Unknown

Dataset Information

0

An Efficient Light-Inducible P53 Expression System for Inhibiting Proliferation of Bladder Cancer Cell.


ABSTRACT: Optogenetic gene expression systems enable spatial-temporal modulation of gene transcription and cell behavior. Although applications in biomedicine are emerging, the utility of optogenetic gene switches remains elusive in cancer research due to the relative low gene activation efficiency. Here, we present an optimized CRISPR-Cas9-based light-inducible gene expression device that controls gene transcription in a dose-dependent manner. To prove the potential utility of this device, P53 was tested as a functional target in the bladder cancer cell models. It was illustrated that the light-induced P53 inhibited proliferation of 5637 and UMUC-3 cell effectively. The "light-on" gene expression system may demonstrate a novel therapeutic strategy for bladder cancer intervention.

SUBMITTER: Lin F 

PROVIDER: S-EPMC5069448 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

altmetric image

Publications

An Efficient Light-Inducible P53 Expression System for Inhibiting Proliferation of Bladder Cancer Cell.

Lin Fan F   Dong Liang L   Wang Weiming W   Liu Yuchen Y   Huang Weiren W   Cai Zhiming Z  

International journal of biological sciences 20161018 10


Optogenetic gene expression systems enable spatial-temporal modulation of gene transcription and cell behavior. Although applications in biomedicine are emerging, the utility of optogenetic gene switches remains elusive in cancer research due to the relative low gene activation efficiency. Here, we present an optimized CRISPR-Cas9-based light-inducible gene expression device that controls gene transcription in a dose-dependent manner. To prove the potential utility of this device, P53 was tested  ...[more]

Similar Datasets

| S-EPMC7814291 | biostudies-literature
| S-EPMC7710612 | biostudies-literature
| S-EPMC2745301 | biostudies-literature
| S-EPMC3464113 | biostudies-literature
| S-EPMC55510 | biostudies-literature
| S-EPMC7491154 | biostudies-literature
| S-EPMC4741965 | biostudies-literature
| S-EPMC3937721 | biostudies-literature
| S-EPMC9128170 | biostudies-literature
| S-EPMC9033812 | biostudies-literature