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用于食管癌声动力放疗的超声激活纳米氧敏化剂

Ultrasound-activated nano-oxygen sensitizer for sonodynamic-radiotherapy of esophageal cancer.

作者信息

Liu Jiayin, Shi Manru, Zhao Huijia, Bai Xin, Lin Quan, Guan Xin, Wu Bolin, E Mingyan

机构信息

Department of Radiation Oncology, Harbin Medical University Cancer Hospital No. 150, Haping Road, Nangang District Harbin Heilongjiang Province 150081 China

Department of Ultrasound, Harbin Medical University Cancer Hospital No. 150, Haping Road, Nangang District Harbin Heilongjiang Province 150081 China

出版信息

Nanoscale Adv. 2025 Feb 20;7(8):2209-2221. doi: 10.1039/d5na00042d. eCollection 2025 Apr 8.

Abstract

: owing to the intricate nature, variability, and persistent oxygen-deficient environment associated with esophageal cancer (EC) tissues, radiotherapy (RT) sometimes doesn't work as well because some cancer cells can resist the radiation to a certain extent. This can lead to the cancer coming back in the same spot or even making the treatment ineffective. The integration of RT with oxygenation strategies is a common approach in cancer treatment. The advent of oxygen-enhancing sonodynamic therapy (SDT), leveraging the cytotoxic effects of reactive oxygen species (ROS), has garnered significant attention as an innovative approach to inducing cell death. : this study utilized nanobubbles (NBs) containing the acoustic sensitizer indocyanine green (ICG) to create a nanoplatform (ICG@O NBs) that incorporates oxygen-enhanced SDT and RT. Besides, NBs are paired with low-frequency ultrasound (LFUS), known as ultrasound-targeted nano-bubble destruction (UTND), for precise drug release and improved safety. : experimental findings, including JC-1/DCFH-DA assays, demonstrate that ICG@O NBs effectively enhance the performance of both RT and SDT. RNA sequencing (RNA-seq) demonstrated differential expression of mRNA and LncRNA prior to and after co-treatment. KEGG and GO pathway analysis were then conducted for enriching and recognizing target genes and pathways correlated with the sensitivity of RT, which were revealed to be remarkably clustered in RT-associated pathways. : and investigations have indicated significant efficacy of synergistic treatments, highlighting the potential of combining NBs with SDT and RT for managing EC.

摘要

由于食管癌(EC)组织具有复杂的性质、变异性以及持续的缺氧环境,放射疗法(RT)有时效果不佳,因为一些癌细胞能够在一定程度上抵抗辐射。这可能导致癌症在同一部位复发,甚至使治疗无效。将放射疗法与氧合策略相结合是癌症治疗中的常用方法。利用活性氧(ROS)细胞毒性作用的氧增强型声动力疗法(SDT)的出现,作为一种诱导细胞死亡的创新方法已引起广泛关注。本研究利用含有声学敏化剂吲哚菁绿(ICG)的纳米气泡(NBs)构建了一个结合氧增强型SDT和RT的纳米平台(ICG@O NBs)。此外,NBs与低频超声(LFUS)相结合,即超声靶向纳米气泡破坏(UTND),用于精确药物释放并提高安全性。实验结果,包括JC-1/DCFH-DA检测,表明ICG@O NBs有效地增强了RT和SDT的性能。RNA测序(RNA-seq)显示联合治疗前后mRNA和LncRNA的差异表达。随后进行KEGG和GO通路分析,以富集和识别与RT敏感性相关的靶基因和通路,结果显示这些基因和通路在RT相关通路中显著聚集。研究表明联合治疗具有显著疗效,突出了将NBs与SDT和RT联合用于治疗EC的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdeb/11977337/abe82aed9eaf/d5na00042d-s1.jpg

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