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CLCA2 as a Novel Immunohistochemical Marker for Differential Diagnosis of Squamous Cell Carcinoma from Adenocarcinoma of the Lung
Recent progress in targeted therapy for lung cancer has revealed that accurate differential diagnosis between squamous cell carcinoma (SCC) and adenocarcinoma (ADC) of the lung is essential. To identify a novel immunohistochemical marker useful for differential diagnosis between the two subtypes of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274868/ https://www.ncbi.nlm.nih.gov/pubmed/25548429 http://dx.doi.org/10.1155/2014/619273 |
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author | Shinmura, Kazuya Igarashi, Hisaki Kato, Hisami Kawanishi, Yuichi Inoue, Yusuke Nakamura, Satoki Ogawa, Hiroshi Yamashita, Takashi Kawase, Akikazu Funai, Kazuhito Sugimura, Haruhiko |
author_facet | Shinmura, Kazuya Igarashi, Hisaki Kato, Hisami Kawanishi, Yuichi Inoue, Yusuke Nakamura, Satoki Ogawa, Hiroshi Yamashita, Takashi Kawase, Akikazu Funai, Kazuhito Sugimura, Haruhiko |
author_sort | Shinmura, Kazuya |
collection | PubMed |
description | Recent progress in targeted therapy for lung cancer has revealed that accurate differential diagnosis between squamous cell carcinoma (SCC) and adenocarcinoma (ADC) of the lung is essential. To identify a novel immunohistochemical marker useful for differential diagnosis between the two subtypes of lung cancer, we first selected 24 SCC-specific genes and 6 ADC-specific genes using data (case number, 980) from the Cancer Genome Atlas (TCGA) database. Among the genes, we chose the CLCA2 gene, which is involved in chloride conductance and whose protein expression in lung cancer is yet to be characterized, and evaluated its protein expression status in 396 cases of primary lung cancer at Hamamatsu University Hospital. Immunohistochemical analysis revealed a significantly higher CLCA2 expression level in the SCCs than in the ADCs (P < 0.0001) and also a significantly higher frequency of CLCA2 protein expression in the SCCs (104/161, 64.6%) as compared with that in the ADCs (2/235, 0.9%) (P < 0.0001; sensitivity 64.6%, specificity 99.1%). The CLCA2 protein expression status was associated with the histological tumor grade in the SCCs. These results suggest that CLCA2 might be a novel excellent immunohistochemical marker for differentiating between primary SCC and primary ADC of the lung. |
format | Online Article Text |
id | pubmed-4274868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42748682014-12-29 CLCA2 as a Novel Immunohistochemical Marker for Differential Diagnosis of Squamous Cell Carcinoma from Adenocarcinoma of the Lung Shinmura, Kazuya Igarashi, Hisaki Kato, Hisami Kawanishi, Yuichi Inoue, Yusuke Nakamura, Satoki Ogawa, Hiroshi Yamashita, Takashi Kawase, Akikazu Funai, Kazuhito Sugimura, Haruhiko Dis Markers Research Article Recent progress in targeted therapy for lung cancer has revealed that accurate differential diagnosis between squamous cell carcinoma (SCC) and adenocarcinoma (ADC) of the lung is essential. To identify a novel immunohistochemical marker useful for differential diagnosis between the two subtypes of lung cancer, we first selected 24 SCC-specific genes and 6 ADC-specific genes using data (case number, 980) from the Cancer Genome Atlas (TCGA) database. Among the genes, we chose the CLCA2 gene, which is involved in chloride conductance and whose protein expression in lung cancer is yet to be characterized, and evaluated its protein expression status in 396 cases of primary lung cancer at Hamamatsu University Hospital. Immunohistochemical analysis revealed a significantly higher CLCA2 expression level in the SCCs than in the ADCs (P < 0.0001) and also a significantly higher frequency of CLCA2 protein expression in the SCCs (104/161, 64.6%) as compared with that in the ADCs (2/235, 0.9%) (P < 0.0001; sensitivity 64.6%, specificity 99.1%). The CLCA2 protein expression status was associated with the histological tumor grade in the SCCs. These results suggest that CLCA2 might be a novel excellent immunohistochemical marker for differentiating between primary SCC and primary ADC of the lung. Hindawi Publishing Corporation 2014 2014-12-07 /pmc/articles/PMC4274868/ /pubmed/25548429 http://dx.doi.org/10.1155/2014/619273 Text en Copyright © 2014 Kazuya Shinmura et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Shinmura, Kazuya Igarashi, Hisaki Kato, Hisami Kawanishi, Yuichi Inoue, Yusuke Nakamura, Satoki Ogawa, Hiroshi Yamashita, Takashi Kawase, Akikazu Funai, Kazuhito Sugimura, Haruhiko CLCA2 as a Novel Immunohistochemical Marker for Differential Diagnosis of Squamous Cell Carcinoma from Adenocarcinoma of the Lung |
title | CLCA2 as a Novel Immunohistochemical Marker for Differential Diagnosis of Squamous Cell Carcinoma from Adenocarcinoma of the Lung |
title_full | CLCA2 as a Novel Immunohistochemical Marker for Differential Diagnosis of Squamous Cell Carcinoma from Adenocarcinoma of the Lung |
title_fullStr | CLCA2 as a Novel Immunohistochemical Marker for Differential Diagnosis of Squamous Cell Carcinoma from Adenocarcinoma of the Lung |
title_full_unstemmed | CLCA2 as a Novel Immunohistochemical Marker for Differential Diagnosis of Squamous Cell Carcinoma from Adenocarcinoma of the Lung |
title_short | CLCA2 as a Novel Immunohistochemical Marker for Differential Diagnosis of Squamous Cell Carcinoma from Adenocarcinoma of the Lung |
title_sort | clca2 as a novel immunohistochemical marker for differential diagnosis of squamous cell carcinoma from adenocarcinoma of the lung |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274868/ https://www.ncbi.nlm.nih.gov/pubmed/25548429 http://dx.doi.org/10.1155/2014/619273 |
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