Flores-Estrada José Javier, Jiménez Adriana, Victoria-Acosta Georgina, Cortés-Malagón Enoc Mariano, Ortiz-López María Guadalupe, Alvarez-Sánchez María Elizbeth, Nuñez-Olvera Stephanie I, Pérez-Navarro Yussel Fernando, Morales-Reyna Marcos, Puente-Rivera Jonathan
División de Investigación, Hospital Juárez De México, Mexico City 07760, Mexico.
Genetics Laboratory, Hospital Nacional Homeopático, Mexico City 06800, Mexico.
Int J Mol Sci. 2025 Jul 29;26(15):7340. doi: 10.3390/ijms26157340.
Nuclear receptors (NRs) are ligand-activated transcription factors that regulate gene expression and are involved in diverse physiological and pathological processes, including carcinogenesis. In bladder cancer (BCa), dysregulation of NR signaling pathways has been linked to tumor initiation, progression, therapy resistance, and immune evasion. Recent evidence highlights the intricate crosstalk between NRs and microRNAs (miRNAs), which are small non-coding RNAs that posttranscriptionally modulate gene expression. This review provides an integrated overview of the molecular interactions between key NRs and miRNAs in BCa. We investigated how miRNAs regulate NR expression and function and, conversely, how NRs influence miRNA biogenesis, thereby forming regulatory feedback loops that shape tumor behavior. Specific miRNA-NR interactions affecting epithelial-to-mesenchymal transition, metabolic reprogramming, angiogenesis, and chemoresistance are discussed in detail. Additionally, we highlight therapeutic strategies targeting NR-miRNA networks, including selective NR modulators, miRNA mimics and inhibitors, as well as RNA-based combinatorial approaches focusing on their utility as diagnostic biomarkers and personalized treatment targets. Understanding the molecular complexity of NR-miRNA regulation in BCa may open new avenues for improving therapeutic outcomes and advancing precision oncology in urological cancers.
核受体(NRs)是配体激活的转录因子,可调节基因表达,并参与包括致癌作用在内的多种生理和病理过程。在膀胱癌(BCa)中,NR信号通路的失调与肿瘤的发生、进展、治疗耐药性和免疫逃逸有关。最近的证据突显了核受体与微小RNA(miRNAs)之间复杂的相互作用,微小RNA是一类小的非编码RNA,可在转录后调节基因表达。本综述全面概述了BCa中关键核受体与微小RNA之间的分子相互作用。我们研究了微小RNA如何调节核受体的表达和功能,反之,核受体如何影响微小RNA的生物合成,从而形成塑造肿瘤行为的调节反馈回路。详细讨论了影响上皮-间质转化、代谢重编程、血管生成和化疗耐药性的特定微小RNA-核受体相互作用。此外,我们强调了针对核受体-微小RNA网络的治疗策略,包括选择性核受体调节剂、微小RNA模拟物和抑制剂,以及基于RNA的联合方法,重点介绍了它们作为诊断生物标志物和个性化治疗靶点的效用。了解BCa中核受体-微小RNA调节的分子复杂性可能为改善治疗效果和推进泌尿系统癌症的精准肿瘤学开辟新途径。