Tumor-related gene expression levels in pulmonary pleomorphic carcinoma

被引:1
作者
Oyaizu, Takeshi [1 ]
Matsumura, Yuji [2 ]
Kobayashi, Satoru [1 ]
Sado, Tetsu [1 ]
Ishihama, Hiromi [1 ]
Chida, Masayuki [1 ]
机构
[1] Dokkyo Med Univ, Dept Gen Thorac Surg, Mibu, Tochigi 3210293, Japan
[2] Dokkyo Koshigaya Hosp, Dept Cardiovasc & Thorac Surg, Koshigaya, Saitama 3438555, Japan
关键词
Lung cancer; Pleomorphic carcinoma; Gene expression; CELL LUNG-CANCER; MESSENGER-RNA EXPRESSION; CHEMOTHERAPY; ERCC1; REPAIR;
D O I
10.1186/s13019-015-0282-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页数:5
相关论文
共 12 条
[1]  
[Anonymous], 2004, PATHOLOGY GENETICS T
[2]   Gene expression of ERCC1 as a novel prognostic marker in advanced bladder cancer patients receiving cisplatin-based chemotherapy [J].
Bellmunt, J. ;
Paz-Ares, L. ;
Cuello, M. ;
Cecere, F. L. ;
Albiol, S. ;
Guillem, V. ;
Gallardo, E. ;
Carles, J. ;
Mendez, P. ;
de la Cruz, J. J. ;
Taron, M. ;
Rosell, R. ;
Baselga, J. .
ANNALS OF ONCOLOGY, 2007, 18 (03) :522-528
[3]   Customizing cisplatin based on quantitative excision repair cross-complementing 1 mRNA expression:: A phase III trial in non-small-cell lung cancer [J].
Cobo, Manuel ;
Isla, Dolores ;
Massuti, Bartomeu ;
Montes, Ana ;
Miguel Sanchez, Jose ;
Provencio, Mariano ;
Vinolas, Nuria ;
Paz-Ares, Luis ;
Lopez-Vivanco, Guillermo ;
Angel Munoz, Miguel ;
Felip, Enriqueta ;
Alberola, Vicente ;
Camps, Carlos ;
Domine, Manuel ;
Sanchez, Jose Javier ;
Sanchez-Ronco, Maria ;
Danenberg, Kathleen ;
Taron, Miquel ;
Gandara, David ;
Rosell, Rafael .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (19) :2747-2754
[4]   Pulmonary sarcomatoid carcinoma: a clinicopathologic study and prognostic analysis of 51 cases [J].
Huang, Si-Yuan ;
Shen, Shu-Jing ;
Li, Xing-Ya .
WORLD JOURNAL OF SURGICAL ONCOLOGY, 2013, 11
[5]   Comparison of 5-Fluorouracil-related Gene Expression Levels Between Adenocarcinomas and Squamous Cell Carcinomas of the Lung [J].
Ishihama, Hiromi ;
Chida, Masayuki ;
Araki, Osamu ;
Karube, Yoko ;
Seki, Norio ;
Tamura, Motohiko ;
Umezu, Hideo ;
Honma, Koichi ;
Masawa, Nobuhide ;
Miyoshi, Shinichiro .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2009, 39 (01) :33-36
[6]  
Karube Y, 2013, NIPHON GEKAGAKKAI S2, V114, P730
[7]  
Kawano R, 2008, HAIGAN JPN J LUNG CA, V48, P106
[8]  
Kuramochi H, 2006, CLIN CANCER RES, V12, P29, DOI 10.1158/1078-0432.CCR-05-1275
[9]  
Lord RVN, 2002, CLIN CANCER RES, V8, P2286
[10]   DNA repair by ERCC1 in non-small-cell lung cancer and cisplatin-based adjuvant chemotherapy [J].
Olaussen, Ken A. ;
Dunant, Ariane ;
Fouret, Pierre ;
Brambilla, Elisabeth ;
Andre, Fabrice ;
Haddad, Vincent ;
Taranchon, Estelle ;
Filipits, Martin ;
Pirker, Robert ;
Popper, Helmut H. ;
Stahel, Rolf ;
Sabatier, Laure ;
Pignon, Jean-Pierre ;
Tursz, Thomas ;
Le Chevalier, Thierry ;
Soria, Jean-Charles .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (10) :983-991