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CXCL9 与抗肿瘤免疫相关,并可预测子宫体子宫内膜癌的良好预后

英文原题:CXCL9 correlates with antitumor immunity and is predictive of a favorable prognosis in uterine corpus endometrial carcinoma.

查看英文原题

CXCL9 correlates with antitumor immunity and is predictive of a favorable prognosis in uterine corpus endometrial carcinoma.

PubMed 2023/02/08(内容时间) Front Oncol Q2 · IF 3.4(JCR 2025)

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研究概要

CXCL9 过表达与抗肿瘤免疫相关,并可预测 UCEC 的良好预后。这提示 CXCL9 可能作为 UCEC 患者的独立预后生物标志物或治疗靶点,从而增强抗肿瘤免疫效应以提供生存获益。

研究思路结论见上方概要

C-X-C基序趋化因子配体-9(CXCL9)与多种肿瘤的进展相关。然而,其在子宫体子宫内膜样癌(UCEC)中的生物学功能仍不清楚。在此,我们评估了CXCL9在UCEC中的预后意义和潜在机制。

首先,利用公共癌症数据库的生物信息学分析,包括癌症基因组图谱/基因型-组织表达项目(TCGA+GTEx,n=552)和基因表达综合数据库(GEO):GSE63678(n=7),用于UCEC中CXCL9表达相关分析。然后,对TCGA-UCEC进行生存分析。进一步,进行基因集富集分析(GSEA),以揭示UCEC中与CXCL9表达相关的潜在分子信号通路。此外,使用来自人类标本的验证队列(n=124)的免疫组织化学(IHC)测定来证明CXCL9在UCEC中的潜在意义。

生物信息学分析表明,CXCL9 在 UCEC 患者中表达显著上调;CXCL9 高表达与生存期延长相关。GSEA 富集分析显示,CXCL9 介导了多种免疫应答相关通路,包括 T/NK 细胞、淋巴细胞活化、细胞因子-细胞因子受体相互作用网络以及趋化因子信号通路。此外,细胞毒性分子(IFNG、SLAMF7、JCHAIN、NKG7、GBP5、LYZ、GZMA、GZMB 和 TNF3F9)以及免疫抑制基因(包括 PD-L1)与 CXCL9 的表达呈正相关。进一步,IHC 实验表明 CXCL9 蛋白表达主要定位于肿瘤间质,并在 UCEC 患者中显著上调;肿瘤间质 CXCL9 细胞丰度高的 UCEC 预后更好;在 CXCL9 高表达的 UCEC 中,发现抗肿瘤免疫细胞(CD4 +、CD8 + 和 CD56 + 细胞)比例更高,PD-L1 表达也更高。

展开英文摘要原文

The C-X-C motif chemokine ligand-9 (CXCL9) is related to the progression of multiple neoplasms. Yet, its biological functions in uterine corpus endometrioid carcinoma (UCEC) remain shrouded in confusion. Here, we assessed the prognostic significance and potential mechanism of CXCL9 in UCEC.

Firstly, bioinformatics analysis of the public cancer database, including the Cancer Genome Atlas / the Genotype-Tissue Expression project (TCGA+ GTEx, n=552) and Gene Expression Omnibus (GEO): GSE63678 (n=7), were utilized for the CXCL9 expression-related analysis in UCEC. Then, the survival analysis of TCGA-UCEC was performed. Futher, the gene set enrichment analysis (GSEA) was carried out to reveal the potential molecular signaling pathway in UCEC associated with CXCL9 expression. Moreover, the immunohistochemistry (IHC) assay of our validation cohort (n=124) from human specimens were used to demonstrate the latent significance of CXCL9 in UCEC.

The bioinformatics analysis suggested that CXCL9 expression was significantly upregulated in UCEC patients; and hyper-expression of CXCL9 was related to prolonged survival. the GSEA enrichment analysis showed various immune response-related pathways, including T/NK cell, lymphocyte activation, cytokine-cytokine receptor interaction network, and chemokine signaling pathway, mediated by CXCL9. In addition, the cytotoxic molecules (IFNG, SLAMF7, JCHAIN, NKG7, GBP5, LYZ, GZMA, GZMB, and TNF3F9) and the immunosuppressive genes (including PD-L1) were positively related to the expression of CXCL9. Further, the IHC assay indicated that the CXCL9 protein expression was mainly located in intertumoral and significantly upregulated in the UCEC patients; UCEC with high intertumoral CXCL9 cell abundance harbored an improved prognosis; a higher ratio of anti-tumor immune cells (CD4 + , CD8 + , and CD56 + cell) and PD-L1 was found in UCEC with CXCL9 high expression.

Overexpressed CXCL9 correlates with antitumor immunity and is predictive of a favorable prognosis in UCEC. It hinted that CXCL9 may serve as an independent prognostic biomarker or therapeutic target in UCEC patients, which augmented anti-tumor immune effects to furnish survival benefits.

论文信息

作者
Xue S、Su XM、Ke LN、Huang YG
第一作者单位
Department of obstetrics and gynecology, Sinopharm Dongfeng General Hospital, Hubei University of Medicine, Shiyan, China.China
通讯作者单位
Department of Pathology, Taihe Hospital, Hubei University of Medicine, Shiyan, China.China
期刊
Frontiers in oncology2023
原文标识
PubMed 36845675 · DOI 10.3389/fonc.2023.1077780