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This article is part of the supplement: Abstracts of the 16th International Charles Heidelberger Symposium on Cancer Research

Open Access Poster presentation

KRAS and EGFR mutations coexisting in lung adenocarcinoma

Vitor Sousa1234*, Ana Alarcão12, Patricia Couceiro12, Maria R Silva13, Maria J d’Aguiar1, Lia Teixeira1 and Lina Carvalho1234

Author Affiliations

1 Instituto de Anatomia Patológica, Faculdade de Medicina da Universidade de Coimbra, Coimbra, Portugal

2 Centro de Investigação em Meio Ambiente, Genética e Oncobiologia (CIMAGO), Coimbra, Portugal

3 Centro de Pneumologia, Faculdade de Medicina da Universidade de Coimbra, Coimbra, Portugal

4 Serviço de Anatomia Patológica dos Hospitais da Universidade de Coimbra, Coimbra, Portugal

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BMC Proceedings 2010, 4(Suppl 2):P57  doi:10.1186/1753-6561-4-S2-P57


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1753-6561/4/S2/P57


Published:24 September 2010

© 2010 Sousa et al; licensee BioMed Central Ltd.

Poster presentation

Lung adenocarcinoma represents about 42% and 28% of NSCLC in women and men. Adenocarcinomas incidence is still rising being the most frequent type of NSCLC diagnosed in USA. Both EGFR and KRAS gene mutations can contribute to the development of NSCLC, namely adenocarcinomas. EGFR and KRAS mutations are considered by some authors as mutually exclusive explained by the fact that KRAS-MAPK pathway is one of the downstream signalling pathways of EGFR. Lung cancers with KRAS mutations are resistant to EGFR tyrosine kinase inhibitors.

Sections of the adenocarcinoma of the lung, formalin-fixed paraffin-embedded tissues (FFPE), were selected to analyze mutations in EGFR exons 19 and 21 and KRAS - codons 12 and 13 by DNA extraction for polymerase chain reaction (PCR). Exon 19 was studied by fragment analysis and exon 21, codons 12 and 13 were studied by direct sequencing. The analysis of FISH results was done by Cappuzzo’s score to EGFR gene. Determination of EGFR protein expression was done by immunohistochemistry (IHC) (Zymed Laboratories).

The authors present a rare case with synchronous EGFR and KRAS mutations. The patient is a 77 years old, male with a central 3cm mixed adenocarcinoma. The tumor showed EGFR protein overexpression identified by IHC and chromosome 7 high polyssomy by FISH.

The authors call attention to the fact that although EGFR and KRAS mutations are almost always mutually exclusive in some cases they may coexist in the same neoplasia.