结直肠癌
体内
癌症
癌症研究
癌细胞
癌症干细胞
转移
医学
转染
体外
生物
细胞培养
内科学
生物化学
遗传学
生物技术
作者
Ning Wu,Andrew Fesler,Hua Liu,Jingfang Ju
出处
期刊:Oncotarget
[Impact Journals, LLC]
日期:2017-11-06
卷期号:9 (10): 8887-8897
被引量:27
标识
DOI:10.18632/oncotarget.22322
摘要
Resistance to 5-Fluorouracil (5-FU) based chemotherapy is the major reason for failure of treating patients with advanced colorectal cancer.In this study, we developed a novel miR-129 mimic with potent efficacy in eliminating resistant colon cancer stem cells both in vitro and in vivo. We integrated 5-FU into miR-129 by replacing Uracil (U) to generate 5-FU-miR-129 mimics (Mimic-1).Mimic-1 is a strong therapeutic candidate with a number of unique features. Mimic-1 can be delivered to cancer cells without any transfection reagents (e.g. lipids, viral vector, nanoparticles). Mimic-1 is more potent at inhibiting cell proliferation and inducing cell cycle arrest at G1 phase than native miR-129 and the other mimics tested, while retaining target specificity. Mimic-1 prevents colon cancer metastasis in vivo without toxicity.This represents a significant advancement in the development of a nontoxic and highly potent miRNA based cancer therapeutics and establishes a foundation for further developing Mimic-1 as a novel anti-cancer therapeutic for treating colorectal cancer.
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