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- PMID: 16083620
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Article: Expressions of E-cadherin in non-small cell lung cancer and it correlation with prognosis
Title | Expressions of E-cadherin in non-small cell lung cancer and it correlation with prognosis |
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Authors | |
Issue Date | 2005 |
Citation | Zhonghua Wai Ke Za Zhi [Chinese Journal Of Surgery], 2005, v. 43 n. 14, p. 913-917 How to Cite? |
Abstract | OBJECTIVE: This study was to clarify E-cadherin expressions in non-small cell lung cancer (NSCLC) and its correlation with patients' prognosis. METHODS: Tissue microarrays (TMAs) containing specimens from 365 different NSCLC were constructed, covering all stages and almost all histological types of this disease. Slides were immunohistochemically stained with antibodies against E-cadherin. Expression pattern of the protein was analyzed with relation to the clinicopathological. Correlations of the results with patients' overall survival were also examined. RESULTS: Immunohistochemical staining revealed that E-cadherin protein was localized mainly on membranes and the cytoplasm of NSCLC tumors cells. Reduced E-cadherin expression was evident in 32.1%. Reduced E-cadherin expression significantly correlated with lymph nodes metastasis (chi(2) = 16.430, P = 0.001), histological dedifferentiation (chi(2) = 9.243, P = 0.010) and advanced clinical stage (chi(2) = 9.421, P = 0.024). There was no significant difference in E-cadherin expression between squamous cell carcinoma and adenocarcinoma. E-cadherin reduced expression correlated with a poor prognosis (P < 0.0001) in univariate analysis. Multivariate analysis showed a significantly lower survival probability for patients with reduced E-cadherin (P < 0.001), and E-cadherin was an independent prognostic factor for survival of NSCLC patients. CONCLUSIONS: It suggests that dysfunction of E-cadherin has an important impact in the progression of lung cancer. As an independent prognostic factor, expression of E-cadherin can predict outcome of different group, together with conventional prognostic factors, and subsequently make appropriate management. |
Persistent Identifier | http://hdl.handle.net/10722/150813 |
ISSN | 2023 SCImago Journal Rankings: 0.159 |
DC Field | Value | Language |
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dc.contributor.author | Qiao, GB | en_US |
dc.contributor.author | Wu, YL | en_US |
dc.contributor.author | Ou, W | en_US |
dc.contributor.author | Yang, XN | en_US |
dc.contributor.author | Zhong, WZ | en_US |
dc.contributor.author | Lin, JY | en_US |
dc.contributor.author | Zhao, J | en_US |
dc.contributor.author | Xie, D | en_US |
dc.contributor.author | Guan, XY | en_US |
dc.date.accessioned | 2012-06-26T06:11:03Z | - |
dc.date.available | 2012-06-26T06:11:03Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.citation | Zhonghua Wai Ke Za Zhi [Chinese Journal Of Surgery], 2005, v. 43 n. 14, p. 913-917 | en_US |
dc.identifier.issn | 0529-5815 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/150813 | - |
dc.description.abstract | OBJECTIVE: This study was to clarify E-cadherin expressions in non-small cell lung cancer (NSCLC) and its correlation with patients' prognosis. METHODS: Tissue microarrays (TMAs) containing specimens from 365 different NSCLC were constructed, covering all stages and almost all histological types of this disease. Slides were immunohistochemically stained with antibodies against E-cadherin. Expression pattern of the protein was analyzed with relation to the clinicopathological. Correlations of the results with patients' overall survival were also examined. RESULTS: Immunohistochemical staining revealed that E-cadherin protein was localized mainly on membranes and the cytoplasm of NSCLC tumors cells. Reduced E-cadherin expression was evident in 32.1%. Reduced E-cadherin expression significantly correlated with lymph nodes metastasis (chi(2) = 16.430, P = 0.001), histological dedifferentiation (chi(2) = 9.243, P = 0.010) and advanced clinical stage (chi(2) = 9.421, P = 0.024). There was no significant difference in E-cadherin expression between squamous cell carcinoma and adenocarcinoma. E-cadherin reduced expression correlated with a poor prognosis (P < 0.0001) in univariate analysis. Multivariate analysis showed a significantly lower survival probability for patients with reduced E-cadherin (P < 0.001), and E-cadherin was an independent prognostic factor for survival of NSCLC patients. CONCLUSIONS: It suggests that dysfunction of E-cadherin has an important impact in the progression of lung cancer. As an independent prognostic factor, expression of E-cadherin can predict outcome of different group, together with conventional prognostic factors, and subsequently make appropriate management. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Zhonghua wai ke za zhi [Chinese journal of surgery] | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Aged, 80 And Over | en_US |
dc.subject.mesh | Cadherins - Biosynthesis | en_US |
dc.subject.mesh | Carcinoma, Non-Small-Cell Lung - Metabolism - Mortality - Secondary | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Follow-Up Studies | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | Lung Neoplasms - Metabolism - Mortality - Pathology | en_US |
dc.subject.mesh | Lymphatic Metastasis | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Neoplasm Staging | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Survival Rate | en_US |
dc.title | Expressions of E-cadherin in non-small cell lung cancer and it correlation with prognosis | en_US |
dc.type | Article | en_US |
dc.identifier.email | Guan, XY:xyguan@hkucc.hku.hk | en_US |
dc.identifier.authority | Guan, XY=rp00454 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.pmid | 16083620 | - |
dc.identifier.scopus | eid_2-s2.0-39049183042 | en_US |
dc.identifier.volume | 43 | en_US |
dc.identifier.issue | 14 | en_US |
dc.identifier.spage | 913 | en_US |
dc.identifier.epage | 917 | en_US |
dc.identifier.scopusauthorid | Qiao, GB=8318743700 | en_US |
dc.identifier.scopusauthorid | Wu, YL=8974511600 | en_US |
dc.identifier.scopusauthorid | Ou, W=7007123676 | en_US |
dc.identifier.scopusauthorid | Yang, XN=8318743600 | en_US |
dc.identifier.scopusauthorid | Zhong, WZ=16065101400 | en_US |
dc.identifier.scopusauthorid | Lin, JY=26028341200 | en_US |
dc.identifier.scopusauthorid | Zhao, J=7410312185 | en_US |
dc.identifier.scopusauthorid | Xie, D=35070710200 | en_US |
dc.identifier.scopusauthorid | Guan, XY=7201463221 | en_US |
dc.identifier.issnl | 0529-5815 | - |