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The
correlation between the malignant proliferation on
cholangiocarcinoma cell lines and in bile from
Helicobacter pylori infected patients with biliary tract
stones
Xudong Xu1, Quan Sun2,
Zhisu Liu2, Lin Zhang1, Zhiyong Luo1,
Yun Xia1 and Yaqun Wu1*
1Department of General
Surgery, Tongji Hospital, Tongji Medical College, Huazhong
University of Science and Technology, Wuhan 430030, P.R.
China
2Department
of General Surgery, Zhongnan Hospital, Wuhan University,
Wuhan 430071, P.R. China.
*Corresponding author, E-mail:
wyqmd@126.com. Tel: 86-27-83663819. Fax:
+86-27-83646605.
Accepted 25 May, 2010 |
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Helicobacter pylori
has been detected in human tissue and is a candidate for
etiologic investigations on the causes of hepatic and
biliary tract diseases, but reliable serologic tests need to
be developed in order to pursue such investigations. The aim
of this study was to assess the correlation between the
infection of H. pylori in bile from patients with
biliary tract stones and the proliferation of human
cholangiocarcinoma and its mechanism. Choledocholithiasis
bile with positive H. pylori (PCB),
Choledocholithiasis bile with negative H. pylori
(NCB) and normal bile (NB) were part of the
study. Cholangiocarcinoma cell lines QBC939 and TFK-1 were
analyzed. The proliferative effects were measured by
methabenzthiazuron (MTT) assay. Cell cycle and apoptosis
were analyzed by flow cytometry. Compared with NB and NCB,
PCB significantly promoted the proliferation of
cholangiocarcinoma cell lines QBC939 and TFK-1. The
proliferative index in PCB group was obviously higher than
that in NCB group after being treated with 1% PCB for 48 h
(p
<
0.05). As far as the apoptosis rate was concerned, there
were no obvious differences between PCB group and NCB group
(p
<
0.05), same as between PCB group and NB group (p
< 0.05). The percentage of S phase
increased remarkably in PCB group compared with NCB group,
while the percentage of G0/G1 phase
decreased remarkably in PCB group compared with NCB group.
It was suggested that PCB can greatly promote the malignant
proliferation of human cholangiocarcinoma cell lines QBC939
and TFK-1, and the mechanism was affected by the changes of
cell cycle. So we can predict that there was perhaps a close
relation between H. pylori infection and
cholangiocarcinoma.
Key words:
Malignant proliferation, Helicobacter pylori,
cholelithiasis, bile, cholangiocarcinoma. |