Abstract:
:RNA interference (RNAi) is an evolutionary conserved mechanism for specific gene silencing. There are currently numerous cancer therapy clinical trials based on RNAi technology. Using an adenoviral system as a delivery mediator of RNAi, we investigated the therapeutic effects of targeting three genes simultaneously in vitro and in vivo. In this study, we constructed an recombinant adenoviral shRNA expression system as Adv-pEGFP-shVEGF-shTERT-shBcl-xl for multi-genes silencing. Our results showed that the adenoviral vector can achieve above 90% of transfection efficiency and induced obvious apoptosis in CNE-2 cell both in vitro and in vivo compared with targeting the TERT alone or controlled group.
journal_name
Cancer Lettjournal_title
Cancer lettersauthors
Han JB,Tao ZZ,Chen SM,Kong YG,Xiao BKdoi
10.1016/j.canlet.2011.05.028subject
Has Abstractpub_date
2011-10-28 00:00:00pages
162-9issue
2eissn
0304-3835issn
1872-7980pii
S0304-3835(11)00305-3journal_volume
309pub_type
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