Ser Archer (Talk | contribs) |
Ser Archer (Talk | contribs) |
||
Line 168: | Line 168: | ||
<div id="words" style="position:relative;display:none;width:80%;top:43%;margin-left:10%;font-size:2.2rem;line-height:2.5;"> | <div id="words" style="position:relative;display:none;width:80%;top:43%;margin-left:10%;font-size:2.2rem;line-height:2.5;"> | ||
<h1 style="position:relative;width:90%;margin-left:5%;top:28%;text-align:center;">A gene therapy strategy to target hepatocellular carcinoma based on conditional RNA interference</h1> | <h1 style="position:relative;width:90%;margin-left:5%;top:28%;text-align:center;">A gene therapy strategy to target hepatocellular carcinoma based on conditional RNA interference</h1> | ||
− | <h4 style="font-size:2rem;line-height:2">MicroRNA(miRNA) is a short non-coding RNA, which has the ability to target mRNA and | + | <h4 style="font-size:2rem;line-height:2">MicroRNA(miRNA) is a short non-coding RNA, which has the ability to target mRNA and mediate its degradation to downgrade gene expression at transcription level. This mediation effect is called post-transcriptional gene silencing (PTGS, which is also know as RNA interference). RNA interference(RNAi) has proved its potential as gene therapy. The mature miRNA are cleaved from pri-miRNA which gives us possibility to make it conditional. An “AND” gate system based on specific promoters and RNA-dependent RNA polymerase(RdRp) was designed to avoid undesirable effects due to low selectivity. Together, they formed our conditional RNA gene therapy. This year, CPU_CHINA is focusing on hepatocellular carcinoma (HCC). But significantly, the promoters and the target here can be replaced with other disease-specific promoters and target, in gene therapy for the corresponding diseases which enables our project to be a remarkable novel application.</h4> |
</div> | </div> | ||
Revision as of 10:26, 7 December 2018