Lu Yuan, Wang Yuan, Zhang Mi, Liu Li, Li Fakai, Zhang Jian, Ye Mingxiang, Zhao Hu, Zhao Jing, Yan Bo, Yang Angang, Zhang Rui, Li Xia, Ren Xinling
Department of Respiratory Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Department of Respiratory Medicine, PLA General Hospital, Beijing, China.
Oncotarget. 2016 Apr 26;7(17):23594-607. doi: 10.18632/oncotarget.8053.
Overexpression of human epidermal growth factor receptor type2 (HER2) is closely associated with aggressive progression and poor prognosis in non-small cell lung cancer (NSCLC). Here, we generated an EGFR-scFv-arginine nonamer peptide fusion protein (scFv-9R) as a cargo to deliver HER2 specific siRNA into HER2-positive NSCLC cells both in vitro and in vivo. HER2-siRNAs delivered by scFv-9R effeciently silenced HER2 expression in EGFR-positive NSCLC cells, and consequently resulted in G1 arrest and cell growth inhibition. Importantly, intravenous injection of scFv-9R/HER2-siRNA complex markedly suppressed growth of EGFR-positive NSCLC xenograft in nude mice, resulting from downregulated HER2 expression, reduced cell proliferation and enhanced cell apoptosis. Collectively, our study provides a novel therapeutic strategy for the treatment of EGFR-positive, HER2-overexpressed NSCLC.
人表皮生长因子受体2(HER2)的过表达与非小细胞肺癌(NSCLC)的侵袭性进展和不良预后密切相关。在此,我们构建了一种EGFR单链抗体片段-精氨酸九聚体肽融合蛋白(scFv-9R)作为载体,在体外和体内将HER2特异性小干扰RNA(siRNA)递送至HER2阳性NSCLC细胞中。由scFv-9R递送的HER2-siRNAs有效沉默了EGFR阳性NSCLC细胞中的HER2表达,进而导致G1期阻滞和细胞生长抑制。重要的是,静脉注射scFv-9R/HER2-siRNA复合物显著抑制了裸鼠体内EGFR阳性NSCLC异种移植瘤的生长,这是由于HER2表达下调、细胞增殖减少和细胞凋亡增强所致。总之,我们的研究为治疗EGFR阳性、HER2过表达的NSCLC提供了一种新的治疗策略。