Biliary carcinomas arising in patients who have undergone bilioenterostomy is a clinical concern. Thus, we investigated if bilioenterostomy influences biliary carcinogenesis in hamsters. Syrian hamsters were divided into three groups according to the operative procedure: simple laparotomy (SL), choledochoduodenostomy (CD), and choledochojejunostomy (CJ). The animals were given no chemical carcinogens during the experiments and five to six hamsters in each group were killed every 20 weeks for up to 120 weeks after surgery. There were 37, 32, and 38 hamsters in the SL, CD, and CJ groups, respectively. Cholangiocarcinomas developed in 5.4%, 15.6%, and 23.7% of hamsters in the SL group, the CD group, and the CJ group, respectively. The incidence of biliary carcinoma was significantly higher in the bilioenterostomy groups, especially the CJ group (P < 0.05), than in the SL group. Tumor latency periods after surgery were 20 to 40 weeks shorter in the bilioenterostomy groups than in the SL group. Persistent cholangitis and bile stasis were observed in the bilioenterostomy groups, and there was a significant correlation between cholangitis and biliary carcinogenesis in the CD group. The proliferative cell nuclear antigen (PCNA) labeling index of the biliary epithelium was elevated in the bilioenterostomy groups. Thus, we conclude that persistent cholangitis after bilioenterostomy accelerates biliary carcinogenesis by activating the biliary epithelial cell kinetics.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Coyle KA, Bradley EL, III. Cholangiocarcinoma developing after simple excision of a type II choledochal cyst. South Med. J. 1992 85:540–544.
Watanabe Y, Toki A, Todani T. Bile duct cancer developed after cyst excision for choledochal cyst. J. Hepatobiliary Pancreat. Surg. 1999 6:207–212.
Strong RW. Late bile duct cancer complicating biliary-enteric anastomosis for benign disease. Am. J. Surg. 1999 177:472–474.
Tocchi A, Mazzoni G, Liotta G, Lepre L, Cassini D, Miccini M. Late development of bile duct cancer in patients who had biliary-enteric drainage for benign disease: a follow-up study of more than 1,000 patients. Ann. Surg. 2001 234:210–214.
Hakamada K, Sasaki M, Endoh M, Itoh T, Morita T, Konn M. Late development of bile duct cancer after sphincteroplasty: a ten- to twenty-two-year follow-up study. Surgery 1997 121, 488–492.
Tanaka M, Takahata S, Konomi H, Matsunaga H, Yokohata K, Takeda T, Utsunomia N, Ikeda S. Long-term consequence of endoscopic sphincterotomy for bile duct stones. Gastrointest. Endosc. 1998 48:465–469.
Tajima Y, Eto T, Tsunoda T, Tomioka T, Inoue K, Fukahori T, Kanematsu T. Induction of extrahepatic biliary carcinoma by N-nitrosobis(2-oxopropyl)amine in hamsters given chole-cystoduodenostomy with dissection of the common duct. Jpn. J. Cancer Res. 1994 85:780–788.
Ikematsu Y, Tomioka T, Tajima Y, Tsunoda T, Kanematsu T. Cholecystokinin promotes biliary carcinogenesis in hamster model. World J. Surg. 1995 19:847–851.
Ogura Y, Matsuda S, Usui M, Hanamura N, Kawarada Y. Effect of pancreatic juice reflux into biliary tract on N-nitrosobis(2-oxopropyl)amine (BOP)-induced biliary carcinogenesis in Syrian hamsters. Dig. Dis. Sci. 1999 44:79–86.
Takahashi M, Pour P, Althoff J, Donnelly T. The pancreas of the Syrian hamster (Mesocricetus auratus). Lab. Anim. Sci. 1977 27:336–342.
Singhal AK, Sadowsky JF, McSherry CK, Mosbach E.H. Effect of cholesterol and bile acids on the regulation of cholesterol mechanism in hamster. Biochim. Biophys. Acta 1983 752:214–222.
Rinderknecht H, Maset R, Collias K, Carmack C. Pancreatic secretory profiles of protein, digestive, and lysosomal enzymes in Syrian golden hamster. Effect of secretin and chole-cystokinin. Dig. Dis. Sci. 1983 28:518–525.
Lee S, Chalters AC, Chandler JG, Orloff MJ. A technique for orthotopic liver transplantation in the rat. Transplantation 1973 16:664–669.
Kitajima T, Tajima Y, Onizuka S, Matsuzaki S, Matsuo K, Kanemastu T. Linkage of persistent cholangitis after bilioenterostomy with biliary carcinogenesis in hamsters. J. Exp. Clin. Cancer Res. 2000 19:453–458.
Turusov V, Mohr U (Eds.). Pathology of tumors in laboratory animals: tumours of the liver. Volume III—tumors of the hamster. (1996) International Agency for Research on Cancer, Lyon, 79–108.
Pour P, Mohr U, Cardesa A, Althoff J, Kmoch N. Spontaneous tumors and common diseases in two colonies of Syrian hamsters. II. Respiratory tract and digestive system. J. Natl. Cancer Inst. 1977 56:937–948.
Ikematsu Y, Tomioka T, Yamanaka S, Tajima Y, Tsunoda T, Kanematsu T. Bilioenterostomy enhances biliary carcinogenesis in hamsters. Carcinogenesis 1996 17:1505–1509.
Ohta T, Nagakawa T, Ueda N, Nakamura T, Akiyama T, Ueno K, Miyazaki I. Mucosal dys-plasia of the liver and the intraductal variant of peripheral cholangiocarcinoma in hepatolithi-asis. Cancer 1999 68:2217–2223.
Sheen-Chen SM, Chou FF, Eng HL. Intrahepatic cholangiocarcinoma in hepatolithiasis: a frequently overlooked disease. J. Surg. Oncol. 1991 47:131–135.
Falchuk KR, Lesser PB, Galdabini JJ, Isselbacher KJ. Cholangiocarcinoma as related to chronic intrahepatic cholangitis and hepatolithiasis. Case report and review of the literature. Am. J. Gastroenterol. 1976 66:57–61.
Chijiiwa K, Ichimiya H, Kuroki S, Koga A, Nakamura F. Late development of cholangiocar-cinoma after the treatment of hepatolithiasis. Surg. Gynecol. Obstet. 1993 177:279–282.
Miyachi K, Fritzler MJ, Ten EM. Autoantibodies to a nuclear antigen in proliferating cells. J. Immunol. 1978 121:2228–2234.
Hall PA, Levinson DA, Woods AL. Proliferating cell nuclear antigen (PCNA) immunolocali-zation in paraffin sections: an index of cell proliferation with evidence of deregulated expression in some neoplasms. J. Pathol. 1990 162:285–294.
Soon Lee C. Difference in cell proliferation and prognostic significance of proliferating cell nuclear antigen and Ki-67 antigen immunoreactivity in in situ and invasive carcinoma of the extrahepatic biliary tract. Cancer 1996 78:1881–1887.
Nishida T, Nakao K, Hamaji M, Nakahara M, Tsujimoto M. Prognostic significance of pro-liferative cell nuclear antigen in carcinoma of the extrahepatic bile duct. World J. Surg. 1997 21:634–639.
Fujii H, Yang Y, Tang R, Kunimoto K, Itakura J, Mogaki M, Matsuda M, Suda K, Nobukawa B, Matsumoto Y. Epithelial cell proliferation activity of the biliary ductal system with congenital biliary malformations. J. Hepatobiliary Pancreat. Surg. 1999 6:294–302.
Jung YS, Lee KJ, Kim H, Kim WH, Kim IG, Yoo BM, Kim JH, Kim MW. Risk factor for extrahepatic bile duct cancer in patients with anomalous pancreaticobiliary duct union. Hepatogastroenterology 2004 51:946–949.
Kitajima T, Tajima Y, Matsuzaki S, Kuroki T, Fukuda K, Kanematsu T. Acceleration of spontaneous biliary carcinogenesis in hamsters by bilioenterostomy. Carcinogenesis 2003 24:133–137.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2009 Springer
About this chapter
Cite this chapter
Kitajima, T., Matsuzaki, S., Kuroki, T., Fukuda, K., Tajima, Y., Kanematsu, T. (2009). Spontaneous Biliary Carcinogenesis. In: Tajima, Y., Kuroki, T., Kanematsu, T. (eds) Hepatobiliary and Pancreatic Carcinogenesis in the Hamster. Springer, Tokyo. https://doi.org/10.1007/978-4-431-87773-8_8
Download citation
DOI: https://doi.org/10.1007/978-4-431-87773-8_8
Publisher Name: Springer, Tokyo
Print ISBN: 978-4-431-87772-1
Online ISBN: 978-4-431-87773-8
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)