Possible correlation between iron deposition and enhanced proliferating activity in hepatitis C virus-positive hepatocellular carcinoma in Myanmar (Burma)
Possible correlation between iron deposition and enhanced proliferating activity in hepatitis C virus-positive hepatocellular carcinoma in Myanmar (Burma)
复制标题
缅甸丙型肝炎病毒阳性肝细胞癌中铁沉积与增殖活性增强之间可能存在相关性
DOI:
10.1007/s00535-006-1993-9
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发表时间:
2007
影响因子:
6.3
通讯作者:
T. Koji
中科院分区:
文献类型:
--
作者:
Kyaw Soe;Y. Hishikawa;Y. Fukuzawa;N. Win;Khine San Yin;K. Win;A. Myint;T. Koji
BackgroundThe aim of this study was to survey the effect of deposited iron on the cell kinetics of hepatitis C virus (HCV)-positive hepatocellular carcinoma (HCC) in Myanmar (Burmese) patients.MethodsFormalin-fixed and paraffin-embedded liver tissues from 34 Myanmar patients with HCC were used. To detect iron deposition, Prussian blue staining was performed. Cell proliferation and apoptosis were assessed by Ki-67 staining and by the terminal deoxynucleotidyl transferase (TdT)-mediated dUTP-biotin nick end labeling (TUNEL) assay, respectively. HCV RNA was detected by in situ hybridization, and HCV protein, Fas and Fas ligand (FasL) were localized by immunohistochemistry. To identify the subtype of lymphocytes, CD8 was used as a surface marker.ResultsIron deposition was found in 43% of the HCC cases, and was heavier in moderately differentiated HCC than in well-differentiated HCC. The Ki-67 labeling index (LI) in cancer cells was higher in Prussian blue-positive-HCC than in -negative HCC (3.8 ± 2.2 vs 1.5 ± 1.7, mean ± SD; P = 0.0067), whereas there was no significant difference between these groups in TUNEL LI. HCV protein was localized in cancer cells, and was found in 89% of the patients. In addition, Fas was expressed in HCC cells, and FasL was localized in HCC cells as well as in infiltrating CD8+ T lymphocytes. The frequency of apoptosis of HCC cells was correlated significantly with the population density of infiltrating CD8+ T lymphocytes.ConclusionsOur results indicated that, in Myanmar patients with HCC, iron deposition might accelerate hepatocarcinogenesis, by promoting cancer cell proliferation, without affecting the Fas/FasL apoptotic system.
影响因子:
4.8
作者:
Takehiko Koji;R. Brenner
通讯作者:
Takehiko Koji;R. Brenner
影响因子:
29.4
作者:
Kowdley, KV
通讯作者:
Kowdley, KV