TY - JOUR
T1 - Possible involvement of Enterococcus infection in the pathogenesis of chronic pancreatitis and cancer
AU - Maekawa, Tomohiro
AU - Fukaya, Risako
AU - Takamatsu, Shinji
AU - Itoyama, Saki
AU - Fukuoka, Tomoya
AU - Yamada, Makoto
AU - Hata, Tomoki
AU - Nagaoka, Satoshi
AU - Kawamoto, Koichi
AU - Eguchi, Hidetoshi
AU - Murata, Kohei
AU - Kumada, Takashi
AU - Ito, Toshifumi
AU - Tanemura, Masahiro
AU - Fujimoto, Kahoko
AU - Tomita, Yasuhiko
AU - Tobe, Toru
AU - Kamada, Yoshihiro
AU - Miyoshi, Eiji
N1 - Funding Information:
This study was supported by JSPS KAKENHI , Grant Number JP16H05226 , awarded to E. Miyoshi, and JP16K15428 , awarded to Y. Kamada. It was also supported, in part, by the Princess Takamatsu Cancer Research Fund awarded to E. Miyoshi.
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/12/2
Y1 - 2018/12/2
N2 - (Aim) Bacterial infection underlies the pathogenesis of many human diseases, including acute and chronic inflammation. Here, we investigated a possible role for bacterial infection in the progression of chronic pancreatitis. (Materials and Methods) Pancreatic juice was obtained from patients with pancreatic cancer (n = 20) or duodenal cancer/bile duct cancer (n = 16) and subjected to PCR using universal primers for the bacterial 16S ribosomal RNA gene. Bacterial species were identified by PCR using bile samples from four pancreatic cancer patients. PCR products were subcloned into T-vectors, and the sequences were then analyzed. Immunohistochemical and serologic analyses for Enterococcus faecalis infection were performed on a large cohort of healthy volunteers and patients with chronic pancreatitis or pancreatic cancer and on mice with caerulein-induced chronic pancreatitis. The effect of E. faecalis antigens on cytokine secretion by pancreatic cancer cells was also investigated. (Results) We found that 29 of 36 pancreatic juice samples were positive for bacterial DNA. Enterococcus and Enterobacter species were detected primarily in bile, which is thought to be a pathway for bacterial infection of the pancreas. Enterococcus faecalis was also detected in pancreatic tissue from chronic pancreatitis and pancreatic cancer patients; antibodies to E. faecalis capsular polysaccharide were elevated in serum from chronic pancreatitis patients. Enterococcus-specific antibodies and pancreatic tissue–associated E. faecalis were detected in mice with caerulein-induced chronic pancreatitis. Addition of Enterococcus lipoteichoic acid and heat-killed bacteria induced expression of pro-fibrotic cytokines by pancreatic cancer cells in vitro. (Conclusion) Infection with E. faecalis may be involved in chronic pancreatitis progression, ultimately leading to development of pancreatic cancer.
AB - (Aim) Bacterial infection underlies the pathogenesis of many human diseases, including acute and chronic inflammation. Here, we investigated a possible role for bacterial infection in the progression of chronic pancreatitis. (Materials and Methods) Pancreatic juice was obtained from patients with pancreatic cancer (n = 20) or duodenal cancer/bile duct cancer (n = 16) and subjected to PCR using universal primers for the bacterial 16S ribosomal RNA gene. Bacterial species were identified by PCR using bile samples from four pancreatic cancer patients. PCR products were subcloned into T-vectors, and the sequences were then analyzed. Immunohistochemical and serologic analyses for Enterococcus faecalis infection were performed on a large cohort of healthy volunteers and patients with chronic pancreatitis or pancreatic cancer and on mice with caerulein-induced chronic pancreatitis. The effect of E. faecalis antigens on cytokine secretion by pancreatic cancer cells was also investigated. (Results) We found that 29 of 36 pancreatic juice samples were positive for bacterial DNA. Enterococcus and Enterobacter species were detected primarily in bile, which is thought to be a pathway for bacterial infection of the pancreas. Enterococcus faecalis was also detected in pancreatic tissue from chronic pancreatitis and pancreatic cancer patients; antibodies to E. faecalis capsular polysaccharide were elevated in serum from chronic pancreatitis patients. Enterococcus-specific antibodies and pancreatic tissue–associated E. faecalis were detected in mice with caerulein-induced chronic pancreatitis. Addition of Enterococcus lipoteichoic acid and heat-killed bacteria induced expression of pro-fibrotic cytokines by pancreatic cancer cells in vitro. (Conclusion) Infection with E. faecalis may be involved in chronic pancreatitis progression, ultimately leading to development of pancreatic cancer.
UR - http://www.scopus.com/inward/record.url?scp=85055902585&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85055902585&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2018.10.169
DO - 10.1016/j.bbrc.2018.10.169
M3 - Article
C2 - 30401562
AN - SCOPUS:85055902585
SN - 0006-291X
VL - 506
SP - 962
EP - 969
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -