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Tumor-related gene expression levels in pulmonary pleomorphic carcinoma
BACKGROUND: Pulmonary pleomorphic carcinoma (PPC) is a rare type of non-small-cell lung cancer that belongs to the family of sarcomatoid carcinomas and is associated with poor prognosis. We investigated the expressions of tumor-related genes in resected PPC specimens. METHODS: Specimens resected fro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465152/ https://www.ncbi.nlm.nih.gov/pubmed/26031756 http://dx.doi.org/10.1186/s13019-015-0282-1 |
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author | Oyaizu, Takeshi Matsumura, Yuji Kobayashi, Satoru Sado, Tetsu Ishihama, Hiromi Chida, Masayuki |
author_facet | Oyaizu, Takeshi Matsumura, Yuji Kobayashi, Satoru Sado, Tetsu Ishihama, Hiromi Chida, Masayuki |
author_sort | Oyaizu, Takeshi |
collection | PubMed |
description | BACKGROUND: Pulmonary pleomorphic carcinoma (PPC) is a rare type of non-small-cell lung cancer that belongs to the family of sarcomatoid carcinomas and is associated with poor prognosis. We investigated the expressions of tumor-related genes in resected PPC specimens. METHODS: Specimens resected from patients with PPC from July 2006 through April 2012 were investigated. Tumor segments were collected from the specimens by micro-dissection to extract mRNA, then RT-PCR was performed according to Dannenberg’s tumor profile method for semi-quantitation of tumor-related gene mRNA. To compare with other types of lung cancer, data from stage-matched adenocarcinoma (AC) and squamous cell carcinoma (SCC) cases in our database were also examined. RESULTS: The gene expression levels of thymidylate synthase were significantly higher in PPC and SCC as compared to the AC specimens (p < 0.001). The levels of dihydropyrimidine dehydrogenase and thymidine phosphorylase mRNA in PPC showed a similar tendency to those in SCC, in contrast to AC. Furthermore, the expression level of excision repair cross-complementation group 1 mRNA in PPC specimens was similar to that reported in NSCLC, while the level of vascular endothelial growth factor (VEGF) expression was higher as compared to that reported for colorectal cancer. CONCLUSIONS: Although gene expression of tumor cannot be directly correlated to its sensitivity for anti-cancer drugs, it is likely that PPC tumors are not sensitive to anti-metabolic drugs. Anti-VEGF therapy may be a candidate for PPC, while cisplatin also remains a viable option. |
format | Online Article Text |
id | pubmed-4465152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44651522015-06-14 Tumor-related gene expression levels in pulmonary pleomorphic carcinoma Oyaizu, Takeshi Matsumura, Yuji Kobayashi, Satoru Sado, Tetsu Ishihama, Hiromi Chida, Masayuki J Cardiothorac Surg Research Article BACKGROUND: Pulmonary pleomorphic carcinoma (PPC) is a rare type of non-small-cell lung cancer that belongs to the family of sarcomatoid carcinomas and is associated with poor prognosis. We investigated the expressions of tumor-related genes in resected PPC specimens. METHODS: Specimens resected from patients with PPC from July 2006 through April 2012 were investigated. Tumor segments were collected from the specimens by micro-dissection to extract mRNA, then RT-PCR was performed according to Dannenberg’s tumor profile method for semi-quantitation of tumor-related gene mRNA. To compare with other types of lung cancer, data from stage-matched adenocarcinoma (AC) and squamous cell carcinoma (SCC) cases in our database were also examined. RESULTS: The gene expression levels of thymidylate synthase were significantly higher in PPC and SCC as compared to the AC specimens (p < 0.001). The levels of dihydropyrimidine dehydrogenase and thymidine phosphorylase mRNA in PPC showed a similar tendency to those in SCC, in contrast to AC. Furthermore, the expression level of excision repair cross-complementation group 1 mRNA in PPC specimens was similar to that reported in NSCLC, while the level of vascular endothelial growth factor (VEGF) expression was higher as compared to that reported for colorectal cancer. CONCLUSIONS: Although gene expression of tumor cannot be directly correlated to its sensitivity for anti-cancer drugs, it is likely that PPC tumors are not sensitive to anti-metabolic drugs. Anti-VEGF therapy may be a candidate for PPC, while cisplatin also remains a viable option. BioMed Central 2015-06-03 /pmc/articles/PMC4465152/ /pubmed/26031756 http://dx.doi.org/10.1186/s13019-015-0282-1 Text en © Oyaizu et al. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Oyaizu, Takeshi Matsumura, Yuji Kobayashi, Satoru Sado, Tetsu Ishihama, Hiromi Chida, Masayuki Tumor-related gene expression levels in pulmonary pleomorphic carcinoma |
title | Tumor-related gene expression levels in pulmonary pleomorphic carcinoma |
title_full | Tumor-related gene expression levels in pulmonary pleomorphic carcinoma |
title_fullStr | Tumor-related gene expression levels in pulmonary pleomorphic carcinoma |
title_full_unstemmed | Tumor-related gene expression levels in pulmonary pleomorphic carcinoma |
title_short | Tumor-related gene expression levels in pulmonary pleomorphic carcinoma |
title_sort | tumor-related gene expression levels in pulmonary pleomorphic carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465152/ https://www.ncbi.nlm.nih.gov/pubmed/26031756 http://dx.doi.org/10.1186/s13019-015-0282-1 |
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