Amplification of heterogeneous nuclear ribonucleoprotein A/B aids in immune infiltration regulation and breast cancer tumorigenesis.

IF 2.3
Experimental and therapeutic medicine Pub Date : 2026-05-27 eCollection Date: 2026-07-01 DOI:10.3892/etm.2026.13193
Jiachao Xu, Qian Han, Libin Chen, Min Yang, Jun Huang, Shanhong Lin, Shengmin Zhang
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Abstract

Breast carcinoma ranks among the most prevalent malignant tumors affecting women worldwide. The discovery of biomarkers is important in the diagnosis of breast cancer and the prediction of clinical outcomes in afflicted patients. Heterogeneous nuclear ribonucleoprotein (HNRNP)-AB belongs to the extensive HNRNP superfamily; however, its exact role in the progression of breast carcinoma has not yet been fully clarified. The present study drew upon breast cancer sample datasets retrieved from The Cancer Genome Atlas and Human Protein Atlas databases to examine the expression patterns and prognosis-associated data of HNRNPAB in clinical specimens. Reverse transcription-quantitative PCR was employed to validate the efficiency of HNRNPAB knockdown in breast cancer cell lines. Transwell assays and Cell Counting Kit-8 tests further demonstrated alterations in migratory, invasive and proliferative capacities following small interfering RNA-mediated HNRNPAB knockdown. Bioinformatics was utilized to investigate numerous aspects of HNRNPAB in cancerous tissues, including its mRNA expression profile, prognostic value, signaling pathway remodeling, interaction with cancer stem cells and regulatory effects on the tumor immune microenvironment, as well as immunotherapeutic responses. Compared with normal breast tissues, HNRNPAB exhibited elevated expression in breast cancer tissues, upregulation that appeared to be associated with overall survival outcomes, sex characteristics, lymph node metastasis staging and adverse prognostic profiles in patients. Functionally, HNRNPAB depletion was found to suppress the proliferative activity, migratory potential and invasive capabilities of breast cancer cells. Mechanistically, bioinformatics analyses indicated that high HNRNPAB expression was associated with the tumor immune infiltration status in affected individuals. In summary, the present study determined that HNRNPAB exerted a key regulatory effect on the development and progression of breast cancer and therefore its upregulation holds promise as a diagnostic and prognostic marker. In addition, HNRNPAB serves a notable role in cancer immunotherapy, supporting its potential as a novel therapeutic candidate for the early detection and prognostic evaluation of breast cancer.

异质核糖核蛋白A/B的扩增有助于免疫浸润调节和乳腺癌的发生。
乳腺癌是世界范围内影响妇女最普遍的恶性肿瘤之一。生物标志物的发现对于乳腺癌的诊断和患者临床预后的预测具有重要意义。异质核核糖核蛋白(HNRNP)-AB属于广泛的HNRNP超家族;然而,它在乳腺癌进展中的确切作用尚未完全阐明。本研究利用从癌症基因组图谱和人类蛋白质图谱数据库中检索的乳腺癌样本数据集来检查临床标本中HNRNPAB的表达模式和预后相关数据。采用逆转录-定量PCR技术验证HNRNPAB在乳腺癌细胞系中的敲除效果。Transwell试验和细胞计数试剂盒-8测试进一步证明了小干扰rna介导的HNRNPAB敲低后迁移、侵袭和增殖能力的改变。利用生物信息学研究了HNRNPAB在癌组织中的多个方面,包括其mRNA表达谱、预后价值、信号通路重塑、与癌症干细胞的相互作用、对肿瘤免疫微环境的调节作用以及免疫治疗反应。与正常乳腺组织相比,HNRNPAB在乳腺癌组织中的表达升高,其上调似乎与患者的总体生存结局、性别特征、淋巴结转移分期和不良预后相关。在功能上,HNRNPAB缺失被发现抑制乳腺癌细胞的增殖活性、迁移潜力和侵袭能力。从机制上讲,生物信息学分析表明,HNRNPAB的高表达与患者的肿瘤免疫浸润状态有关。综上所述,本研究确定HNRNPAB在乳腺癌的发生和发展中发挥了关键的调节作用,因此其上调有望作为诊断和预后指标。此外,HNRNPAB在癌症免疫治疗中发挥着重要作用,支持其作为乳腺癌早期检测和预后评估的新候选治疗药物的潜力。
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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