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10.1016/j.ymthe.2017.04.005

http://scihub22266oqcxt.onion/10.1016/j.ymthe.2017.04.005
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C5498809!5498809!28457664
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suck abstract from ncbi


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pmid28457664      Mol+Ther 2017 ; 25 (7): 1588-95
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  • In Vivo Delivery and Therapeutic Effects of a MicroRNA on Colorectal Liver Metastases #MMPMID28457664
  • Oshima G; Guo N; He C; Stack ME; Poon C; Uppal A; Wightman SC; Parekh A; Skowron KB; Posner MC; Lin W; Khodarev NN; Weichselbaum RR
  • Mol Ther 2017[Jul]; 25 (7): 1588-95 PMID28457664show ga
  • Multiple therapeutic agents are typically used in concert to effectively control metastatic tumors. Recently, we described microRNAs that are associated with the oligometastatic state, in which a limited number of metastatic tumors progress to more favorable outcomes. Here, we report the effective delivery of an oligometastatic microRNA (miR-655-3p) to colorectal liver metastases using nanoscale coordination polymers (NCPs). The NCPs demonstrated a targeted and prolonged distribution of microRNAs to metastatic liver tumors. Tumor-targeted microRNA miR-655-3p suppressed tumor growth when co-delivered with oxaliplatin, suggesting additive or synergistic interactions between microRNAs and platinum drugs. This is the first known example of systemically administered nanoparticles delivering an oligometastatic microRNA to advanced metastatic liver tumors and demonstrating tumor-suppressive effects. Our results suggest a potential therapeutic strategy for metastatic liver disease by the co-delivery of microRNAs and conventional cytotoxic agents using tumor-specific NCPs.
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