Targeting Snail1 by CRISPR/Cas9 System Inhibits the Proliferation and Migration of Human Gastric Cancer Cells

Peng-Wei Zhang, Zhehang Chen, Zhi Shi
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Abstract

The zinc-finger transcriptional repressor Snail1 affects cancer progression by controlling the epithelial cell-mesenchymal transition. The RNA-guided clustered regularly interspaced short palindromic (CRISPR) with a CRISPR-associated nuclease 9 (Cas9) nuclease system has been extensively used for gene editing. Here, we used two distinct sgRNAs to successfully target Snail1 in the gastric cancer cell line MGC803 with the CRISPR/Cas9 system. Furthermore, we discovered that Snail1 knockout reduced the proliferation and migration of MGC803 cells.
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CRISPR/Cas9系统靶向Snail1抑制人胃癌细胞增殖和迁移
锌指转录抑制因子Snail1通过控制上皮细胞-间充质转化来影响癌症的进展。RNA引导的具有CRISPR相关核酸酶9(Cas9)核酸酶系统的规则间隔短回文簇(CRISPR)已被广泛用于基因编辑。在此,我们使用两种不同的sgRNA,利用CRISPR/Cas9系统成功靶向癌症细胞系MGC803中的Snail1。此外,我们发现Snail1敲除降低了MGC803细胞的增殖和迁移。
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