pNaktide逆转atp1a1缺乏症透明细胞肾细胞癌的代谢重编程和疾病进展。

IF 5 3区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yinghong Zhao, Jialing Lv, Wen Zhang, Ruoyu Deng, Chunyan Li, Lin Wang, Tengfei Zhang, Feineng Liu, Kaili Ma, Zhengcun Wu, Chao Zhang
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引用次数: 0

摘要

据报道,ATP1A1在各种肿瘤中表现出差异表达;然而,其在透明细胞肾细胞癌(ccRCC)中的具体作用尚不清楚。本研究探讨了ATP1A1在ccRCC中的作用,评估了其作为预后标志物和治疗靶点的潜力。通过数据库分析和临床样本评估,我们发现ATP1A1在ccRCC中表达显著下调,且与患者预后不良密切相关。体外和体内实验进一步证实了ATP1A1通过抑制SRC激酶活性发挥肿瘤抑制作用。此外,共表达基因分析表明,ATP1A1可能通过靶向代谢重编程来调节ccRCC的发育。我们还发现,ATP1A1的过表达诱导糖酵解向氧化磷酸化(OXPHOS)的代谢转变,导致活性氧(ROS)水平升高和随后的细胞凋亡。此外,我们评估了pNaktide的治疗潜力,pNaktide是一种模拟ATP1A1功能的肽。我们的研究表明,pNaktide通过抑制SRC信号通路和诱导类似于ATP1A1过表达的代谢变化,有效地抑制体外和体内ccRCC的增殖。利用裸鼠模型的研究进一步证实,pNaktide可显著降低肿瘤体积和重量,支持其作为治疗药物的潜力。总之,本研究表明,ATP1A1低表达是ccRCC进展的关键因素,而pNaktide通过恢复ATP1A1样功能,为ccRCC提供了一种有希望的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
pNaktide reverses metabolic reprogramming and disease progression of ATP1A1-deficiency clear cell renal cell carcinoma.

ATP1A1 has been reported to exhibit differential expression across various tumors; however, its specific role in clear cell renal cell carcinoma (ccRCC) remains uncharted. This study investigates the role of ATP1A1 in ccRCC, assessing its potential as a prognostic marker and therapeutic target. Through database analysis and clinical sample evaluation, we found that ATP1A1 expression is significantly downregulated in ccRCC and closely correlates with poor patient prognosis. Both in vitro and in vivo experiments further confirmed that ATP1A1 exerts tumor-suppressive effects by inhibiting SRC kinase activity. Additionally, co-expression gene analysis suggests that ATP1A1 may regulate ccRCC development by targeting metabolic reprogramming. We also discovered that the overexpression of ATP1A1 induces a metabolic shift from glycolysis to oxidative phosphorylation (OXPHOS), resulting in increased levels of reactive oxygen species (ROS) and subsequent apoptosis. Moreover, we evaluated the therapeutic potential of pNaktide, a peptide that mimics ATP1A1 function. Our research indicates that pNaktide effectively inhibits ccRCC proliferation both in vitro and in vivo by suppressing the SRC signaling pathway and inducing metabolic changes akin to those observed with ATP1A1 overexpression. Studies utilizing nude mouse models further confirmed that pNaktide significantly reduces tumor volume and weight, supporting its potential as a therapeutic agent. In summary, this study demonstrates that low ATP1A1 expression is a critical factor in ccRCC progression and that pNaktide, by restoring ATP1A1-like functions, presents a promising therapeutic strategy for ccRCC.

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来源期刊
Cancer gene therapy
Cancer gene therapy 医学-生物工程与应用微生物
CiteScore
10.20
自引率
0.00%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Cancer Gene Therapy is the essential gene and cellular therapy resource for cancer researchers and clinicians, keeping readers up to date with the latest developments in gene and cellular therapies for cancer. The journal publishes original laboratory and clinical research papers, case reports and review articles. Publication topics include RNAi approaches, drug resistance, hematopoietic progenitor cell gene transfer, cancer stem cells, cellular therapies, homologous recombination, ribozyme technology, antisense technology, tumor immunotherapy and tumor suppressors, translational research, cancer therapy, gene delivery systems (viral and non-viral), anti-gene therapy (antisense, siRNA & ribozymes), apoptosis; mechanisms and therapies, vaccine development, immunology and immunotherapy, DNA synthesis and repair. Cancer Gene Therapy publishes the results of laboratory investigations, preclinical studies, and clinical trials in the field of gene transfer/gene therapy and cellular therapies as applied to cancer research. Types of articles published include original research articles; case reports; brief communications; review articles in the main fields of drug resistance/sensitivity, gene therapy, cellular therapy, tumor suppressor and anti-oncogene therapy, cytokine/tumor immunotherapy, etc.; industry perspectives; and letters to the editor.
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