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Adenovirus-mediated anti-AEG-1 ScFv expression driven by stathmin promoter inhibits tumor growth in cervical cancer.


ABSTRACT: Background:Astrocyte-elevated gene-1 (AEG-1) is over-expressed in many cancer cells and has multiple key functions in tumor initiation and progression. Currently, targeted-AEG-1 siRNA is one of the most common techniques to down-regulate AEG-1 expression, but the lack of tumor specificity and available delivery system make it difficult to enter clinical trials. Methods:In this study, we creatively developed an adenovirus-mediated anti-AEG-1 single-chain antibody fragment (ScFv) expression system driven by a tumor specific promoter, and experimented with it in human cervical carcinoma cells to investigate the effect on tumor's proliferation and apoptosis. Results:The results showed that of HeLa and SiHa cells treated with this recombinant anti-AEG-1 ScFv adenovirus not only inhibited cell growth, but induced apoptosis both in vitro and in vivo. Furthermore, we also observed that the expressions of several apoptosis-related genes like Akt 1 and c-Myc decreased, while NF-?B (p65) and cleaved caspase 3 increased on protein levels in vivo. Conclusion:We concluded that stathmin promoter-driving anti-AEG-1 ScFv adenoviral system may be a breakthrough for its dual-specificity, and serve as an adjuvant tumor specific therapy method in the treatment for human cervical cancers.

SUBMITTER: Long M 

PROVIDER: S-EPMC7068931 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

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Adenovirus-mediated anti-AEG-1 ScFv expression driven by stathmin promoter inhibits tumor growth in cervical cancer.

Long Min M   Lin Fang F   Wang Xi X   Chen Xi X   Liu Li L   Zhang Huizhong H   Dong Ke K  

Cancer cell international 20200312


<h4>Background</h4><i>Astrocyte</i>-<i>elevated gene</i>-<i>1 (AEG</i>-<i>1)</i> is over-expressed in many cancer cells and has multiple key functions in tumor initiation and progression. Currently, targeted-AEG-1 siRNA is one of the most common techniques to down-regulate AEG-1 expression, but the lack of tumor specificity and available delivery system make it difficult to enter clinical trials.<h4>Methods</h4>In this study, we creatively developed an adenovirus-mediated anti-AEG-1 single-chain  ...[more]

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