Increased expression of EphA2 and E-N cadherin switch in primary hepatocellular carcinoma. Issue 6 (November 2013)
- Record Type:
- Journal Article
- Title:
- Increased expression of EphA2 and E-N cadherin switch in primary hepatocellular carcinoma. Issue 6 (November 2013)
- Main Title:
- Increased expression of EphA2 and E-N cadherin switch in primary hepatocellular carcinoma
- Authors:
- Fan, Min
Liu, Yu
Xia, Fada
Wang, Zhuolu
Huang, Yun
Li, Jingdong
Wang, Zhiming
Li, Xinying - Abstract:
- Aim: To investigate the expression and clinical significance of ephrin type-A receptor 2 and epithelial-mesenchymal transition-related proteins in primary hepatocellular carcinoma. Methods: Tissues from 52 primary hepatocellular carcinomas and 12 human normal liver tissues were detected for expression of ephrin type-A receptor 2, E-cadherin, and N-cadherin by immunochemistry. Cinicopathological features of hepatocellular carcinoma and tumor recurrence after operation were studied for the association with these molecular expressions and E-N cadherin switch. Results: Increased expressions of ephrin type-A receptor 2 and N-cadherin and reduced expression of E-cadherin were significantly detected in hepatocellular carcinoma compared with normal liver tissues. Univariate analysis showed that there were close associations between unfavorable clinicopathological features and expressions of ephrin type-A receptor 2, E-cadherin, N-cadherin, and E-N cadherin switch. Ephrin type-A receptor 2 and E-cadherin expressions were confirmed as independent prognostic factors when corrected with age, gender, AFP, HBsAg, liver cirrhosis, tumor size, nodules, capsule, portal vein invasion, cell differentiation, and TNM stage. Conclusions: The overexpression of ephrin type-A receptor 2 protein is correlated with the number of tumors, capsular integrity, portal vein cancer thrombus and clinical stages. Epithelial-mesenchymal transition regulated by ephrin type-A receptor 2 is involved in theAim: To investigate the expression and clinical significance of ephrin type-A receptor 2 and epithelial-mesenchymal transition-related proteins in primary hepatocellular carcinoma. Methods: Tissues from 52 primary hepatocellular carcinomas and 12 human normal liver tissues were detected for expression of ephrin type-A receptor 2, E-cadherin, and N-cadherin by immunochemistry. Cinicopathological features of hepatocellular carcinoma and tumor recurrence after operation were studied for the association with these molecular expressions and E-N cadherin switch. Results: Increased expressions of ephrin type-A receptor 2 and N-cadherin and reduced expression of E-cadherin were significantly detected in hepatocellular carcinoma compared with normal liver tissues. Univariate analysis showed that there were close associations between unfavorable clinicopathological features and expressions of ephrin type-A receptor 2, E-cadherin, N-cadherin, and E-N cadherin switch. Ephrin type-A receptor 2 and E-cadherin expressions were confirmed as independent prognostic factors when corrected with age, gender, AFP, HBsAg, liver cirrhosis, tumor size, nodules, capsule, portal vein invasion, cell differentiation, and TNM stage. Conclusions: The overexpression of ephrin type-A receptor 2 protein is correlated with the number of tumors, capsular integrity, portal vein cancer thrombus and clinical stages. Epithelial-mesenchymal transition regulated by ephrin type-A receptor 2 is involved in the aggressive clinicopathological features and prognosis, suggesting that the receptor may play an important role in the progression and metastasis of hepatocellular carcinoma. … (more)
- Is Part Of:
- Tumori. Volume 99:Issue 6(2013)
- Journal:
- Tumori
- Issue:
- Volume 99:Issue 6(2013)
- Issue Display:
- Volume 99, Issue 6 (2013)
- Year:
- 2013
- Volume:
- 99
- Issue:
- 6
- Issue Sort Value:
- 2013-0099-0006-0000
- Page Start:
- 689
- Page End:
- 696
- Publication Date:
- 2013-11
- Subjects:
- E-cadherin -- ephrin type-A receptor 2 -- epithelial-mesenchymal transition -- N-cadherin -- primary hepatocellular carcinoma
Cancer -- Periodicals
616.994 - Journal URLs:
- http://catalog.hathitrust.org/api/volumes/oclc/1767840.html ↗
http://journals.sagepub.com/home/tmja ↗
http://www.tumorionline.it ↗
http://www.uk.sagepub.com/home.nav ↗ - DOI:
- 10.1177/030089161309900608 ↗
- Languages:
- English
- ISSNs:
- 0300-8916
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 25543.xml