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c-Cbl、Cbl-b和EGFR在非小细胞肺癌中的表达及其预后价值
BACKGROUND AND OBJECTIVE: Epidermal growth factor receptor (EGFR) is closely correlated with the progression of lung cancer. Its activity is modulated by Casitas B-lineage lymphoma (Cbl) family. The aim of this study is to investigate the expression and clinical relevance of c-Cbl, Cbl-b and EGFR in...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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中国肺癌杂志编辑部
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999894/ https://www.ncbi.nlm.nih.gov/pubmed/21645455 http://dx.doi.org/10.3779/j.issn.1009-3419.2011.06.17 |
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collection | PubMed |
description | BACKGROUND AND OBJECTIVE: Epidermal growth factor receptor (EGFR) is closely correlated with the progression of lung cancer. Its activity is modulated by Casitas B-lineage lymphoma (Cbl) family. The aim of this study is to investigate the expression and clinical relevance of c-Cbl, Cbl-b and EGFR in non-small cell lung cancer (NSCLC). METHODS: Expressions of c-Cbl, Cbl-b and EGFR protein were detected with tissue microarrays and immunohistochemistry technique in 94 cases of NSCLC. The correlations between the expression of the three proteins and clinicopathological parameters were analyzed. RESULTS: The positive expression rates of EGFR, c-Cbl and Cbl-b were 60.6% (57/94), 30.9% (29/94) and 84.0% (79/94), respectively. The expression of EGFR, c-Cbl and Cbl-b was not associated with age, pathological type, TNM stage, lymph node metastasis, and smoking history. c-Cbl and Cbl-b status was not significantly correlated with overall survival. Subgroup analyses showed that c-Cbl-positive patients had longer survival than c-Cbl-negative patients in EGFR-positive group (P=0.014). CONCLUSION: Detection of c-Cbl protein levels might contribute to the prognosis evaluation of EGFR-positive NSCLC. |
format | Online Article Text |
id | pubmed-5999894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | 中国肺癌杂志编辑部 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59998942018-07-06 c-Cbl、Cbl-b和EGFR在非小细胞肺癌中的表达及其预后价值 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: Epidermal growth factor receptor (EGFR) is closely correlated with the progression of lung cancer. Its activity is modulated by Casitas B-lineage lymphoma (Cbl) family. The aim of this study is to investigate the expression and clinical relevance of c-Cbl, Cbl-b and EGFR in non-small cell lung cancer (NSCLC). METHODS: Expressions of c-Cbl, Cbl-b and EGFR protein were detected with tissue microarrays and immunohistochemistry technique in 94 cases of NSCLC. The correlations between the expression of the three proteins and clinicopathological parameters were analyzed. RESULTS: The positive expression rates of EGFR, c-Cbl and Cbl-b were 60.6% (57/94), 30.9% (29/94) and 84.0% (79/94), respectively. The expression of EGFR, c-Cbl and Cbl-b was not associated with age, pathological type, TNM stage, lymph node metastasis, and smoking history. c-Cbl and Cbl-b status was not significantly correlated with overall survival. Subgroup analyses showed that c-Cbl-positive patients had longer survival than c-Cbl-negative patients in EGFR-positive group (P=0.014). CONCLUSION: Detection of c-Cbl protein levels might contribute to the prognosis evaluation of EGFR-positive NSCLC. 中国肺癌杂志编辑部 2011-06-20 /pmc/articles/PMC5999894/ /pubmed/21645455 http://dx.doi.org/10.3779/j.issn.1009-3419.2011.06.17 Text en 版权所有©《中国肺癌杂志》编辑部2011 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | 临床研究 c-Cbl、Cbl-b和EGFR在非小细胞肺癌中的表达及其预后价值 |
title | c-Cbl、Cbl-b和EGFR在非小细胞肺癌中的表达及其预后价值 |
title_full | c-Cbl、Cbl-b和EGFR在非小细胞肺癌中的表达及其预后价值 |
title_fullStr | c-Cbl、Cbl-b和EGFR在非小细胞肺癌中的表达及其预后价值 |
title_full_unstemmed | c-Cbl、Cbl-b和EGFR在非小细胞肺癌中的表达及其预后价值 |
title_short | c-Cbl、Cbl-b和EGFR在非小细胞肺癌中的表达及其预后价值 |
title_sort | c-cbl、cbl-b和egfr在非小细胞肺癌中的表达及其预后价值 |
topic | 临床研究 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999894/ https://www.ncbi.nlm.nih.gov/pubmed/21645455 http://dx.doi.org/10.3779/j.issn.1009-3419.2011.06.17 |
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