超声增强的丹酚酸F靶向CXCL5抑制肺癌进展:来自体外PC9和H1299模型的见解

IF 2.1 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Chunxia Ding, Ning Tang, Quancheng Zhou, Xianghua Wu, Miaomiao Han
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引用次数: 0

摘要

背景:肺癌仍然是世界范围内癌症相关死亡的主要原因之一,强调迫切需要更有效和有针对性的治疗策略。中医药以其良好的安全性和广泛的药理作用而闻名,为癌症治疗提供了有希望的候选药物。丹参酚酸F (Salvianolic acid F, SAF)是一种从丹参中提取的重要生物活性化合物,具有抗肿瘤的潜力,但其在肺癌中的作用及其机制尚未得到充分的研究。目的:本研究探讨SAF在肺癌中的抗癌作用,并确定超声是否能增强其治疗效果,重点关注CXCL5/Wnt/β-catenin信号轴。方法:用SAF单独或联合超声治疗人非小细胞肺癌细胞株H1299和PC9。分别使用细胞计数试剂盒-8、划伤愈合和transwell试验评估细胞增殖、迁移和侵袭。通过RNA测序分析基因表达变化,并通过实时定量聚合酶链反应和Western blotting进行验证。通过小干扰rna介导的基因沉默进一步证实了CXCL5的功能参与。结果:SAF显著抑制H1299和PC9细胞的增殖、活力和侵袭性。当SAF与超声接触时,这些效果显着增强。转录组学分析显示CXCL5下调,下游Wnt/β-catenin信号介质抑制,包括Wnt5α和β-catenin。CXCL5敲低模拟SAF的抑制作用,并与SAF治疗协同,证实CXCL5/Wnt/β-catenin轴参与观察到的抗肿瘤反应。结论:超声增强给药SAF可通过靶向CXCL5/Wnt/β-catenin通路显著抑制肺癌细胞增殖和转移。这种组合方法代表了一种新颖而有前途的肺癌生物治疗策略,将中药衍生化合物与无创给药技术相结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrasound-Enhanced Delivery of Salvianolic Acid F Targets CXCL5 to Suppress Lung Cancer Progression: Insights from In Vitro PC9 and H1299 Models.

Background: Lung cancer remains one of the leading causes of cancer-related mortality worldwide, highlighting the urgent need for more effective and targeted therapeutic strategies. Traditional Chinese Medicine (TCM), known for its favorable safety profile and broad pharmacological effects, offers promising candidates for cancer treatment. Salvianolic acid F (SAF), a key bioactive compound derived from Salvia miltiorrhiza, has demonstrated antitumor potential, but its role and underlying mechanisms in lung cancer remain inadequately characterized. Objective: This study investigated the anticancer efficacy of SAF in lung cancer and determines whether ultrasound can enhance its therapeutic effects, with a particular focus on the CXCL5/Wnt/β-catenin signaling axis. Methods: Human non-small cell lung cancer cell lines H1299 and PC9 were treated with SAF alone or in combination with ultrasound. Cell proliferation, migration, and invasion were assessed using cell counting kit-8, scratch wound healing, and transwell assays, respectively. Gene expression changes were analyzed using RNA sequencing and validated by quantitative real-time polymerase chain reaction and Western blotting. Functional involvement of CXCL5 was further confirmed through small interfering RNA-mediated gene silencing. Results: SAF significantly inhibited proliferation, motility, and invasiveness of both H1299 and PC9 cells. These effects were markedly enhanced when SAF was delivered in conjunction with ultrasound exposure. Transcriptomic analysis revealed downregulation of CXCL5 and suppression of downstream Wnt/β-catenin signaling mediators, including Wnt5α and β-catenin. CXCL5 knockdown mimicked the inhibitory effects of SAF and synergized with SAF treatment, confirming the involvement of the CXCL5/Wnt/β-catenin axis in the observed antitumor response. Conclusions: Ultrasound-enhanced delivery of SAF significantly impairs lung cancer cell proliferation and metastasis by targeting the CXCL5/Wnt/β-catenin pathway. This combinatorial approach represents a novel and promising biotherapeutic strategy for lung cancer that integrates TCM-derived compounds with noninvasive delivery technologies.

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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
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