Expression of HECTD2 predicts peritoneal metastasis of gastric cancer and reconstructs immune microenvironment.

IF 5.3 2区 医学 Q1 ONCOLOGY
Libao Gong, Jiayi Huang, Xue Bai, Lin Song, Junjie Hang, Jinfeng Guo
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引用次数: 0

Abstract

Peritoneal metastasis (PM) is a common metastasis site and death cause of gastric cancer, which is a complex biological process, but there is currently a lack of effective prediction and treatment targets. In this study, we first analyzed the differential gene expression of gastric cancer patients with or without peritoneal metastasis, and identified the HECT domain E3 ubiquitin protein ligase 2 (HECTD2) as the core gene of PM in gastric cancer. The current study shows that the role of HECTD2 in tumor is contradictory. In this study, our results show that the low expression of HECTD2 indicates that the survival rate of overall survival (OS), progression-free survival (PFS), disease-specific survival (DSS), and disease-free survival (DFS) are better, and can be used as an important component of prognostic indicators. In addition, through pathway enrichment analysis, we found that HECTD2 was mainly involved in metastasis related pathways such as extracellular matrix remodeling and cell adhesion in gastric cancer, and high expression of HECTD2 could activate epithelial-mesenchymal transition (EMT) metastasis related pathways in gastric cancer. In regulating the metastasis of gastric cancer cells, HECTD2 can also change the surrounding microenvironment, induce the enrichment of interstitial components and build an immune microenvironment conducive to tumor progression, while patients with low expression of HECTD2 may be more likely to benefit from immunotherapy. In conclusion, HECTD2 may be a novel biomarker for the diagnosis and prognosis of peritoneal metastasis of gastric cancer, providing basis for the mechanism of peritoneal metastasis of cancer and clinical medication.

HECTD2的表达可预测胃癌的腹膜转移并重建免疫微环境。
腹膜转移(PM)是胃癌常见的转移部位和死亡原因,是一个复杂的生物学过程,但目前缺乏有效的预测和治疗靶点。在本研究中,我们首先分析了有或无腹膜转移的胃癌患者的差异基因表达,发现HECT结构域E3泛素蛋白连接酶2(HECTD2)是胃癌PM的核心基因。目前的研究表明,HECTD2在肿瘤中的作用是相互矛盾的。在本研究中,我们的结果显示,HECTD2的低表达表明总生存期(OS)、无进展生存期(PFS)、疾病特异性生存期(DSS)和无病生存期(DFS)的生存率较好,可作为预后指标的重要组成部分。此外,通过通路富集分析,我们发现HECTD2主要参与胃癌细胞外基质重塑和细胞粘附等转移相关通路,HECTD2的高表达可激活胃癌上皮-间质转化(EMT)转移相关通路。在调控胃癌细胞转移的同时,HECTD2 还能改变周围微环境,诱导间质成分的富集,构建有利于肿瘤进展的免疫微环境,而低表达 HECTD2 的患者可能更容易从免疫治疗中获益。总之,HECTD2可能是胃癌腹膜转移诊断和预后的新型生物标志物,为癌症腹膜转移机制和临床用药提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.90
自引率
1.70%
发文量
360
审稿时长
1 months
期刊介绍: Cancer Cell International publishes articles on all aspects of cancer cell biology, originating largely from, but not limited to, work using cell culture techniques. The journal focuses on novel cancer studies reporting data from biological experiments performed on cells grown in vitro, in two- or three-dimensional systems, and/or in vivo (animal experiments). These types of experiments have provided crucial data in many fields, from cell proliferation and transformation, to epithelial-mesenchymal interaction, to apoptosis, and host immune response to tumors. Cancer Cell International also considers articles that focus on novel technologies or novel pathways in molecular analysis and on epidemiological studies that may affect patient care, as well as articles reporting translational cancer research studies where in vitro discoveries are bridged to the clinic. As such, the journal is interested in laboratory and animal studies reporting on novel biomarkers of tumor progression and response to therapy and on their applicability to human cancers.
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