Inhibition of hepatitis B viral replication in HepG2215 cells by siRNAs targeting hepatitis B virus X gene
Wang Li-jua
Abstract
Wang Li-jua
Abstract
Objective To observe the inhibition of hepatitis B viral replication in HepG2215 cells by siRNAs targeting hepatitis B virus X gene. Methods Four siRNAs against the X region of hepatitis B virus were chemically synthesized,and then were subjected to HepG2.2.15 cells by liposome-mediated transfection. The HBsAg and HbeAg in the supernatant were assayed by ELISA and HBV DNA by RT-PCR. Results At 30nmoL/L, the four siRNA had no obvious suppression in HBeAg and HbsAg expression (P0.05),while at the concentration of 60nmoL/L and 90nmoL/L,the inhibition of siRNA-1 and siRNA-4 were statistically significant with the inhibition rates of 41% and 43%;the HBV DNA replication was obviously reduced. Conclusion The chemically synthesized siRNAs can effectively inhibit hepatitis B viral replication in vitro.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To observe the inhibition of hepatitis B viral replication in HepG2215 cells by siRNAs targeting hepatitis B virus X gene. Methods Four siRNAs against the X region of hepatitis B virus were chemically synthesized,and then were subjected to HepG2.2.15 cells by liposome-mediated transfection. The HBsAg and HbeAg in the supernatant were assayed by ELISA and HBV DNA by RT-PCR. Results At 30nmoL/L, the four siRNA had no obvious suppression in HBeAg and HbsAg expression (P0.05),while at the concentration of 60nmoL/L and 90nmoL/L,the inhibition of siRNA-1 and siRNA-4 were statistically significant with the inhibition rates of 41% and 43%;the HBV DNA replication was obviously reduced. Conclusion The chemically synthesized siRNAs can effectively inhibit hepatitis B viral replication in vitro.
Key concepts: HBeAg, Virology, Small interfering RNA, HBsAg, Hepatitis B virus, Transfection, Viral replication, Hepatitis B virus PRE beta