Analysis of an EGFR mutation by PNA clamping method in lung carcinoid tumors.
10.7180/kmj.2015.30.2.141
- Author:
Jong In KIM
1
Author Information
1. Department of Thoracic and Cardiovascular Surgery, College of Medicine, Kosin University, Busan, Korea. schoi@ns.kosinmed.or.kr
- Publication Type:Original Article
- Keywords:
carcinoid;
EGFR mutation;
Lung;
PNA clamping
- MeSH:
Carcinoid Tumor*;
Constriction*;
Genotype;
Lung*;
Neoplasm Metastasis;
Polymerase Chain Reaction
- From:Kosin Medical Journal
2015;30(2):141-147
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Pulmonary carcinoid tumors consisting of typical carcinoid tumors (TC) and atypical carcinoid tumors (AC) are rare, accounting for 2-5% of all lung tumors. TC is considered a low-grade tumor with a rate of distant metastasis up to 12%. In contrast, ACs are more aggressive tumors, displaying a metastatic rate up to 70%. Surgery is the treatment of choice; however, the current treatment outcomes of metastatic lung carcinoids are discouraging. This study aimed to investigate the EGFR mutation using the PNA-mediated clamping method and to provide basic data for using EGFR-TK1 and its clinical implications. MATERIALS AND METHODS: A total of 14 cases that underwent surgery were diagnosed as carcinoid tumors and pathologically classified as TC and AC. The paraffin-embedded tissues were analyzed for EGFR mutations using the PNA-mediated PCR clamping technique. The mutant type was noted in the cases with a DeltaCt greater than 2.0. RESULT: Of 14 cases, eight were AC and six cases were TC. No known EGFR mutation was detected with a DeltaCt less than 2.0. CONCLUSION: The EGFR genotype determined using the PNA-mediated PCR clamping method was wild-type in all pulmonary carcinoid tumors. Therefore, the application of EGFR-TK1 is limited in pulmonary carcinoid tumors.
