Hossain Fokhrul, Gonzalez-Ramirez Martha I, Garai Jone, Polania-Villanueva Diana, Li Li, Nafees Farzeen, Manirujjaman Md, Liu Bolin, Majumder Samarpan, Wu Xiao-Cheng, Hicks Chindo, Del Valle Luis, Danos Denise, Ochoa Augusto, Miele Lucio, Zabaleta Jovanny
Department of Genetics, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.
Center for Biomedical Informatics and Genomics, School of Medicine, Tulane University, New Orleans, LA 70112, USA.
Int J Mol Sci. 2025 Sep 18;26(18):9101. doi: 10.3390/ijms26189101.
Triple-negative breast cancer (TNBC) is an aggressive, heterogeneous subtype of breast cancer. miRNAs play an essential role in TNBC pathogenesis and prognosis. Obesity is linked with an increased risk for several cancers, including breast cancer. Obesity is also related to the dysregulation of miRNA expression in adipose tissues. However, there is limited knowledge about race- and obesity-specific differential miRNA expression in TNBC. We performed miRNA sequencing of 48 samples (24 tumor and 24 adjacent non-tumor tissues) and RNA sequencing of 24 tumors samples from Black (AA) and White (EA) TNBC patients with or without obesity. We identified 55 miRNAs exclusively associated with tumors in obese EA patients and 33 miRNAs in obese AA patients, each capable of distinguishing tumor tissues from obese from lean individuals within their respective racial groups. In EA, we detected 41 significant miRNA-mRNA correlations. Notably, miR-181b-5p and miR-877-5p acted as negative regulators of tumor-suppressor genes (e.g., , , ), while miR-204-5p and miR-143-3p appeared to indirectly target oncogenes (e.g., , , , ). Among AA patients, we found 28 significant miRNA-mRNA interactions. miR-195-5p, miR-130a-3p, miR-130a-5p, miR-424-5p, miR-148a-3p, miR-374-5p, and miR-30a-5p each potentially downregulated two or more genes (e.g., , , , , ). Pathway enrichment analysis highlighted , , , , , and as the most commonly differentially expressed in EA, whereas , , and were most frequently in AA. These findings highlight the importance of considering race-specific miRNA-mRNA signatures in understanding TNBC in the context of obesity, offering insights into biomarker-driven patient stratification for targeted therapeutic strategies.
三阴性乳腺癌(TNBC)是一种侵袭性、异质性的乳腺癌亚型。微小RNA(miRNA)在TNBC的发病机制和预后中起着至关重要的作用。肥胖与包括乳腺癌在内的多种癌症风险增加有关。肥胖还与脂肪组织中miRNA表达失调有关。然而,关于TNBC中种族和肥胖特异性的miRNA差异表达的了解有限。我们对48个样本(24个肿瘤组织和24个相邻非肿瘤组织)进行了miRNA测序,并对24个肿瘤样本进行了RNA测序,这些样本来自有或没有肥胖的黑人(AA)和白人(EA)TNBC患者。我们在肥胖的EA患者中鉴定出55个仅与肿瘤相关的miRNA,在肥胖的AA患者中鉴定出33个miRNA,它们各自能够在其各自种族群体中区分肥胖个体与瘦个体的肿瘤组织。在EA中,我们检测到41个显著的miRNA - mRNA相关性。值得注意的是,miR - 181b - 5p和miR - 877 - 5p作为肿瘤抑制基因(如 、 、 )的负调节因子,而miR - 204 - 5p和miR - 143 - 3p似乎间接靶向癌基因(如 、 、 、 )。在AA患者中,我们发现28个显著的miRNA - mRNA相互作用。miR - 195 - 5p、miR - 130a - 3p、miR - 130a - 5p、miR - 424 - 5p、miR - 148a - 3p、miR - 374 - 5p和miR - 30a - 5p各自可能下调两个或更多基因(如 、 、 、 、 )。通路富集分析突出显示 、 、 、 、 、 和 在EA中差异表达最常见,而 、 、 和 在AA中最常见。这些发现突出了在肥胖背景下理解TNBC时考虑种族特异性miRNA - mRNA特征的重要性,为基于生物标志物的患者分层以制定靶向治疗策略提供了见解。