核糖核酸
寡核苷酸
癌细胞
基因
DNA
癌症
基因表达
小RNA
生物
分子生物学
癌症研究
计算生物学
生物化学
遗传学
作者
Andrey Giovanni Gomes de Oliveira,Mikhail V. Dubovichenko,A.A. Eldeeb,Joseph Wanjohi,Sofia S. Zablotskaya,Dmitry M. Kolpashchikov
出处
期刊:ChemBioChem
[Wiley]
日期:2021-01-15
卷期号:22 (10): 1750-1754
被引量:8
标识
DOI:10.1002/cbic.202000769
摘要
Oligonucleotide gene therapy (OGT) agents suppress specific mRNAs in cells and thus reduce the expression of targeted genes. The ability to unambiguously distinguish cancer from healthy cells can solve the low selectivity problem of OGT agents. Cancer RNA markers are expressed in both healthy and cancer cells with a higher expression level in cancer cells. We have designed a DNA-based construct, named DNA thresholder (DTh) that cleaves targeted RNA only at high concentrations of cancer marker RNA and demonstrates low cleavage activity at low marker concentrations. The RNA-cleaving activity can be adjusted within one order of magnitude of the cancer marker RNA concentration by simply redesigning DTh. Importantly, DTh recognizes cancer marker RNA, while cleaving targeted RNA; this offers a possibility to suppress vital genes exclusively in cancer cells, thus triggering their death. DTh is a prototype of computation-inspired molecular device for controlling gene expression and cancer treatment.
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