Objective：To construct the recombinant adenovirus（Rad） with expressing inhibitor 1 of differentiation（Id1），and to estab－lish its animal model. Methods：AdEasy-Id1，the recombinant adenovirus plasmid which had been constructed previously，was pack－aged in HEK293 cells to obtain recombinant adenovirus Id1（RAd-Id1）. Then the titer of virus was determined by green fluorescent protein（GFP） labeling method. The over-expression efficiency of Id1 was measured by qRT-PCR and Western blot in HepG2 cells infected with RAd-Id1，and the effect of Id1 on proliferation of HepG2 cells was detected by MTS assay. Animal model of Id1 expressing in liver tissue was established through the way of tail vein injection of RAd-Id1. In order to determine the suitable load of RAd-Id1 virus for infecting the mice，viral load gradient exper－iment was divided into PBS control group，RAd-GFP control group and RAd-Id1 experimental group（n=5/group）. Time gra－dient experiment examined once every 5 days as a group，a total of 7 group（n=5/group），to explore the appropriate time. The expression of Id1 as well as the changes of alpha fetal pro－tein（AFP） and carcinoembryonic antigen（CEA） in liver tissues were determined by Western blot. The level of Id1 antibody and the concentrations of AFP and CEA in serum were detected by ELISA. Results：Recombinant adenovirus plasmid containing Id1 gene was successfully established，then the corresponding adenovirus were acquired and the measured titer was 1.5×1011 GFU/mL. Western blot and qRT-PCR analysis showed that Id1 mRNA and protein levels significantly increased in HepG2 infected with RAd-Id1 for 48 h and 72 h respectively（P<0.01）. MTS assay reported that the values in RAd-Id1 group were higher than those in NC group and RAd-GFP group after 96 h（2.00±0.06 vs. 1.18±0.05，2.00±0.06 vs. 1.10±0.07；F=51.350，P=0.000）；Western blot results showed：when compared with PBS group and RAd-GFP group，the RAd-Id1 group’s levels of Id1 as well as AFP and CEA in liver was higher. ELISA results showed：the concentrations of AFP and CEA in serum were positively correlated with the load of RAd-Id1（rs AFP=0.903，PAFP=0.014；rs CEA=0.964，PCEA=0.002）. There was no significant difference among these concentrations of Id1 antibody in serum of mice infected with different load of RAd-Id1（P>0.05）. Conclusion：The RAd-Id1 is successfully constructed，which serves as the vector tool to study the effect of Id1 on hepatic neoplasm at the cellular level. Mouse animal model of RAd-Id1 accompanied with the elevation of both AFP and CEA in liver also has been successfully established by tail vein injection，which suggests that the ectopic expression of Id1 may be related to the expression of AFP and CEA，but further studies will be required to determine how the mecha－nism works.