| Literature DB >> 27786373 |
Nasha Qiu1, Xiangrui Liu1, Yin Zhong1, Zhuxian Zhou1, Ying Piao1, Lei Miao2, Qianzhi Zhang1, Jianbin Tang1, Leaf Huang2, Youqing Shen1.
Abstract
Selective gene expression in tumors via responsive dissociation of polyplexes triggered by intracellular signals is demonstrated. An esterase-responsive charge-reversal polymer mediates selective gene expression in the cancer cells high in esterases over fibroblasts low in esterase activity. Its gene therapy with the TRAIL suicide gene effectively induces apoptosis of HeLa cells but does not activate fibroblasts to secrete WNT16B, enabling potent cancer gene therapy with few side effects.Entities:
Keywords: cancer gene therapy; charge-reversal polymer; esterase-responsive; fibroblast exempt; intraperitoneal tumors
Mesh:
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Year: 2016 PMID: 27786373 DOI: 10.1002/adma.201603095
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849