He Haodong
Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, Yichang, 443002, China.
College of Basic Medical Science, China Three Gorges University, Yichang, 443002, China.
Discov Oncol. 2025 Jul 7;16(1):1271. doi: 10.1007/s12672-025-03065-2.
Tumor protein p53 target gene 1 (TP53TG1) is a significant long non-coding RNA (lncRNA) located on human chromosome 7q21.12, exhibiting dysregulated expression in several cancer tissues, and operates both as an oncogene and a tumor suppressor. TP53TG1 modulates gene expression by several mechanisms, including "competitive RNA" activity, competitive miRNA binding, control of critical signaling pathways, and facilitation of epigenetic changes. TP53TG1 affects tumor proliferation, migration, invasion, and apoptosis through intricate mechanisms, modifies tumor cells resistance to therapies, influences the tumor immune microenvironment and metabolic reprogramming, and may present various avenues for clinical therapeutic intervention. Notwithstanding considerable advancements in comprehending the molecular function of TP53TG1, some challenges persist, especially regarding the efficient and targeted administration of TP53TG1-based therapeutics. Advanced RNA delivery technologies, including lipid nanoparticles (LNPs), sphingomyelin-based nanosystems, and polymer-based nanocarriers, have demonstrated the capacity to surmount these obstacles. This review aims to clarify the expression pattern of TP53TG1 in 10 malignant tumors, its biological relevance, its potential as a therapeutic target, and its importance in clinical applications, thereby offering a novel perspective on molecular targeting in cancer. In the future, integrating TP53TG1 with conventional medications may augment efficacy, offer personalized treatments, and eventually increase the prognosis for patients with aggressive or drug-resistant cancers.
肿瘤蛋白p53靶基因1(TP53TG1)是一种重要的长链非编码RNA(lncRNA),位于人类染色体7q21.12上,在多种癌症组织中表达失调,兼具癌基因和肿瘤抑制基因的作用。TP53TG1通过多种机制调节基因表达,包括“竞争性RNA”活性、竞争性miRNA结合、关键信号通路的调控以及表观遗传变化的促进。TP53TG1通过复杂的机制影响肿瘤的增殖、迁移、侵袭和凋亡,改变肿瘤细胞对治疗的抗性,影响肿瘤免疫微环境和代谢重编程,并可能为临床治疗干预提供多种途径。尽管在理解TP53TG1的分子功能方面取得了相当大的进展,但仍存在一些挑战,特别是在基于TP53TG1的治疗药物的有效和靶向给药方面。先进的RNA递送技术,包括脂质纳米颗粒(LNP)、基于鞘磷脂的纳米系统和基于聚合物的纳米载体,已显示出克服这些障碍的能力。本综述旨在阐明TP53TG1在10种恶性肿瘤中的表达模式、其生物学相关性、作为治疗靶点的潜力及其在临床应用中的重要性,从而为癌症的分子靶向治疗提供新的视角。未来,将TP53TG1与传统药物相结合可能会提高疗效,提供个性化治疗,并最终改善侵袭性或耐药性癌症患者的预后。