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脂质包覆的阿霉素-碳酸钙纳米粒递送的 miR-375 克服了肝癌的化疗耐药性。

MiR-375 delivered by lipid-coated doxorubicin-calcium carbonate nanoparticles overcomes chemoresistance in hepatocellular carcinoma.

机构信息

School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Institute of Liver Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, China.

School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Nanomedicine. 2017 Nov;13(8):2507-2516. doi: 10.1016/j.nano.2017.05.010. Epub 2017 Jun 1.

Abstract

Hepatocellular carcinoma (HCC) is a prevalent and lethal disease that is characterized by drug resistance. Doxorubicin (DOX) is a widely used chemotherapeutic drug and miR-375 has been shown to be a tumor suppressor in HCC. Here, we reported that miR-375 and DOX co-loaded into lipid-coated calcium carbonate nanoparticles (LCC-DOX/miR-375 NPs), enhanced the anti-tumor effects through combination therapy, and were highly effective in reversing drug resistance in HCC. LCC-DOX/miR-375 NPs were prepared by a reverse microemulsions method. In vitro, LCC-DOX/miR-375 NPs exhibited enhanced intracellular accumulation, pH-sensitive DOX release and potent cytotoxicity. In vivo, LCC-DOX/miR-375 NPs showed efficient antitumor effect both in xenograft and primary HCC murine models. Our results showed that the LCC-DOX/miR-375 nanoparticles provide a novel strategy to overcome the drug resistance and promote addictive effect between miR-375 and DOX in HCC.

摘要

肝细胞癌 (HCC) 是一种常见且致命的疾病,其特征是耐药性。阿霉素 (DOX) 是一种广泛使用的化疗药物,已有研究表明 miR-375 是 HCC 的肿瘤抑制因子。在这里,我们报道了将 miR-375 和 DOX 共同装载到脂质包覆碳酸钙纳米粒子 (LCC-DOX/miR-375 NPs) 中,通过联合治疗增强了抗肿瘤作用,并在逆转 HCC 耐药性方面具有很高的疗效。LCC-DOX/miR-375 NPs 通过反相微乳液法制备。体外,LCC-DOX/miR-375 NPs 表现出增强的细胞内积累、pH 敏感的 DOX 释放和强大的细胞毒性。在体内,LCC-DOX/miR-375 NPs 在异种移植和原发性 HCC 小鼠模型中均表现出有效的抗肿瘤作用。我们的研究结果表明,LCC-DOX/miR-375 纳米粒子为克服耐药性和促进 miR-375 和 DOX 之间的协同作用提供了一种新策略。

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