The Effects of Transforming Growth Factor beta1 on Apoptosis in Rat Hepatocellular Carcinoma.
- Author:
Young Euy PARK
;
Young Hee CHOI
;
Won Yo LEE
;
Jin Ja PARK
;
Kyung Chan CHOI
;
Hyung Shik SHIN
- Publication Type:Original Article
- Keywords:
Rat;
Apoptosis;
TGF-beta1;
TGF-alpha;
Hepatocellular carcinoma
- MeSH:
Animals;
Apoptosis;
Carcinogenesis;
Carcinoma, Hepatocellular*;
Diethylnitrosamine;
DNA;
Doxorubicin;
Models, Animal;
Proliferating Cell Nuclear Antigen;
Rats*;
Rats, Sprague-Dawley;
S Phase;
Transforming Growth Factor alpha;
Transforming Growth Factor beta1*;
Transforming Growth Factors*
- From:Korean Journal of Pathology
1999;33(2):71-79
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Based upon the concept that carcinogenesis is associated with apoptosis, specific therapies designed to enhance the susceptibility of cancer cells to undergo apoptosis could be developed. Thus, in this paper, it was designed to investigate whether, using rat animal model with chemical-induced hepatocellular carcinoma, TGF-1 in vivo could induce apoptosis in cancer. The chemical hepatocarcinogenic procedure of Solt-Farber method was used on Sprague-Dawley rats. Experimental groups were divided into group A treated with the standard Solt-Farber regimen of diethylnitrosamine (DEN) and 2-Acetaminofluorene (AAF), group B TGF-, group C TGF-1, and group D adriamycin after hepatocellular carcinoma developed. For detection of apoptotic cells, apoptotic indices were examined by the in situ end DNA labelling method. The expression of proliferating cell nuclear antigen was examined by immunohistochemical staining. Apoptosis of rat hepatocellular carcinoma cells increased significantly to 4.92+/-2.32/HPF in the group C compared with the control group (A) (2.54+/-1.13/HPF; P<0.05). Two distinctly different populations of proliferating hepatocellular carcinoma cells were identified. The cells at G1/S boundary (weak granular staining) increased to 15.75+/-6.19/HPF and 6.45+/-2.93/HPF in the groups C and D, respectively, but decreased to 2.42+/-2.06/HPF in the group B compared with the control group (A) (6.38+/-2.18/HPF; p<0.05). The cells at S phase (strong granular staining) increased to 3.37+/-2.69/HPF in the group B but decreased to 0.32+/-0.47/HPF in the group D (p<0.05). In conclusion, these results indicate that the TGF-1 may be used as an effective anticancer agent.
