WGCNA reveals a biomarker for cancer-associated fibroblasts to predict prognosis in cervical cancer.

Zao-Ling Liu, Nan Chen, Rong Li, Ying-Jie Ma, Aerna Qiayimaerdan, Cai-Ling Ma
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Abstract

Background: Cancer-associated fibroblasts (CAFs) are crucial components of the cervical cancer tumor microenvironment, playing a significant role in cervical cancer progression, treatment resistance, and immune evasion, but whether the expression of CAF-related genes can predict clinical outcomes in cervical cancer is still unknown. In this study, we sought to analyze genes associated with CAFs through weighted gene co-expression network analysis (WGCNA) and to create a predictive model for CAFs in cervical cancer.

Methods: We acquired transcriptome sequencing data and clinical information on cervical cancer patients from the cancer genome atlas (TCGA) and gene expression omnibus (GEO) databases. WGCNA was conducted to identify genes related to CAFs. We developed a prognostic model based on CAF genes in cervical cancer using the least absolute shrinkage and selection operator (LASSO) Cox regression analysis. Single-cell sequencing data analysis and in vivo experiments for validation of hub genes in CAFs.

Results: A prognostic model for cervical cancer was developed based on CAF genes including COL4A1 , LAMC1 , RAMP3 , POSTN , and SERPINF1 . Cervical cancer patients were divided into low- and high-risk groups based on the optimal cutoff value. Patients in the high-risk group had a significantly worse prognosis. Single-cell RNA sequencing data revealed that hub genes in the CAFs risk model were expressed mainly in fibroblasts. The real-time fluorescence quantitative polymerase chain reaction (PCR) results revealed a significant difference in the expression levels of COL4A1 , LAMC1 , POSTN , and SERPINF1 between the cancer group and the normal group ( p < 0.05). Consistently, the results of the immunohistochemical tests exhibited notable variations in COL4A1, LAMC1, RAMP3, POSTN, and SERPINF1 expression between the cancer and normal groups ( p < 0.001).

Conclusion: The CAF risk model for cervical cancer constructed in this study can be used to predict prognosis, while the CAF hub genes can be utilized as crucial markers for cervical cancer prognosis.

WGCNA 揭示了预测宫颈癌预后的癌症相关成纤维细胞生物标志物。
背景:癌症相关成纤维细胞(CAFs)是宫颈癌肿瘤微环境的重要组成部分,在宫颈癌的进展、治疗耐药和免疫逃避中发挥着重要作用,但CAF相关基因的表达能否预测宫颈癌的临床结局仍是未知数。在本研究中,我们试图通过加权基因共表达网络分析(WGCNA)分析与CAFs相关的基因,并建立宫颈癌CAFs的预测模型:我们从 TCGA 和 GEO 数据库中获取了宫颈癌患者的转录组测序数据和临床信息。方法:我们从 TCGA 和 GEO 数据库中获取了宫颈癌患者的转录组测序数据和临床信息,并进行了加权基因共表达网络分析,以确定与 CAFs 相关的基因。我们利用 LASSO Cox 回归分析建立了基于宫颈癌 CAF 基因的预后模型。单细胞测序数据分析和体内实验验证了CAFs中的枢纽基因:结果:基于CAF基因(包括COL4A1、LAMC1、RAMP3、POSTN和SERPINF1)建立了宫颈癌预后模型。根据最佳临界值将宫颈癌患者分为低风险组和高风险组。高风险组患者的预后明显较差。单细胞 RNA 测序数据显示,CAFs 风险模型中的枢纽基因主要在成纤维细胞中表达。实时荧光定量 PCR 结果显示,癌症组与正常组之间 COL4A1、LAMC1、POSTN 和 SERPINF1 的表达水平存在显著差异(P < 0.05)。同样,免疫组化检测结果显示,癌症组与正常组之间 COL4A1、LAMC1、RAMP3、POSTN 和 SERPINF1 的表达也存在显著差异(P < 0.001):结论:本研究构建的宫颈癌CAF风险模型可用于预测预后,而CAF枢纽基因可作为宫颈癌预后的关键标志物。
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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