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钙依赖性黏附蛋白 CDH18,子宫体子宫内膜癌预后的潜在生物标志物

英文原题:Calcium-dependent adhesion protein CDH18, a potential biomarker for prognosis in uterine corpus endometrial carcinoma.

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Calcium-dependent adhesion protein CDH18, a potential biomarker for prognosis in uterine corpus endometrial carcinoma.

PubMed 2025/02/13(内容时间) Front Mol Biosci Q2 · IF 4.4(JCR 2025)

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研究概要

CDH18 是 UCEC 中一种新的有前景的生物标志物,独特地将肿瘤进展、免疫调节和化疗耐药性相关联,提供增强的预后准确性并指导个体化治疗策略以改善患者结局。

研究思路结论见上方概要

子宫体子宫内膜癌(UCEC)是女性最常见的癌症之一,但缺乏特异且敏感的肿瘤标志物用于诊断,因为CA125等传统标志物特异性有限。本研究探讨CDH18(一种与肿瘤进展相关的钙依赖性黏附蛋白)在UCEC中的临床意义和预后价值。

UCEC患者的临床数据来源于癌症基因组图谱(TCGA)数据库。通过泛癌分析、差异表达检测和生存分析,探讨钙相关蛋白CDH18的差异表达及其预后相关性。利用cBioPortal数据库检测UCEC中CDH18的突变情况。其他分析包括功能富集、肿瘤突变负荷、通过ESTIMATE进行肿瘤微环境(TME)评估以及免疫浸润评估,以阐明CDH18在UCEC中的潜在机制。利用药物敏感性测试为患者确定更合适的治疗选择。免疫荧光染色(IF)和实时聚合酶链反应技术(RT-PCR)证实了CDH18在UCEC肿瘤中的表达。

CDH18在UCEC中表达显著升高,并与较差预后显著相关,这一结果经我们的IF和RT-PCR结果证实。共鉴定出13个突变位点,生存分析显示CDH18表达较高的患者总生存期较短。多因素COX回归分析证实CDH18的表达是总生存期的独立预测因子。此外,我们开发了一个预测性列线图模型,用于准确预测UCEC患者的结局。相关性分析显示,CDH18表达与CD8 T细胞水平呈负相关,与静息NK细胞和巨噬细胞M2水平呈正相关。在CDH18高表达组中,(5Z)-7-Oxozeaenol、AG-014699、CEP-701、Mitomycin C、PD-0325901、PD-0332991、PHA-665752、SL 0101-1和SN-38的IC50值显著升高。

展开英文摘要原文

Uterine corpus endometrial carcinoma (UCEC) is one of the most common cancers in women, yet lacks specific and sensitive tumor markers for diagnosis, as traditional markers like CA125 show limited specificity. This study investigates the clinical significance and prognostic value of CDH18, a calcium-dependent adhesion protein linked to tumor progression, in UCEC.

Clinical data from UCEC patients were sourced from The Cancer Genome Atlas (TCGA) database. Pan-cancer analysis, differential expression examination, and survival analysis were conducted to investigate the differential expression of the calcium associated protein-CDH18 and its prognostic relevance. CDH18 mutations in UCEC were examined using the cBioPortal database. Additional analyses included functional enrichment, tumor mutational burden, tumor microenvironment (TME) estimates via ESTIMATE, and immune infiltration assessment to clarify CDH18's potential mechanisms in UCEC. Drug sensitivity testing was utilized to identify more suitable therapeutic options for patients. Immunofluorescence staining (IF) and Real-Time Polymerase Chain Reaction techniques (RT-PCR) confirmed CDH18 expression in UCEC tumor.

CDH18 expression was markedly increased in UCEC and showed a significant association with poorer prognosis, which was confirmed by our IF and RT-PCR results. Thirteen mutation sites were identified, and survival analysis showed that patients with higher CDH18 expression had shorter overall survival. The expression of CDH18 was confirmed to be an independent predictor of overall survival by multivariate COX regression analysis. Additionally, a predictive nomogram model was developed to accurately forecast outcomes for individuals with UCEC. Correlation analysis revealed that CDH18 expression exhibited a negative correlation with CD8 T cell levels and a positive correlation with resting NK cell and macrophage M2 levels. In the group with high CDH18 expression, the IC50 values for (5Z)-7-Oxozeaenol, AG-014699, CEP-701, Mitomycin C, PD-0325901, PD-0332991, PHA-665752, SL 0101-1, and SN-38 were notably elevated.

CDH18 is a novel promising biomarker in UCEC, uniquely associating tumor progression, immune modulation, and chemotherapy resistance, offering enhanced prognostic accuracy and guiding individualized therapeutic strategies for improved patient outcomes.

论文信息

作者
Tang X、Dang S、Qiu J、Zhou R、Ling J、Zhang L、Peng X、Li Q
单位
The Fourth Clinical Medical College of Guangzhou University of Chinese Medicine, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen, Guangdong, China.China
期刊
Frontiers in molecular biosciences2025
原文标识
PubMed 40017628 · DOI 10.3389/fmolb.2025.1530253