Abstract: ［Abstract］Objective　To observe overexpressional effects of FHIT gene on proliferation， apoptosis， invasion and cell cycle of human hepatocellular carcinoma cells including HepG2，Hep3B and Huh7. Method　The pLVX-IRES-FHIT slow virus recombinant vector was constructed and transfected into HepG2， Hep3B and Huh7 cells. We detected the infection of cell proliferation， apotosis， invasion and cell cycle of these cells with overexpression of FHIT and analyzed the relationship of biological effects and time gradient by MTT，Annexin V/PI using cell cycle detection technology and Transwell experiment. Results　According to DNA sequencing，the pLVX-IRES-FHIT slow virus recombinant vector was constructed successfully. （1）MTT tests showed that proliferation activity of HepG2，Hep3B and Huh7 with pLVX-IRES-FHIT transfection was reduced significantly in 48 hours and the inhibition was stable after 72 hours. The inhabitation in the control group was not significant（P＜0.05）. AnnexinV/PI double staining method showed that no significant difference of apoptosis level was seen after 48h among three hepatoma cells（P＞0.05）. The order of inhibitional proliferation activity from high to low was HepG2， Hep3B and Huh7；（2） Transwell tests showed that invasive activity of HepG2， Hep3B and Huh7 with pLVX-IRES-FHIT transfection was inhibited （P＜0.05）. The control group was not sinificantly inhibited （P＜0.05）. The order of invasive activity was HepG2＞Hep3B＞Huh7；（3） Cell cycle test showed that the number of cells in G0/G1 stage increased whereas decreased in stage S. Hep3B and Huh7 cells in the control group were not significantly inhibited （P＞0.05）. The influence of FHIT over expression to these cells was that cell cycle stopped in S stage， and sequence of cell number in G0/G1 was HepG2＜Hep3B＜Huh7．Conclusion　A positive correlation was found between FHIT expression and cellular differentiation on hepatoma cells. FHIT gene may be a potential gene therapy for human hepatocellular carcinoma.