Data from An Artificially Designed Interfering lncRNA Expressed by Oncolytic Adenovirus Competitively Consumes OncomiRs to Exert Antitumor Efficacy in Hepatocellular Carcinoma

作者：Xiaoya Li, Yinghan Su, Bin Sun, Weidan Ji, Zhangxiao Peng, Yang Xu, Mengchao Wu, Changqing Su · 年份：2023 · DOI：10.1158/1535-7163.c.6538869.v1 · 研究领域：Virus-based gene therapy research、Cancer Research and Treatments、Viral gastroenteritis research and epidemiology

<div>Abstract<p>Endogenous miRNAs, especially oncogenic miRNAs (OncomiR), have been molecular targets for cancer therapy. We generated an artificially designed interfering long noncoding RNA (lncRNAi), which contains the sequences that can complementarily bind to multiple OncomiRs and is expressed by cancer-selectively replicating adenovirus. The adenovirus-expressed lncRNAi with high levels in hepatocellular carcinoma (HCC) cells competes with OncomiR target genes to bind to and consume OncomiRs, thereby achieving the targeted anti-HCC efficacy. With the targeting replication of adenovirus in HCC cells, lncRNAi was highly expressed and resulted in decreased abilities of proliferation, migration, and invasion, induced cell-cycle changes and apoptosis, and markedly changed the cellular mRNA and miRNA expression profiles in HCC cells. The optimal antitumor effect was also demonstrated on HCC cell line xenograft models and HCC patient–derived xenograft (PDX) tumor models in nude mice. This strategy has established a technology platform with a reliable therapeutic effect for HCC therapy. <i>Mol Cancer Ther; 15(7); 1436–51. ©2016 AACR</i>.</p></div>