Thankachan Sanu, Kavitha K P, Eswaran Sangavi, Kabekkodu Shama Prasada, Suresh Padmanaban S
Department of Bioscience and Engineering, National Institute of Technology, Calicut 673601 Kerala, India.
Department of Pathology, Aster Malabar Institute of Medical Sciences (MIMS), Calicut 673016 Kerala, India.
Gene. 2025 Sep 10;964:149638. doi: 10.1016/j.gene.2025.149638. Epub 2025 Jun 19.
Worldwide, breast cancer is the most frequent cancer in women. Current research reveals that lncRNA/miRNA/mRNA axes are involved in several cancers. The lncRNA NEAT1 sponging of miR-20b-5p and STAT3 regulation by miR-20b-5p have previously been established. The clinicopathological relationship between NEAT1 and the miR-20b-5p/STAT3 axis in breast cancers is unknown. This study aims to investigate the clinicopathological associations and significance of NEAT1/miR-20b-5p/STAT3 axes in breast cancer. qRT-PCR and immunohistochemistry were performed on archived formalin-fixed paraffin-embedded breast tumor tissues (n = 79) and adjacent normal tissues (n = 40). Receiver operating characteristic (ROC) curve analysis examined NEAT1 and miR-20b-5p diagnostic value. The qRT-PCR revealed significantly higher total NEAT1 and NEAT1_2 isoform levels in breast tumors compared to normal tissues with significant associations with ER, PR statuses, age, stages, and lymph node metastasis (p < 0.05). Methylation-specific PCR of DNA showed that normal and tumor samples had distinct NEAT1 promoter methylation (p < 0.05). Immunohistochemistry showed that tumors and normal tissues have differing STAT3 protein expression, and significantly correlated with NEAT1 levels (p < 0.05). Bioinformatics analysis predicted STAT3 targeting hsa-miR-20b-5p and substantial NEAT1_2 isoform interaction with hsa-miR-20b-5p. qRT-PCR revealed low levels of hsa-miR-20b-5p and an inverse correlation with NEAT1 and NEAT1_2 levels in tumors (p < 0.05). NEAT1 and miR-20b-5p have diagnostic values according to ROC curves. Knockdown of NEAT1 in MCF7 cells by siRNA increased hsa-miR-20b-5p levels and decreased STAT3 mRNA. CCND1 expression correlated with the expression of its transcriptional activator STAT3 in MCF7 cells and tumor tissues. Overall, the study suggests NEAT1/hsa-miR-20b-5p/STAT3 axes as a potential biomarker in breast tumors.
在全球范围内,乳腺癌是女性中最常见的癌症。当前研究表明,lncRNA/miRNA/mRNA轴与多种癌症有关。此前已证实lncRNA NEAT1可吸附miR-20b-5p并通过miR-20b-5p调节STAT3。乳腺癌中NEAT1与miR-20b-5p/STAT3轴之间的临床病理关系尚不清楚。本研究旨在探讨NEAT1/miR-20b-5p/STAT3轴在乳腺癌中的临床病理关联及意义。对存档的福尔马林固定石蜡包埋乳腺肿瘤组织(n = 79)和相邻正常组织(n = 40)进行qRT-PCR和免疫组织化学检测。通过受试者工作特征(ROC)曲线分析评估NEAT1和miR-20b-5p的诊断价值。qRT-PCR结果显示,与正常组织相比,乳腺肿瘤中NEAT1总量和NEAT1_2亚型水平显著更高,且与雌激素受体(ER)、孕激素受体(PR)状态、年龄、分期及淋巴结转移显著相关(p < 0.05)。DNA甲基化特异性PCR显示,正常样本和肿瘤样本的NEAT1启动子甲基化情况不同(p < 0.05)。免疫组织化学显示,肿瘤组织和正常组织的STAT3蛋白表达不同,且与NEAT1水平显著相关(p < 0.05)。生物信息学分析预测STAT3靶向hsa-miR-20b-5p,且NEAT1_2亚型与hsa-miR-20b-5p存在大量相互作用。qRT-PCR显示肿瘤中hsa-miR-20b-5p水平较低,且与NEAT1和NEAT1_2水平呈负相关(p < 0.05)。根据ROC曲线,NEAT1和miR-20b-5p具有诊断价值。通过小干扰RNA(siRNA)敲低MCF7细胞中的NEAT1可提高hsa-miR-20b-5p水平并降低STAT3 mRNA水平。在MCF7细胞和肿瘤组织中,细胞周期蛋白D1(CCND1)表达与其转录激活因子STAT3的表达相关。总体而言,该研究表明NEAT1/hsa-miR-20b-5p/STAT3轴可能是乳腺肿瘤中的一种生物标志物。