TY - JOUR
T1 - A gene-delivery system specific for hepatoma cells and an intracellular kinase signal based on human liver-specific bionanocapsules and signal-responsive artificial polymer
AU - Oishi, Jun
AU - Jung, Joohee
AU - Tsuchiya, Akira
AU - Toita, Riki
AU - Kang, Jeong Hun
AU - Mori, Takeshi
AU - Niidome, Takuro
AU - Tanizawa, Katsuyuki
AU - Kuroda, Shun'ichi
AU - Katayama, Yoshiki
N1 - Funding Information:
This work was financially supported by CREST, the Japan Science Corp., a grant-in-aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture in Japan, and a grant-in-aid for Scientific Research from the Ministry of Health, Labor, and Welfare. J.O. thanks JSPS for the DC scholarship.
PY - 2010/8
Y1 - 2010/8
N2 - Recently, our group has proposed a novel gene-regulation system responding to cAMP-dependent protein kinase (PKA) that has been applied to living cells. In this study, human liver-specific bionanocapsules (BNCs) are used as a gene-delivery system to increase transfection efficiency and to target specific cell types. BNCs can efficiently deliver a target gene to human hepatocytes and hepatoma cells in vitro or in vivo. The combination of a signal-responsive gene-delivery system with BNCs led to an increase in the transfection efficiency and selectivity for hepatoma cells. Expression from the delivered gene was identified from PKA-activated hepatoma cells (HepG2), but not from colon tumor cells (WiDr). These results show that the combination of a gene-regulation system responding to an intracellular signal with BNC can be used for the selective treatment of human hepatoma cells.
AB - Recently, our group has proposed a novel gene-regulation system responding to cAMP-dependent protein kinase (PKA) that has been applied to living cells. In this study, human liver-specific bionanocapsules (BNCs) are used as a gene-delivery system to increase transfection efficiency and to target specific cell types. BNCs can efficiently deliver a target gene to human hepatocytes and hepatoma cells in vitro or in vivo. The combination of a signal-responsive gene-delivery system with BNCs led to an increase in the transfection efficiency and selectivity for hepatoma cells. Expression from the delivered gene was identified from PKA-activated hepatoma cells (HepG2), but not from colon tumor cells (WiDr). These results show that the combination of a gene-regulation system responding to an intracellular signal with BNC can be used for the selective treatment of human hepatoma cells.
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U2 - 10.1016/j.ijpharm.2010.06.012
DO - 10.1016/j.ijpharm.2010.06.012
M3 - Article
C2 - 20558262
AN - SCOPUS:77955054321
SN - 0378-5173
VL - 396
SP - 174
EP - 178
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
IS - 1-2
ER -