Correlation between Expression Differences of Epithelial-Mesenchymal Transition (EMT) in Cholangiocarcinoma Tissue
- 1 The Fourth People’s Hospital of Haikou, Haikou, China
- 2 The Fourth People’s Hospital of Haikou, Haikou, China
- 3 The Fourth People’s Hospital of Haikou, Haikou, China
- 4 Hainan General Hospital, Haikou, China
Abstract
Background: By studying the expression of epithelial-mesenchymal transition regulators in cholangiocarcinoma and intrahepatic duct stones, the correlation between the expression of epithelial-mesenchymal transition regulators and cholangiocarcinoma was revealed. Objective: The objective is to investigate the correlation between the expression of epithelial-mesenchymal transition (EC) regulatory factors and cholangiocarcinoma in patients with intrahepatic duct stones and cholangiocarcinoma, to investigate the relationship between clinicopathological features and prognosis, and to observe the expression of molecular markers of epithelial-mesenchymal transition (EMT) in intrahepatic duct stones and bile duct carcinoma. Methods: Twenty cases of primary cholangiocarcinoma, 20 cases of intrahepatic cholangiolithiasis complicated with cholangiocarcinoma, and 20 cases of intrahepatic cholangiolithiasis specimens were collected from the Fourth People’s Hospital and the friendly medical unit of Haikou. Immunohistochemistry was used to detect the expression differences of EMT-related molecular markers Twisit1, Twisit2, E-cadherin, N-cadherin, and Vimentin in paraffin sections of normal intrahepatic bile duct tissues and patients with intrahepatic duct stones and cholangiocarcinoma. Results: Immunohistochemical staining revealed epithelial-mesenchymal transition (EMT) in intrahepatic cholangiocarcinoma tissue, intrahepatic cholangiolithiasis with cholangiocarcinoma, intrahepatic cholangiolithiasis with normal intrahepatic cholangiolithiasis, such as Sit1, Twisit2, E-cadherin, N-cadherin, and Vimentin proteins were different. The expression of E-cadherin was decreased in cholangiocarcinoma tissue and intrahepatic cholangiolithiocarcinoma combined with cholangiocarcinoma (P < 0.05), while the expression of N-cadherin and Vimentin was up-regulated (P < 0.05). The expression of Twisit1 and Twisit2 had no difference (P > 0.05). There was no difference in the expression of intrahepatic bile duct stones and EMT (P > 0.05). Conclusion: The expression of E-cadherin, the molecular marker of EMT, was down-regulated, while the expression of N-cadherin and Vimentin was up-regulated. Age, gender, depth of tumor invasion, degree of tumor differentiation and lymph node metastasis were correlated with the expression of EMT in intrahepatic cholangiocarcinoma.
- Jemal, A., Bray, F., Center, M.M., et al. (2011) Global Cancer Statistics. CA: A Cancer Journal for Clinicians, 61, 69-90. https://doi.org/10.3322/caac.20107
- Halme, L., Arola, J., Numminen, K., et al. (2012) Biliary Dysplasia in Patients with Primary Sclerosing Cholangitis:additional Value of DNA Ploidity. Liver International, 32, 783-789. https://doi.org/10.1111/j.1478-3231.2011.02672.x
- Guglielmi, A., Ruzzenente, A., et al. (2014) Hepatolithiasis-Associated Cholangiocarcinoma:Results from a Multi-Institutional National Database on a Case Series of 23 Patients. European Journal of Surgical Oncology, 40, 567-575. https://doi.org/10.1016/j.ejso.2013.12.006
- Jusakul, A., Kongpetch, S. and Teh, B.T. (2015) Genetics of Opisthorchis Viverrini-Related Cholangiocarcinoma. Current Opinion in Gastroenterology, 31, 258-263. https://doi.org/10.1097/MOG.0000000000000162
- Lee, B.S., Park, E.C., Park, S.W., et al. (2015) Hepatitis B Virus Infection, Diabetes Mellitus, and Their Synergism for Cholangiocarcinoma Development: A Case-Control Study in Korea. World Journal of Gastroenterology, 21, 502-510. https://doi.org/10.3748/wjg.v21.i2.502
- Shaib, Y.H., El-Serag, H.B., Davila, J.A., et al. (2005) Risk Factors of Intrahepatic Cholangiocarcinoma in the United States: A Case-Control Study. Gastroenterology, 128, 620-626. https://doi.org/10.1053/j.gastro.2004.12.048
- Fujita, T. (2013) Analyzing Risk Factors for Intrahepatic Cholangiocarcinoma. Hepatology, 58, 1862-1863. https://doi.org/10.1002/hep.26448
- Okuda, K., Nakanuma, Y. and Miyazaki, M. (2002) Cholangiocarcinoma: Recent Progress. Part 1: Epidemiology and Etiology. Journal of Gastroenterology and Hepatology, 17, 1049-1055. https://doi.org/10.1046/j.1440-1746.2002.02781.x
- Valastyan, S. and Weinberg, R.A. (2011) Tumor metastasis: Molecular Insights and Evolving Paradigms. Cell, 147, 275-292. https://doi.org/10.1016/j.cell.2011.09.024
- Kim, D., Xing, T., Yang, Z., et al. (2017) Epithelial Mesenchymal Transition in Embryonic Development, Tissue Repair and Cancer: A Comprehensive Overview. Journal of Clinical Medicine, 7, 25 p. https://doi.org/10.3390/jcm7010001
- Thiery, J.P. and Lim, C.T. (2013) Tumor Dissemination: An EMT Affair. Cancer Cell, 23, 272-273. https://doi.org/10.1016/j.ccr.2013.03.004
- Clark, A.G. and Vignjevic, D.M. (2015) Modes of Cancer Cell Invasion and the Role of the Microenvironment. Current Opinion in Cell Biology, 36, 13-22. https://doi.org/10.1016/j.ceb.2015.06.004