探讨子宫内膜癌中 GRHL1 表达与肿瘤微环境及免疫疗法之间的相关性

Suyang Guo, Wenqi Bai, Fengjie Cui, Xin Chen, Xiaojing Fang, Honghong Shen, Xianhua Gu
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摘要

简介GRHL1属于类谷粒头(GRHL)家族。以往的研究表明,生长和生存途径的失调与 GRHL 家族基因癌症有关。检查点抑制剂的免疫疗法改变了包括子宫内膜癌(EC)在内的许多肿瘤的治疗模式。然而,人们对GRHL1对子宫内膜癌免疫疗法的影响及其与免疫细胞浸润的关系知之甚少:方法:通过搜索 TCGA 数据库分析了 EC 组织和正常 EC 组织中 GRHL1 的差异表达,并利用免疫组化分析验证了结果。接下来,研究人员还调查了GRHL1、CD8+ T细胞和肿瘤微环境(TME)之间的关系,并评估了GRHL1的表达对EC免疫治疗的影响:结果:研究发现,相对于正常组织,EC组织的GRHL1表达水平较高。高水平表达GRHL1的EC患者的总生存期(OS)和无进展生存期(PFS)均低于低水平表达者。此外,GRHL1的表达与CD8+ T细胞呈负相关,GRHL1高表达的患者接受免疫治疗的效果较差:结论:GRHL1在EC患者中高表达,高表达的GRHL1会抑制EC肿瘤微环境中CD8+ T细胞的增殖,影响免疫治疗的疗效:GRHL1、子宫内膜癌、肿瘤微环境、CD8+T细胞、免疫治疗
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Exploration of the Correlation Between GRHL1 Expression and Tumor Microenvironment in Endometrial Cancer and Immunotherapy
Introduction: GRHL1 belongs to the family of Grainyhead-like (GRHL). Previous studies have shown that dysregulation of growth and survival pathways is associated with the GRHL family of gene cancers. Immunotherapy with checkpoint inhibitors has changed the treatment paradigm for many tumors, including endometrial cancer (EC). However, the effect of GRHL1 on immunotherapy in EC and its relationship with immune cell infiltration are poorly understood.
Methods: Differential expression of GRHL1 between EC and normal EC tissues was analyzed by searching the TCGA database, and the results were verified utilizing immunohistochemistry analyses. Next, the relationship between GRHL1, CD8+ T cells and tumor microenvironment (TME) was also investigated, and the effect of GRHL1 expression on immunotherapy in EC was evaluated.
Results: According to the findings, EC tissues had elevated expression levels of GRHL1 relative to normal tissues. Patients with EC who expressed GRHL1 at high levels experienced worse overall survival (OS) and Progression-free survival (PFS) than those whose expression was lower. In addition, GRHL1 expression was negatively correlated with CD8+ T cells, and patients with high GRHL1 expression were less effective in receiving immunotherapy.
Conclusion: The expression of GRHL1 was high in EC patients, and high expression of GRHL1 inhibits the proliferation of CD8+ T cells in the tumor microenvironment of EC and affect the efficacy of immunotherapy.

Keywords: GRHL1, endometrial cancer, tumor microenvironment, CD8+ T cells, immunotherapy
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