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开发一种5-氟尿嘧啶修饰的miR-129模拟物作为非小细胞肺癌的治疗药物。

Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer.

作者信息

Hwang Ga-Ram, Yuen John G, Fesler Andrew, Farley Hannah, Haley John D, Ju Jingfang

机构信息

Department of Pathology, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY 11794, USA.

Molecular and Cell Biology Graduate Program, Stony Brook University, Stony Brook, NY 11794, USA.

出版信息

Mol Ther Oncolytics. 2023 Feb 17;28:277-292. doi: 10.1016/j.omto.2023.02.007. eCollection 2023 Mar 16.

Abstract

Lung cancer is the leading cause of cancer-related deaths in the United States with non-small cell lung cancer (NSCLC) accounting for most cases. Despite advances in cancer therapeutics, the 5-year survival rate has remained poor due to several contributing factors, including its resistance to therapeutics. Therefore, there is a pressing need to develop therapeutics that can overcome resistance. Non-coding RNAs, including microRNAs (miRNAs), have been found to contribute to cancer resistance and therapeutics by modulating the expression of several targets involving multiple key mechanisms. In this study, we investigated the therapeutic potential of miR-129 modified with 5-fluorouracil (5-FU) in NSCLC. Our results show that 5-FU modified miR-129 (5-FU-miR-129) inhibits proliferation, induces apoptosis, and retains function as an miRNA in NSCLC cell lines A549 and Calu-1. Notably, we observed that 5-FU-miR-129 was able to overcome resistance to tyrosine kinase inhibitors and chemotherapy in cell lines resistant to erlotinib or 5-FU. Furthermore, we observed that the inhibitory effect of 5-FU-miR-129 can also be achieved in NSCLC cells under vehicle-free conditions. Finally, 5-FU-miR-129 inhibited NSCLC tumor growth and extended survival without toxic side effects Altogether, our results demonstrate the potential of 5-FU-miR-129 as a highly potent cancer therapeutic in NSCLC.

摘要

肺癌是美国癌症相关死亡的主要原因,其中非小细胞肺癌(NSCLC)占大多数病例。尽管癌症治疗取得了进展,但由于包括对治疗耐药在内的多种因素,5年生存率仍然很低。因此,迫切需要开发能够克服耐药性的治疗方法。已发现包括微小RNA(miRNA)在内的非编码RNA通过调节涉及多种关键机制的多个靶点的表达,在癌症耐药性和治疗中发挥作用。在本研究中,我们研究了用5-氟尿嘧啶(5-FU)修饰的miR-129在NSCLC中的治疗潜力。我们的结果表明,5-FU修饰的miR-129(5-FU-miR-129)在NSCLC细胞系A549和Calu-1中抑制增殖、诱导凋亡,并保留miRNA的功能。值得注意的是,我们观察到5-FU-miR-129能够克服对厄洛替尼或5-FU耐药的细胞系对酪氨酸激酶抑制剂和化疗的耐药性。此外,我们观察到在无载体条件下,5-FU-miR-129在NSCLC细胞中也能实现抑制作用。最后,5-FU-miR-129抑制NSCLC肿瘤生长并延长生存期,且无毒性副作用。总之,我们的结果证明了5-FU-miR-129作为一种高效的NSCLC癌症治疗药物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f751/9995506/f58661df83d8/fx1.jpg

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