Reduced expression of P120 catenin in cholangiocarcinoma correlated with tumor clinicopathologic parameters
AIM: To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC). METHODS: An immunohistochemical study of E-cadherin and P120 catenin was performed on 42 specimens of ICC with a Dako Envision kit. RESULTS: The expressi...
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Published in | World journal of gastroenterology : WJG Vol. 14; no. 23; pp. 3739 - 3744 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Department of Ultrasonic Intervention, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China%International Cooperation Laboratory on Signal Transduction, Eastern Hepatobilliary Surgery Institute, Second Military Medical University, Shanghai 200438, China
21.06.2008
The WJG Press and Baishideng |
Subjects | |
Online Access | Get full text |
ISSN | 1007-9327 2219-2840 |
DOI | 10.3748/wjg.14.3739 |
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Abstract | AIM: To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC).
METHODS: An immunohistochemical study of E-cadherin and P120 catenin was performed on 42 specimens of ICC with a Dako Envision kit.
RESULTS: The expression of E-cadherin and P120 was reduced in 27 cases (64.3%) and 31 cases (73.8%), respectively. Both E-cadherin and P120 expressions were significantly correlated with the tumor histological grade (χ^2 = 9.333, P = 009 and χ^= 11.71, P = 0.003), TNM stage (χ^= 8.627, P = 0.035 and χ^= 13.123, P = 0.004), intrahepatic metastasis (χ^= 7.292, P = 0.007 and χ^= 4.657, P = 0.041, respectively) and patients′ survival (χ^= 6.351, P = 0.002 and χ^= 4.023, P = 0.000, respectively). In addition, the expression of P120 was in concordance with that of E-cadherin (χ^ = 13.797, P = 0.000), indicating that the expression of P120 may be dependent on that of E-cadherin. Finally, only P120 expression was found to be an independent prognostic factor in Cox regression model (r = 0.088, P = 0.049).
CONCLUSION: Down-regulated expression of E-cadherin and P120 occurs frequently in ICC and contributes to the progression and development of tumor. Both of them may be valuable biologic markers for predicting tumor invasion, metastasis and patients′ survival, but only P120 is an independent prognostic factor for ICC. |
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AbstractList | R73; AIM: To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC).METHODS: An immunohistochemical study of E-cadherin and P120 catenin was performed on 42 specimens of ICC with a Dako Envision kit.RESULTS: The expression of E-cadherin and P120 was reduced in 27 cases (64.3%) and 31 cases (73.8%), respectively. Both E-cadherin and P120 expressions were significantly correlated with the tumor histological grade (X2=9.333, P=009 and X2=11.71, P=0.003), TNM stage (X2=8.627, P=0.035 and X2=13.123, P=0.004), intrahepatic metastasis (X2=7.292, P=0.007 and X2=4.657, P=0.041, respectively) and patients' survival (X2=6.351, P=0.002 and X2=4.023, P=0.000, respectively). In addition, the expression of P120 was in concordance with that of E-cadherin (X2=13.797, P=0.000), indicating that the expression of P120 may be dependent on that of E-cadherin. Finally, only P120 expression was found to be an independent prognostic factor in Cox regression model (r=0.088, P=0.049).CONCLUSION: Down-regulated expression of E-cadherin and P120 occurs frequently in ICC and contributes to the progression and development of tumor. Both of them may be valuable biologic markers for predicting tumor invasion, metastasis and patients' survival, but only P120 is an independent prognostic factor for ICC. AIM: To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC). METHODS: An immunohistochemical study of E-cadherin and P120 catenin was performed on 42 specimens of ICC with a Dako Envision kit. RESULTS: The expression of E-cadherin and P120 was reduced in 27 cases (64.3%) and 31 cases (73.8%), respectively. Both E-cadherin and P120 expressions were significantly correlated with the tumor histological grade (χ^2 = 9.333, P = 009 and χ^= 11.71, P = 0.003), TNM stage (χ^= 8.627, P = 0.035 and χ^= 13.123, P = 0.004), intrahepatic metastasis (χ^= 7.292, P = 0.007 and χ^= 4.657, P = 0.041, respectively) and patients′ survival (χ^= 6.351, P = 0.002 and χ^= 4.023, P = 0.000, respectively). In addition, the expression of P120 was in concordance with that of E-cadherin (χ^ = 13.797, P = 0.000), indicating that the expression of P120 may be dependent on that of E-cadherin. Finally, only P120 expression was found to be an independent prognostic factor in Cox regression model (r = 0.088, P = 0.049). CONCLUSION: Down-regulated expression of E-cadherin and P120 occurs frequently in ICC and contributes to the progression and development of tumor. Both of them may be valuable biologic markers for predicting tumor invasion, metastasis and patients′ survival, but only P120 is an independent prognostic factor for ICC. To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC).AIMTo investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC).An immunohistochemical study of E-cadherin and P120 catenin was performed on 42 specimens of ICC with a Dako Envision kit.METHODSAn immunohistochemical study of E-cadherin and P120 catenin was performed on 42 specimens of ICC with a Dako Envision kit.The expression of E-cadherin and P120 was reduced in 27 cases (64.3%) and 31 cases (73.8%), respectively. Both E-cadherin and P120 expressions were significantly correlated with the tumor histological grade (chi2 = 9.333, P = 009 and chi2 = 11.71, P = 0.003), TNM stage (chi2= 8.627, P = 0.035 and chi2 = 13.123, P = 0.004), intrahepatic metastasis (chi2= 7.292, P = 0.007 and chi2 = 4.657, P = 0.041, respectively) and patients' survival (chi2= 6.351, P = 0.002 and chi2 = 4.023, P = 0.000, respectively). In addition, the expression of P120 was in concordance with that of E-cadherin (chi2 = 13.797, P = 0.000), indicating that the expression of P120 may be dependent on that of E-cadherin. Finally, only P120 expression was found to be an independent prognostic factor in Cox regression model (r = 0.088, P = 0.049).RESULTSThe expression of E-cadherin and P120 was reduced in 27 cases (64.3%) and 31 cases (73.8%), respectively. Both E-cadherin and P120 expressions were significantly correlated with the tumor histological grade (chi2 = 9.333, P = 009 and chi2 = 11.71, P = 0.003), TNM stage (chi2= 8.627, P = 0.035 and chi2 = 13.123, P = 0.004), intrahepatic metastasis (chi2= 7.292, P = 0.007 and chi2 = 4.657, P = 0.041, respectively) and patients' survival (chi2= 6.351, P = 0.002 and chi2 = 4.023, P = 0.000, respectively). In addition, the expression of P120 was in concordance with that of E-cadherin (chi2 = 13.797, P = 0.000), indicating that the expression of P120 may be dependent on that of E-cadherin. Finally, only P120 expression was found to be an independent prognostic factor in Cox regression model (r = 0.088, P = 0.049).Down-regulated expression of E-cadherin and P120 occurs frequently in ICC and contributes to the progression and development of tumor. Both of them may be valuable biologic markers for predicting tumor invasion, metastasis and patients' survival, but only P120 is an independent prognostic factor for ICC.CONCLUSIONDown-regulated expression of E-cadherin and P120 occurs frequently in ICC and contributes to the progression and development of tumor. Both of them may be valuable biologic markers for predicting tumor invasion, metastasis and patients' survival, but only P120 is an independent prognostic factor for ICC. To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC). An immunohistochemical study of E-cadherin and P120 catenin was performed on 42 specimens of ICC with a Dako Envision kit. The expression of E-cadherin and P120 was reduced in 27 cases (64.3%) and 31 cases (73.8%), respectively. Both E-cadherin and P120 expressions were significantly correlated with the tumor histological grade (chi2 = 9.333, P = 009 and chi2 = 11.71, P = 0.003), TNM stage (chi2= 8.627, P = 0.035 and chi2 = 13.123, P = 0.004), intrahepatic metastasis (chi2= 7.292, P = 0.007 and chi2 = 4.657, P = 0.041, respectively) and patients' survival (chi2= 6.351, P = 0.002 and chi2 = 4.023, P = 0.000, respectively). In addition, the expression of P120 was in concordance with that of E-cadherin (chi2 = 13.797, P = 0.000), indicating that the expression of P120 may be dependent on that of E-cadherin. Finally, only P120 expression was found to be an independent prognostic factor in Cox regression model (r = 0.088, P = 0.049). Down-regulated expression of E-cadherin and P120 occurs frequently in ICC and contributes to the progression and development of tumor. Both of them may be valuable biologic markers for predicting tumor invasion, metastasis and patients' survival, but only P120 is an independent prognostic factor for ICC. AIM: To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC). METHODS: An immunohistochemical study of E-cadherin and P120 catenin was performed on 42 specimens of ICC with a Dako Envision kit. RESULTS: The expression of E-cadherin and P120 was reduced in 27 cases (64.3%) and 31 cases (73.8%), respectively. Both E-cadherin and P120 expressions were significantly correlated with the tumor histological grade (χ 2 = 9.333, P = 009 and χ 2 = 11.71, P = 0.003), TNM stage (χ 2 = 8.627, P = 0.035 and χ 2 = 13.123, P = 0.004), intrahepatic metastasis (χ 2 = 7.292, P = 0.007 and χ 2 = 4.657, P = 0.041, respectively) and patients’ survival (χ 2 = 6.351, P = 0.002 and χ 2 = 4.023, P = 0.000, respectively). In addition, the expression of P120 was in concordance with that of E-cadherin (χ 2 = 13.797, P = 0.000), indicating that the expression of P120 may be dependent on that of E-cadherin. Finally, only P120 expression was found to be an independent prognostic factor in Cox regression model ( r = 0.088, P = 0.049). CONCLUSION: Down-regulated expression of E-cadherin and P120 occurs frequently in ICC and contributes to the progression and development of tumor. Both of them may be valuable biologic markers for predicting tumor invasion, metastasis and patients’ survival, but only P120 is an independent prognostic factor for ICC. |
Author | Bo Zhai He-Xin Yan Shu-Qin Liu Lei Chen Meng-Chao Wu Hong-Yang Wang |
AuthorAffiliation | Department of Ultrasonic Intervention, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200438, China International Cooperation Laboratory on Signal Transduction, Eastern Hepatobilliary Surgery Institute, Second Military Medical University, Shanghai 200438, China |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18595142$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1007/978-3-662-03432-3 10.1007/s00428-006-0291-5 10.1016/j.bbamcr.2006.07.005 10.1016/S1084-9521(04)00089-8 10.1002/hep.510240627 10.1016/j.jdermsci.2003.12.001 10.1002/hep.510270412 10.1046/j.1365-2559.2002.01392.x 10.1083/jcb.200605022 10.1002/jso.20344 10.1038/modpathol.3880409 10.1136/jcp.2005.026575 10.1046/j.1432-0436.2002.700911.x 10.1006/mcbr.1999.0155 10.1200/JCO.2002.08.159 10.1053/jhep.2001.25087 10.1038/modpathol.3800965 10.3892/ijo.27.4.973 10.1242/jcs.00724 10.1158/0008-5472.CAN-05-1947 10.1046/j.0106-9543.2001.01580.x 10.1046/j.0956-5507.2003.00090.x 10.1038/sj.onc.1207439 10.1053/gast.2003.50142 |
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Keywords | Clinicopathologic feature P120 Survival Invasion and metastasis Intrahepatic cholangiocarcinoma |
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Notes | P120; Intrahepatic cholangiocarcinoma; Clinicopathologic feature; Invasion and metastasis; Survival Clinicopathologic feature 14-1219/R Intrahepatic cholangiocarcinoma P120 R735.7 Survival Invasion and metastasis ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Fax: +86-21-65566851 Telephone: +86-21-25070846 Correspondence to: Hong-Yang Wang, International Cooperation Laboratory on Signal Transduction, Eastern Hepatobilliary Surgery Institute, Second Military Medical University, Shanghai 200438, China. hywangk@online.sh.cn Author contributions: Zhai B wrote the paper and organized the figures and patient data, Yan HX and Liu SQ did the immunohistochemical staining assays; Chen L carried out the statistical analysis; Wu MC and Wang HY helped write, organize, and correct the paper; Wang HY supervised the writing and organization process. |
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Snippet | AIM: To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC).
METHODS: An... To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC). An... To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC).AIMTo investigate... R73; AIM: To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC).METHODS:... AIM: To investigate the relationship between the expression of P120 and the clinicopathologic parameters in intrahepatic cholangiocarcinoma (ICC). METHODS: An... |
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SubjectTerms | Adult Aged Bile Duct Neoplasms - chemistry Bile Duct Neoplasms - mortality Bile Duct Neoplasms - pathology Bile Ducts, Intrahepatic - chemistry Bile Ducts, Intrahepatic - pathology Biomarkers, Tumor - analysis Cadherins - analysis Catenins Cell Adhesion Molecules - analysis Cholangiocarcinoma - chemistry Cholangiocarcinoma - mortality Cholangiocarcinoma - pathology Down-Regulation Female Humans Immunohistochemistry Kaplan-Meier Estimate Male Middle Aged Neoplasm Metastasis Neoplasm Staging P120 Phosphoproteins - analysis Prognosis Proportional Hazards Models Rapid Communication 临床特征 肝肿瘤 |
Title | Reduced expression of P120 catenin in cholangiocarcinoma correlated with tumor clinicopathologic parameters |
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