作者: Xinbo Huang , Chengle Zhuang , Changshui Zhuang , Tiefu Xiong , Yawen Li
DOI: 10.1039/C7MB00354D
关键词:
摘要: The current therapies for treating tumors are lacking in efficacy and specificity. Synthetic biology principles may bring some new possible methods curing cancer. Here we present a synthetic logic circuit based on the CRISPR/Cas9 system. technology has been applied many biological fields, including cancer research. In this study, expression of Cas9 nuclease was controlled indirectly by an enhanced hTERT promoter using GAL4/upstream activating sequence (UAS) binding driven 5XUAS, single guide RNA (sgRNA) used to target mutant or wild-type HRAS, fusion gene GAL4-P65 promoter. system tested bladder cells (T24 5637) results showed that could drive these cell lines. Then all devices were packed into lentivirus quantitative real-time PCR mRNA level HRAS selectively inhibited T24 5637 cells. functional experiments suggested proliferation, migration invasion suppressed, apoptosis rate increased but not human foreskin fibroblasts (HFF). conclusion, successfully constructed promoter-driven data it suppress progression