glycoside hydrolase 18 family. Its homologous gene, CHI3L1, has been extensively studied in various tumors and has been shown to be related to immune infiltration in breast cancer and glioblastoma. High CHI3L2 expression was reported to be associated with poor prognosis in breast cancer and renal cell carcinoma. However, the prognostic significance of CHI3L2 in glioma and its correlation between immune infiltration remains unclear. In this study, we examined 288 glioma samples by immunohistochemistry to find that CHI3L2 is expressed in tumor cells and macrophages in glioma tissues and highly expressed in glioblastoma and IDH wild-type gliomas. Relationships between CHI3L2 expression and clinical features (grade, age, Ki67 index, P53, PHH3 (mitotic figures), ATRX, TERTp, MGMTp, IDH, and 1p/19q co-deleted status) were evaluated. Kaplan-Meier survival was conducted to show high CHI3L2 expression in tumor cells (TC) and macrophage cells (MC) indicated poor prognosis in diffusely infiltrating glioma (DIG), lower-grade glioma (LGG), and IDH wild-type gliomas (IDH-wt). The overall survival time was higher in patients with dual-low CHI3L2 expression in TC and MC compared to those in patients with non-dual CHI3L2 expression and dual high expression in DIG and IDH wild-type gliomas. By univariate and multivariate analysis, we found that high CHI3L2 expression in tumor cells was an independent unfavorable prognostic factor in glioma patients. Moreover, we used two datasets (TCGA and CGGA) to verify the results of our study and explore the potential functional role of CHI3L2 by GO and KEGG analyses in gliomas. TIMER platform analysis indicated CHI3L2 expression was closely related to diverse marker genes of tumor immune infiltrating cells, including monocytes, TAMs, M1 macrophages, M2 macrophages, TGFβ1+ Treg and T cell exhaustion in GBM and LGG. Western Blot validated CHI3L2 is expressed in glioma cells and microglia cells. The results of flow cytometry showed that CHI3L2 induces the apoptosis of CD8+ T cells. In conclusion, these results demonstrate CHI3L2 is related to poor prognosis and immune infiltrates in gliomas, suggesting it may serve as a promising prognostic biomarker and represent a new target for glioma patients.
几丁质酶-3-样蛋白2(CHI3L2)是几丁质酶样蛋白(CLPs)家族的成员,该家族属于糖苷水解酶18家族。其同源基因CHI3L1已在多种肿瘤中得到广泛研究,并已证明与乳腺癌和胶质母细胞瘤中的免疫浸润有关。据报道,CHI3L2高表达与乳腺癌和肾细胞癌的不良预后相关。然而,CHI3L2在胶质瘤中的预后意义及其与免疫浸润的相关性仍不清楚。在本研究中,我们通过免疫组织化学检测了288例胶质瘤样本,发现CHI3L2在胶质瘤组织的肿瘤细胞和巨噬细胞中表达,并在胶质母细胞瘤和异柠檬酸脱氢酶(IDH)野生型胶质瘤中高表达。评估了CHI3L2表达与临床特征(分级、年龄、Ki67指数、P53、磷酸化组蛋白H3(有丝分裂象)、α地中海贫血/智力低下综合征X连锁基因(ATRX)、端粒酶逆转录酶启动子(TERTp)、O6-甲基鸟嘌呤-DNA甲基转移酶启动子(MGMTp)、IDH、1号染色体短臂/19号染色体长臂共缺失状态)之间的关系。进行Kaplan-Meier生存分析以显示肿瘤细胞(TC)和巨噬细胞(MC)中CHI3L2高表达表明弥漫性浸润性胶质瘤(DIG)、低级别胶质瘤(LGG)和IDH野生型胶质瘤(IDH-wt)预后不良。与DIG和IDH野生型胶质瘤中CHI3L2非双低表达和双高表达的患者相比,TC和MC中CHI3L2双低表达患者的总生存时间更长。通过单因素和多因素分析,我们发现肿瘤细胞中CHI3L2高表达是胶质瘤患者独立的不良预后因素。此外,我们使用两个数据集(癌症基因组图谱(TCGA)和中国胶质瘤基因组图谱(CGGA))来验证我们的研究结果,并通过基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析探索CHI3L2在胶质瘤中的潜在功能作用。肿瘤免疫估计资源(TIMER)平台分析表明,CHI3L2表达与肿瘤免疫浸润细胞的多种标记基因密切相关,包括胶质母细胞瘤和LGG中的单核细胞、肿瘤相关巨噬细胞(TAM)、M1巨噬细胞、M2巨噬细胞、转化生长因子β1(TGFβ1)+调节性T细胞(Treg)和T细胞耗竭。蛋白质免疫印迹法验证了CHI3L2在胶质瘤细胞和小胶质细胞中表达。流式细胞术结果显示,CHI3L2诱导CD8+T细胞凋亡。总之,这些结果表明CHI3L2与胶质瘤的不良预后和免疫浸润有关,提示它可能是一种有前景的预后生物标志物,并代表胶质瘤患者的一个新靶点。