Li Yilun, Ding Baifang, Wei Mengyu, Yang Xiaolu, Fu Ruihuan, Liu Yinfeng, Zhu Lin, Ding Yan, Zhang Wenjin, Zhang Geng, Zhang Shuo, Bu Yuhui, He Jianchao, Deng Jianye, Bao Xiaohuan, Hao Jun, Ma Li
Department of Breast Disease Center, the Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Department of Breast Surgery, Panjin central hospital, Panjin, China.
Asia Pac J Clin Oncol. 2025 Feb;21(1):12-30. doi: 10.1111/ajco.14130. Epub 2024 Oct 12.
Rab11A is an important molecule for recycling endosomes and is closely related to the proliferation, invasion, and metastasis of tumors. This study investigated the prognostic and immune significance of Rab11A and validated its potential function and mechanism in breast cancer (BRCA).
RNA sequencing data for 33 tumors were downloaded from The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression databases. Correlation analysis was used to evaluate the relationship between Rab11A expression and immune characteristics. Potential pathways were identified using the Kyoto Encyclopedia of Genes and Genomes and Gene Ontology analysis. Immunohistochemical analysis, colony formation assay, bromodeoxyuridine incorporation assay, immunofluorescence, and Western blot were used to explore potential function and mechanism.
Analysis of the TCGA database showed significant upregulation of Rab11A expression in a variety of cancers. Rab11A was up-regulated in 82.4% of BRCA. High Rab11A expression is associated with poor survival in cancer patients and is a predictor of poor prognosis. CIBERSORT analysis showed that Rab11A was negatively associated with almost all immune cycle activity scores pan-cancer. The results of the TCGA-BRCA cohort were further confirmed by using pathological samples from clinical BRCA patients. The results showed that Rab11A expression was correlated with estrogen receptor (ER) and progesterone receptor expression in BRCA (p < 0.05). Knockdown and overexpression of Rab11A affected the proliferation of BRCA cells. Further mechanistic studies revealed that down-regulation of ER alpha (ERα) and up-regulation of ER beta (ERβ) mediated Rab11A-induced inhibition of BRCA cell proliferation.
Rab11A expression in pan-cancer is associated with poor prognosis and immune profile. In particular, in BRCA, Rab11A expression regulates cell proliferation by targeting ERα and ERβ. High Rab11A expression is tightly associated with immune characteristics, tumor microenvironment, and genetic mutations. These results provide a reference for exploring the role of Rab11A in pan-cancer and provide a new perspective for revealing potential therapeutic targets in BRCA.
Rab11A是参与回收型内体的重要分子,与肿瘤的增殖、侵袭和转移密切相关。本研究探讨Rab11A的预后及免疫意义,并验证其在乳腺癌(BRCA)中的潜在功能和机制。
从癌症基因组图谱(TCGA)和基因型-组织表达数据库下载33例肿瘤的RNA测序数据。采用相关性分析评估Rab11A表达与免疫特征之间的关系。使用京都基因与基因组百科全书和基因本体分析确定潜在途径。采用免疫组织化学分析、集落形成试验、溴脱氧尿苷掺入试验、免疫荧光和蛋白质印迹法探讨潜在功能和机制。
对TCGA数据库的分析显示,Rab11A在多种癌症中表达显著上调。82.4%的BRCA中Rab11A上调。Rab11A高表达与癌症患者的不良生存相关,是预后不良的预测指标。CIBERSORT分析显示,Rab11A与几乎所有癌症的免疫循环活性评分呈负相关。使用临床BRCA患者的病理样本进一步证实了TCGA-BRCA队列的结果。结果显示,BRCA中Rab11A表达与雌激素受体(ER)和孕激素受体表达相关(p < 0.05)。Rab11A的敲低和过表达影响BRCA细胞的增殖。进一步的机制研究表明,雌激素受体α(ERα)的下调和雌激素受体β(ERβ)的上调介导了Rab11A诱导的BRCA细胞增殖抑制。
Rab11A在泛癌中的表达与预后不良和免疫特征相关。特别是在BRCA中,Rab11A表达通过靶向ERα和ERβ调节细胞增殖。Rab11A高表达与免疫特征、肿瘤微环境和基因突变密切相关。这些结果为探索Rab11A在泛癌中的作用提供了参考,为揭示BRCA潜在治疗靶点提供了新的视角。