Qiu Xiaoting, Liu Peizhang, Lin Hongxiang, Peng Zeyi, Sun Xinhao, Dong Guanting, Han Yuanyuan, Huang Zhijian
Department of Breast Surgical Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, 350014, China.
School of Basic Medical Sciences, Fujian Medical University, Fuzhou, 350108, China.
Discov Oncol. 2025 Mar 17;16(1):330. doi: 10.1007/s12672-025-02094-1.
This study investigates Cytochrome B561 (CYB561) expression in Pan-Cancer, its relationship with immune invasion, and its prognostic value in Breast Cancer (BRCA) patients.
Data from The Cancer Genome Atlas (TCGA) were analyzed. CYB561 expression in normal and tumor tissues was examined, with correlations to immune invasion, mutation, and immune checkpoints. Wilcoxon rank-sum test assessed expression differences. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were conducted. Logistic regression, Kaplan-Meier, and Cox regression analyses evaluated clinicopathological features and survival outcomes. A Cox multivariate analysis-based Nomogram predicted CYB561's prognostic impact. CYB561 knockout in breast cancer cells assessed functional effects. Single-cell RNA sequencing identified prognostic biomarkers.
CYB561 was highly expressed in most tumors. BRCA showed the highest correlation with ESTIMATE scores and significant negative correlation with immune checkpoints. High CYB561 expression correlated with specific clinicopathological features and survival outcomes. The nomogram predicted BRCA prognosis. CYB561 knockout inhibited breast cancer cell proliferation. Seven predictive agents for CYB561 inhibition were identified.
CYB561 exhibits aberrant expression in tumors, particularly in BRCA, and serves as a predictive marker for immune-related therapies and a prognostic indicator in BRCA.
本研究调查细胞色素B561(CYB561)在泛癌中的表达、其与免疫浸润的关系以及其在乳腺癌(BRCA)患者中的预后价值。
分析来自癌症基因组图谱(TCGA)的数据。检测正常组织和肿瘤组织中CYB561的表达,并分析其与免疫浸润、突变及免疫检查点的相关性。采用Wilcoxon秩和检验评估表达差异。进行基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析。通过逻辑回归、Kaplan-Meier分析和Cox回归分析评估临床病理特征和生存结果。基于Cox多变量分析的列线图预测CYB561的预后影响。对乳腺癌细胞进行CYB561基因敲除以评估其功能效应。单细胞RNA测序鉴定预后生物标志物。
CYB561在大多数肿瘤中高表达。BRCA与ESTIMATE评分的相关性最高,与免疫检查点呈显著负相关。CYB561高表达与特定临床病理特征和生存结果相关。列线图可预测BRCA的预后。CYB561基因敲除抑制乳腺癌细胞增殖。鉴定出7种CYB561抑制的预测因子。
CYB561在肿瘤中呈现异常表达,尤其是在BRCA中,可作为免疫相关治疗的预测标志物和BRCA的预后指标。