Protective effects of Lycopene on hepatocarcinogenesis in Long-Evans Cinnamon rats

A high incidence of hepatocellular carcinoma in long surviving long Evans Cinnamon (LEC) ratswas reported. In order to investigate whether Lycopene and Sho-saiko-to (TJ-9) haveanti - hepatocarcinogenesis,Lycopene和TJ-9 administered orally for one and a half years in LEC rats and studied theeffect to natural hepatocarcinogenesis of these rats.所有rats都在76周内生活autopsy and histopathological examination was performed. Fifty five percent (11 /20) of control ratshad HCC, 55% (11/20) of Lycopene group had HCC, and，75% (12/16) of TJ-9 group had HCC in 76 week life. Percentage of HCC bearing rats did not differamong the three groups. Number of preneoplastic lesions stained with GST-P per lcm . Number of preneoplastic lesionsliver specimen was smaller in Lycopene group compared with control group (p = 0.00124) .Concentration of iron ion in the liver of Lycopene group lower compared with TJ-9 group（p=0.0207）. Concerning the报告that iron deprivation also inhibited the liver tumor development，the finding of lower concentration of iron ion in the liver of Lycopene group compared with TJ-9group has a possibility to some link to the result of lower number of preneoplastic lesionsstained with GST-P. Serum α-fetoprotein levels were 331.0±249.1 ng/ml in control groups (n=9)，and 559.4±1211.4 ng/ml in Lycopene group (n=11)，and 5883±653.4 ng/ml in TJ-9 group (n=11). There were no differences in serum α-fetoprotein levelsamong the three groups. In conclusion，anti-hepatocarcinogenesis not foud in Lycopene and TJ-9. Further study will be needed toclarify the preventive effect of preneoplastic lesions by Lycopene。

A high incidence of hepatocellular carcinoma (HCC) in long surviving Long Evans Cinnamon (LEC) rats was reported. In order to investigate whether Lycopene and Sho-saiko-to (TJ-9) have anti-hepatocarcinogenesis, Lycopene and TJ-9 were administered orally for one and a half years in LEC rats and studied the effect to natural hepatocarcinogenesis of these rats. All rats were sacrificed in 76 week life for autopsy and histopathological examination was performed. Fifty five percent (1 1/20) of control rats had HCC, 55% (11/20) of Lycopene group had HCC, and, 75% (12/16) of TJ-9 group had HCC in 76 week life. Percentage of HCC bearing rats did not differ among the three groups. Number of preneoplastic lesions stained with GST-P per lcmィイD12ィエD1 of the liver specimen was smaller in Lycopene group compared with control group (p = 0.00124) . Concentration of iron ion in the liver of Lycopene group were lower compared with TJ-9 group (p=0.0207). Concerning the report that iron deprivation also inhibited the liver tumor development, the finding of lower concentration of iron ion in the liver of Lycopene group compared with TJ-9 group has a possibility to have some link to the result of lower number of preneoplastic lesions stained with GST-P. Serum α-fetoprotein levels were 331.0 ± 249.1 ng/ml in control groups (n=9), and 559.4 ± 1211.4 ng/ml in Lycopene group (n=11), and 5883 ± 653.4 ng/ml in TJ-9 group (n=11). There were no differences in serum α-fetoprotein levels among the three groups. In conclusion, anti-hepatocarcinogenesis were not foud in Lycopene and TJ-9. Further study will be needed to clarify the preventive effect of preneoplastic lesions by Lycopene.