Oncotarget

Research Papers:

Functional repair of p53 mutation in colorectal cancer cells using trans-splicing

Xingxing He, Jiazhi Liao, Fang Liu, Junwei Yan, Jingjun Yan, Haitao Shang, Qian Dou, Ying Chang, Jusheng Lin and Yuhu Song _

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Oncotarget. 2015; 6:2034-2045. https://doi.org/10.18632/oncotarget.2988

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Abstract

Xingxing He1,*, Jiazhi Liao1,*, Fang Liu2, Junwei Yan1, Jingjun Yan1, Haitao Shang3, Qian Dou3, Ying Chang1, Jusheng Lin1 and Yuhu Song3

1 Institute of Liver Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

2 Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

3 Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

* These authors contributed equally to this work

Correspondence:

Yuhu Song, email:

Jusheng Lin, email:

Keywords: colorectal cancer cells, mutant p53, trans-splicing

Received: September 30, 2014 Accepted: December 09, 2014 Published: December 10, 2014

Abstract

Mutation in the p53 gene is arguably the most frequent type of gene-specific alterations in human cancers. Current p53-based gene therapy contains the administration of wt-p53 or the suppression of mutant p53 expression in p53-defective cancer cells. . We hypothesized that trans-splicing could be exploited as a tool for the correction of mutant p53 transcripts in p53-mutated human colorectal cancer (CRC) cells. In this study, the plasmids encoding p53 pre-trans-splicing molecules (PTM) were transfected into human CRC cells carrying p53 mutation. The plasmids carrying p53-PTM repaired mutant p53 transcripts in p53-mutated CRC cells, which resulted in a reduction in mutant p53 transcripts and an induction of wt-p53 simultaneously. Intratumoral administration of adenovirus vectors carrying p53 trans-splicing cassettes suppressed the growth of tumor xenografts. Repair of mutant p53 transcripts by trans-splicing induced cell-cycle arrest and apoptosis in p53-defective colorectal cancer cells in vitro and in vivo. In conclusion, the present study demonstrated for the first time that trans-splicing was exploited as a strategy for the repair of mutant p53 transcripts, which revealed that trans-splicing would be developed as a new therapeutic approach for human colorectal cancers carrying p53 mutation.


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