The Value of Survivin Gene and Proliferation of Hepatocytes in Screening for Hepatocellular Carcinoma
Abstract
Methods: Total RNA was extracted from fresh specimens of HCC and liver cirrhosis. Survivin mRNA amplification was performed by reverse transcription polymerase chain reaction (RT-PCR). Immunostaining for PCNA was employed to assess liver cell proliferation activity in formalin-fixed, paraffin embedded liver specimens. Five liver specimens obtained from patients operated for hemangioma were used as normal control. The PCNA labeling index was determined as the mean value of positive cells in ten different microscopic fields.
Results: RT-PCR was performed in 17 HCC and 10 liver cirrhosis specimens, 11 HCC  specimens showed 344bps molecular survivin DNA band in 1% agarose  electrophoresis, but none of liver cirrhosis specimens showed positive  band. The survivin positive rate in HCC specimens was 64.7% (11/17); The  PCNA labeling index was 2.38 2.11 in 30 liver cirrhosis specimens,  while 10.08 12.28 in 30 HCC specimens, the latter was significantly  higher than the former, P = 0.003. The median PCNA labeling index of 11  survivin positive HCC specimens was 6.8 (from 0.5 to 40), which is  significantly higher than that of 6 survivin negative HCC specimens  (2.15). 
Conclusions: Survivin expressed in HCC  tissues but not in liver cirrhosis tissues, this phenomenon indicates  that the gene expression may occur at the late phase of liver cell  cancer transformation. Compared with survivin detection, the PCNA  detection on liver cells of cirrhosis patients is better to  differentiate high-risk HCC transformation among liver cirrhosis  patients.
Gastroenterol Res. 2009;2(6):333-337
doi: https://doi.org/10.4021/gr2009.12.1326


