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Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC

In non-small-cell lung cancer (NSCLC), epidermal growth factor receptor (EGFR) and K-RAS mutations of the primary tumour are associated with responsiveness and resistance to tyrosine kinase inhibitors (TKIs), respectively. However, the EGFR and K-RAS mutation status in metastases is not well studied...

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Autores principales: Kalikaki, A, Koutsopoulos, A, Trypaki, M, Souglakos, J, Stathopoulos, E, Georgoulias, V, Mavroudis, D, Voutsina, A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538768/
https://www.ncbi.nlm.nih.gov/pubmed/19238633
http://dx.doi.org/10.1038/sj.bjc.6604629
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author Kalikaki, A
Koutsopoulos, A
Trypaki, M
Souglakos, J
Stathopoulos, E
Georgoulias, V
Mavroudis, D
Voutsina, A
author_facet Kalikaki, A
Koutsopoulos, A
Trypaki, M
Souglakos, J
Stathopoulos, E
Georgoulias, V
Mavroudis, D
Voutsina, A
author_sort Kalikaki, A
collection PubMed
description In non-small-cell lung cancer (NSCLC), epidermal growth factor receptor (EGFR) and K-RAS mutations of the primary tumour are associated with responsiveness and resistance to tyrosine kinase inhibitors (TKIs), respectively. However, the EGFR and K-RAS mutation status in metastases is not well studied. We compared the mutation status of these genes between the primary tumours and the corresponding metastases of 25 patients. Epidermal growth factor receptor and K-RAS mutation status was different between primary tumours and corresponding metastases in 7 (28%) and 6 (24%) of the 25 patients, respectively. Among the 25 primary tumours, three ‘hotspot’ and two non-classical EGFR mutations were found; none of the corresponding metastases had the same mutation pattern. Among the five (20%) K-RAS mutations detected in the primary tumours, two were maintained in the corresponding metastasis. Epidermal growth factor receptor and K-RAS mutations were detected in the metastatic tumours of three (12%) and five (20%) patients, respectively. The expressions of EGFR and phosphorylated EGFR showed 10 and 50% discordance, in that order. We conclude that there is substantial discordance in EGFR and K-RAS mutational status between the primary tumours and corresponding metastases in patients with NSCLC and this might have therapeutic implications when treatment with TKIs is considered.
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spelling pubmed-25387682009-09-16 Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC Kalikaki, A Koutsopoulos, A Trypaki, M Souglakos, J Stathopoulos, E Georgoulias, V Mavroudis, D Voutsina, A Br J Cancer Molecular Diagnostics In non-small-cell lung cancer (NSCLC), epidermal growth factor receptor (EGFR) and K-RAS mutations of the primary tumour are associated with responsiveness and resistance to tyrosine kinase inhibitors (TKIs), respectively. However, the EGFR and K-RAS mutation status in metastases is not well studied. We compared the mutation status of these genes between the primary tumours and the corresponding metastases of 25 patients. Epidermal growth factor receptor and K-RAS mutation status was different between primary tumours and corresponding metastases in 7 (28%) and 6 (24%) of the 25 patients, respectively. Among the 25 primary tumours, three ‘hotspot’ and two non-classical EGFR mutations were found; none of the corresponding metastases had the same mutation pattern. Among the five (20%) K-RAS mutations detected in the primary tumours, two were maintained in the corresponding metastasis. Epidermal growth factor receptor and K-RAS mutations were detected in the metastatic tumours of three (12%) and five (20%) patients, respectively. The expressions of EGFR and phosphorylated EGFR showed 10 and 50% discordance, in that order. We conclude that there is substantial discordance in EGFR and K-RAS mutational status between the primary tumours and corresponding metastases in patients with NSCLC and this might have therapeutic implications when treatment with TKIs is considered. Nature Publishing Group 2008-09-16 2008-08-26 /pmc/articles/PMC2538768/ /pubmed/19238633 http://dx.doi.org/10.1038/sj.bjc.6604629 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Kalikaki, A
Koutsopoulos, A
Trypaki, M
Souglakos, J
Stathopoulos, E
Georgoulias, V
Mavroudis, D
Voutsina, A
Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC
title Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC
title_full Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC
title_fullStr Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC
title_full_unstemmed Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC
title_short Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC
title_sort comparison of egfr and k-ras gene status between primary tumours and corresponding metastases in nsclc
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538768/
https://www.ncbi.nlm.nih.gov/pubmed/19238633
http://dx.doi.org/10.1038/sj.bjc.6604629
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