Metallothionein and apoptosis in primary human hepatocellular carcinoma (HCC) from Northern China

Citation
L. Cai et al., Metallothionein and apoptosis in primary human hepatocellular carcinoma (HCC) from Northern China, ANTICANC R, 18(6B), 1998, pp. 4667-4672
Citations number
33
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
18
Issue
6B
Year of publication
1998
Pages
4667 - 4672
Database
ISI
SICI code
0250-7005(199811/12)18:6B<4667:MAAIPH>2.0.ZU;2-H
Abstract
Background: Metallothionein (MT), acting as an antioxidant and zinc binding protein, may plan an important role in regulation of apoptosis. Its differ ential expression has been documented in various human tumours. Materials a nd Methods: MT expression by immunohistochemical staining with a polyclonal antibody and apoptotic cells (APC) by TUNEL technique were investigated in 20 cases of hepatocellular carcinoma (HCC) and 2 normal livers from Northe rn China. Adjacent normal liver was available from 9 of these cases and 6 h ad adjacent cirrhotic tissue. There was no difference for MT staining and i ncidence of APC between normal liver and adjacent normal liver, and thus bo th were used as control liver. Results: Control liver had consistent MT sta ining with very low incidence of APC. Adjacent cirrhotic liver showed the s ame intensity of MT staining, with a similar incidence of APC to control li ver. Twelve of 20 HCC cases (60%) showed no MT staining, and the rest also showed a low grade of MT staining as compared with control or adjacent cirr hotic livers. The incidence of APC in HCC was markedly higher than that in control liver or adjacent cirrhotic liver. The negative correlation of numb ers of APC with MT expression was statistically significant (p < 0.005). Th e high incidence of APC in liver with a low MT expression was confirmed in double staining for MT and APC. Conclusions: The present investigation from Northern Chinese samples has shown that MT expression in HCC was different from that in other human tumours, such as breast carcinoma. This suggests a different pattern of expression of MT protein in these two kinds of cance r. This investigation is important in understanding the mechanisms of the d rug resistance of tumour cells, and may help to design better treatment str ategies.