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A favourable prognostic marker for EGFR mutant non-small cell lung cancer: immunohistochemical analysis of MUC5B

OBJECTIVES: To determine the use of the mucin proteins MUC5B and MUC5AC as prognosis markers for non-small cell lung cancer (NSCLC) carrying epidermal growth factor receptor (EGFR) mutations. SETTING: Patients who underwent surgical resection at Nagasaki University Hospital and related facilities in...

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Autores principales: Wakata, Kouki, Tsuchiya, Tomoshi, Tomoshige, Koichi, Takagi, Katsunori, Yamasaki, Naoya, Matsumoto, Keitaro, Miyazaki, Takuro, Nanashima, Atsushi, Whitsett, Jeffrey A, Maeda, Yutaka, Nagayasu, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521511/
https://www.ncbi.nlm.nih.gov/pubmed/26224019
http://dx.doi.org/10.1136/bmjopen-2015-008366
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author Wakata, Kouki
Tsuchiya, Tomoshi
Tomoshige, Koichi
Takagi, Katsunori
Yamasaki, Naoya
Matsumoto, Keitaro
Miyazaki, Takuro
Nanashima, Atsushi
Whitsett, Jeffrey A
Maeda, Yutaka
Nagayasu, Takeshi
author_facet Wakata, Kouki
Tsuchiya, Tomoshi
Tomoshige, Koichi
Takagi, Katsunori
Yamasaki, Naoya
Matsumoto, Keitaro
Miyazaki, Takuro
Nanashima, Atsushi
Whitsett, Jeffrey A
Maeda, Yutaka
Nagayasu, Takeshi
author_sort Wakata, Kouki
collection PubMed
description OBJECTIVES: To determine the use of the mucin proteins MUC5B and MUC5AC as prognosis markers for non-small cell lung cancer (NSCLC) carrying epidermal growth factor receptor (EGFR) mutations. SETTING: Patients who underwent surgical resection at Nagasaki University Hospital and related facilities in Japan between June 1996 and March 2013. PARTICIPANT: 159 Japanese patients (male: n=103; female: n=56) with NSCLC, who underwent surgical resection (EGFR-mutant type: n=78, EGFR wild type: n=81). RESULTS: Patients whose tumours expressed MUC5B had significantly longer overall survival and relapse-free survival compared to the MUC5B-negative patients with EGFR mutant NSCLC (p=0.0098 and p=0.0187, respectively). In patients with EGFR wild-type NSCLC, there was no association with MUC5B expression. MUC5AC expression was not different between EGFR mutant and wild-type NSCLC. CONCLUSIONS: Present findings indicate that MUC5B, but not MUC5AC, is a novel prognostic biomarker for patients with NSCLC carrying EGFR mutations but not for patients with NSCLC carrying wild-type EGFR.
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spelling pubmed-45215112015-08-05 A favourable prognostic marker for EGFR mutant non-small cell lung cancer: immunohistochemical analysis of MUC5B Wakata, Kouki Tsuchiya, Tomoshi Tomoshige, Koichi Takagi, Katsunori Yamasaki, Naoya Matsumoto, Keitaro Miyazaki, Takuro Nanashima, Atsushi Whitsett, Jeffrey A Maeda, Yutaka Nagayasu, Takeshi BMJ Open Oncology OBJECTIVES: To determine the use of the mucin proteins MUC5B and MUC5AC as prognosis markers for non-small cell lung cancer (NSCLC) carrying epidermal growth factor receptor (EGFR) mutations. SETTING: Patients who underwent surgical resection at Nagasaki University Hospital and related facilities in Japan between June 1996 and March 2013. PARTICIPANT: 159 Japanese patients (male: n=103; female: n=56) with NSCLC, who underwent surgical resection (EGFR-mutant type: n=78, EGFR wild type: n=81). RESULTS: Patients whose tumours expressed MUC5B had significantly longer overall survival and relapse-free survival compared to the MUC5B-negative patients with EGFR mutant NSCLC (p=0.0098 and p=0.0187, respectively). In patients with EGFR wild-type NSCLC, there was no association with MUC5B expression. MUC5AC expression was not different between EGFR mutant and wild-type NSCLC. CONCLUSIONS: Present findings indicate that MUC5B, but not MUC5AC, is a novel prognostic biomarker for patients with NSCLC carrying EGFR mutations but not for patients with NSCLC carrying wild-type EGFR. BMJ Publishing Group 2015-07-29 /pmc/articles/PMC4521511/ /pubmed/26224019 http://dx.doi.org/10.1136/bmjopen-2015-008366 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Oncology
Wakata, Kouki
Tsuchiya, Tomoshi
Tomoshige, Koichi
Takagi, Katsunori
Yamasaki, Naoya
Matsumoto, Keitaro
Miyazaki, Takuro
Nanashima, Atsushi
Whitsett, Jeffrey A
Maeda, Yutaka
Nagayasu, Takeshi
A favourable prognostic marker for EGFR mutant non-small cell lung cancer: immunohistochemical analysis of MUC5B
title A favourable prognostic marker for EGFR mutant non-small cell lung cancer: immunohistochemical analysis of MUC5B
title_full A favourable prognostic marker for EGFR mutant non-small cell lung cancer: immunohistochemical analysis of MUC5B
title_fullStr A favourable prognostic marker for EGFR mutant non-small cell lung cancer: immunohistochemical analysis of MUC5B
title_full_unstemmed A favourable prognostic marker for EGFR mutant non-small cell lung cancer: immunohistochemical analysis of MUC5B
title_short A favourable prognostic marker for EGFR mutant non-small cell lung cancer: immunohistochemical analysis of MUC5B
title_sort favourable prognostic marker for egfr mutant non-small cell lung cancer: immunohistochemical analysis of muc5b
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521511/
https://www.ncbi.nlm.nih.gov/pubmed/26224019
http://dx.doi.org/10.1136/bmjopen-2015-008366
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