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High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer

BACKGROUND: KRAS is an EGFR effector in the RAS/RAF/ERK cascade that is mutated in about 40% of metastatic colorectal cancer (mCRC). Activating mutations in codons 12 and 13 of the KRAS gene are the only established negative predictors of response to anti-EGFR therapy and patients whose tumors harbo...

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Autores principales: Guedes, Joana G, Veiga, Isabel, Rocha, Patrícia, Pinto, Pedro, Pinto, Carla, Pinheiro, Manuela, Peixoto, Ana, Fragoso, Maria, Raimundo, Ana, Ferreira, Paula, Machado, Manuela, Sousa, Nuno, Lopes, Paula, Araújo, António, Macedo, Joana, Alves, Fernando, Coutinho, Camila, Henrique, Rui, Santos, Lúcio L, Teixeira, Manuel R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623853/
https://www.ncbi.nlm.nih.gov/pubmed/23548132
http://dx.doi.org/10.1186/1471-2407-13-169
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author Guedes, Joana G
Veiga, Isabel
Rocha, Patrícia
Pinto, Pedro
Pinto, Carla
Pinheiro, Manuela
Peixoto, Ana
Fragoso, Maria
Raimundo, Ana
Ferreira, Paula
Machado, Manuela
Sousa, Nuno
Lopes, Paula
Araújo, António
Macedo, Joana
Alves, Fernando
Coutinho, Camila
Henrique, Rui
Santos, Lúcio L
Teixeira, Manuel R
author_facet Guedes, Joana G
Veiga, Isabel
Rocha, Patrícia
Pinto, Pedro
Pinto, Carla
Pinheiro, Manuela
Peixoto, Ana
Fragoso, Maria
Raimundo, Ana
Ferreira, Paula
Machado, Manuela
Sousa, Nuno
Lopes, Paula
Araújo, António
Macedo, Joana
Alves, Fernando
Coutinho, Camila
Henrique, Rui
Santos, Lúcio L
Teixeira, Manuel R
author_sort Guedes, Joana G
collection PubMed
description BACKGROUND: KRAS is an EGFR effector in the RAS/RAF/ERK cascade that is mutated in about 40% of metastatic colorectal cancer (mCRC). Activating mutations in codons 12 and 13 of the KRAS gene are the only established negative predictors of response to anti-EGFR therapy and patients whose tumors harbor such mutations are not candidates for therapy. However, 40 to 60% of wild-type cases do not respond to anti-EGFR therapy, suggesting the involvement of other genes that act downstream of EGFR in the RAS-RAF-MAPK and PI3K-AKT pathways or activating KRAS mutations at other locations of the gene. METHODS: DNA was obtained from a consecutive series of 201 mCRC cases (FFPE tissue), wild-type for KRAS exon 2 (codons 12 and 13). Mutational analysis of KRAS (exons 3 and 4), BRAF (exons 11 and 15), and PIK3CA (exons 9 and 20) was performed by high resolution melting (HRM) and positive cases were then sequenced. RESULTS: One mutation was present in 23.4% (47/201) of the cases and 3.0% additional cases (6/201) had two concomitant mutations. A total of 53 cases showed 59 mutations, with the following distribution: 44.1% (26/59) in KRAS (13 in exon 3 and 13 in exon 4), 18.6% (11/59) in BRAF (two in exon 11 and nine in exon 15) and 37.3% (22/59) in PIK3CA (16 in exon 9 and six in exon 20). In total, 26.4% (53/201) of the cases had at least one mutation and the remaining 73.6% (148/201) were wild-type for all regions studied. Five of the mutations we report, four in KRAS and one in BRAF, have not previously been described in CRC. BRAF and PIK3CA mutations were more frequent in the colon than in the sigmoid or rectum: 20.8% vs. 1.6% vs. 0.0% (P=0.000) for BRAF and 23.4% vs. 12.1% vs. 5.4% (P=0.011) for PIK3CA mutations. CONCLUSIONS: About one fourth of mCRC cases wild-type for KRAS codons 12 and 13 present other mutations either in KRAS, BRAF, or PIK3CA, many of which may explain the lack of response to anti-EGFR therapy observed in a significant proportion of these patients.
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spelling pubmed-36238532013-04-12 High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer Guedes, Joana G Veiga, Isabel Rocha, Patrícia Pinto, Pedro Pinto, Carla Pinheiro, Manuela Peixoto, Ana Fragoso, Maria Raimundo, Ana Ferreira, Paula Machado, Manuela Sousa, Nuno Lopes, Paula Araújo, António Macedo, Joana Alves, Fernando Coutinho, Camila Henrique, Rui Santos, Lúcio L Teixeira, Manuel R BMC Cancer Research Article BACKGROUND: KRAS is an EGFR effector in the RAS/RAF/ERK cascade that is mutated in about 40% of metastatic colorectal cancer (mCRC). Activating mutations in codons 12 and 13 of the KRAS gene are the only established negative predictors of response to anti-EGFR therapy and patients whose tumors harbor such mutations are not candidates for therapy. However, 40 to 60% of wild-type cases do not respond to anti-EGFR therapy, suggesting the involvement of other genes that act downstream of EGFR in the RAS-RAF-MAPK and PI3K-AKT pathways or activating KRAS mutations at other locations of the gene. METHODS: DNA was obtained from a consecutive series of 201 mCRC cases (FFPE tissue), wild-type for KRAS exon 2 (codons 12 and 13). Mutational analysis of KRAS (exons 3 and 4), BRAF (exons 11 and 15), and PIK3CA (exons 9 and 20) was performed by high resolution melting (HRM) and positive cases were then sequenced. RESULTS: One mutation was present in 23.4% (47/201) of the cases and 3.0% additional cases (6/201) had two concomitant mutations. A total of 53 cases showed 59 mutations, with the following distribution: 44.1% (26/59) in KRAS (13 in exon 3 and 13 in exon 4), 18.6% (11/59) in BRAF (two in exon 11 and nine in exon 15) and 37.3% (22/59) in PIK3CA (16 in exon 9 and six in exon 20). In total, 26.4% (53/201) of the cases had at least one mutation and the remaining 73.6% (148/201) were wild-type for all regions studied. Five of the mutations we report, four in KRAS and one in BRAF, have not previously been described in CRC. BRAF and PIK3CA mutations were more frequent in the colon than in the sigmoid or rectum: 20.8% vs. 1.6% vs. 0.0% (P=0.000) for BRAF and 23.4% vs. 12.1% vs. 5.4% (P=0.011) for PIK3CA mutations. CONCLUSIONS: About one fourth of mCRC cases wild-type for KRAS codons 12 and 13 present other mutations either in KRAS, BRAF, or PIK3CA, many of which may explain the lack of response to anti-EGFR therapy observed in a significant proportion of these patients. BioMed Central 2013-04-01 /pmc/articles/PMC3623853/ /pubmed/23548132 http://dx.doi.org/10.1186/1471-2407-13-169 Text en Copyright © 2013 Guedes et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Guedes, Joana G
Veiga, Isabel
Rocha, Patrícia
Pinto, Pedro
Pinto, Carla
Pinheiro, Manuela
Peixoto, Ana
Fragoso, Maria
Raimundo, Ana
Ferreira, Paula
Machado, Manuela
Sousa, Nuno
Lopes, Paula
Araújo, António
Macedo, Joana
Alves, Fernando
Coutinho, Camila
Henrique, Rui
Santos, Lúcio L
Teixeira, Manuel R
High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer
title High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer
title_full High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer
title_fullStr High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer
title_full_unstemmed High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer
title_short High resolution melting analysis of KRAS, BRAF and PIK3CA in KRAS exon 2 wild-type metastatic colorectal cancer
title_sort high resolution melting analysis of kras, braf and pik3ca in kras exon 2 wild-type metastatic colorectal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623853/
https://www.ncbi.nlm.nih.gov/pubmed/23548132
http://dx.doi.org/10.1186/1471-2407-13-169
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