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KRAS and BRAF mutational status in colon cancer from Albanian patients

BACKGROUND: Numerous clinical studies have shown that anti-EGFR therapies are effective only in a subset of patients with colorectal cancer. Mutations in the KRAS and BRAF genes have been confirmed as negative predictors of the response to EGFR-targeted therapies. In this study we evaluated KRAS and...

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Autores principales: Martinetti, Daniela, Costanzo, Rosario, Kadare, Shahin, Alimehmeti, Mehdiu, Colarossi, Cristina, Canzonieri, Vincenzo, Berretta, Massimiliano, Memeo, Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198623/
https://www.ncbi.nlm.nih.gov/pubmed/25267307
http://dx.doi.org/10.1186/s13000-014-0187-7
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author Martinetti, Daniela
Costanzo, Rosario
Kadare, Shahin
Alimehmeti, Mehdiu
Colarossi, Cristina
Canzonieri, Vincenzo
Berretta, Massimiliano
Memeo, Lorenzo
author_facet Martinetti, Daniela
Costanzo, Rosario
Kadare, Shahin
Alimehmeti, Mehdiu
Colarossi, Cristina
Canzonieri, Vincenzo
Berretta, Massimiliano
Memeo, Lorenzo
author_sort Martinetti, Daniela
collection PubMed
description BACKGROUND: Numerous clinical studies have shown that anti-EGFR therapies are effective only in a subset of patients with colorectal cancer. Mutations in the KRAS and BRAF genes have been confirmed as negative predictors of the response to EGFR-targeted therapies. In this study we evaluated KRAS and BRAF status in 159 colorectal cancer samples obtained from the University of Tirana. METHODS: We evaluated KRAS mutations in codons 12, 13, 61, 146 and in codon 600 of BRAF by direct sequencing. 90 patients were male (57%) and 69 female (43%); the patients’ ages ranged from 17 to 85 (median 61.7). 24 patient were stage I, 36 stage II, 84 stage III and 15 stage IV. RESULTS: Out of the 159 cases, 28 (17,6%) showed KRAS mutation (13 G12D, 4 G12C, 4 G12V, 3 G12A, 2 G13 D, 1 G12S and 1 A146T), and 10 (6,3%) showed BRAF mutation (all V600E). No significant correlations between KRAS and BRAF mutations and various clinicopathological parameters was found. This is the first report of KRAS and BRAF status in Albanian patients with colorectal carcinoma (CRC) and though the relatively small sample size might not provide enough statistics power. CONCLUSIONS: The results of KRAS and BRAF mutation analysis could be used in the selection of patients for anti-EGFR therapy. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_187
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spelling pubmed-41986232014-10-17 KRAS and BRAF mutational status in colon cancer from Albanian patients Martinetti, Daniela Costanzo, Rosario Kadare, Shahin Alimehmeti, Mehdiu Colarossi, Cristina Canzonieri, Vincenzo Berretta, Massimiliano Memeo, Lorenzo Diagn Pathol Research BACKGROUND: Numerous clinical studies have shown that anti-EGFR therapies are effective only in a subset of patients with colorectal cancer. Mutations in the KRAS and BRAF genes have been confirmed as negative predictors of the response to EGFR-targeted therapies. In this study we evaluated KRAS and BRAF status in 159 colorectal cancer samples obtained from the University of Tirana. METHODS: We evaluated KRAS mutations in codons 12, 13, 61, 146 and in codon 600 of BRAF by direct sequencing. 90 patients were male (57%) and 69 female (43%); the patients’ ages ranged from 17 to 85 (median 61.7). 24 patient were stage I, 36 stage II, 84 stage III and 15 stage IV. RESULTS: Out of the 159 cases, 28 (17,6%) showed KRAS mutation (13 G12D, 4 G12C, 4 G12V, 3 G12A, 2 G13 D, 1 G12S and 1 A146T), and 10 (6,3%) showed BRAF mutation (all V600E). No significant correlations between KRAS and BRAF mutations and various clinicopathological parameters was found. This is the first report of KRAS and BRAF status in Albanian patients with colorectal carcinoma (CRC) and though the relatively small sample size might not provide enough statistics power. CONCLUSIONS: The results of KRAS and BRAF mutation analysis could be used in the selection of patients for anti-EGFR therapy. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_187 BioMed Central 2014-09-30 /pmc/articles/PMC4198623/ /pubmed/25267307 http://dx.doi.org/10.1186/s13000-014-0187-7 Text en © Martinetti et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Martinetti, Daniela
Costanzo, Rosario
Kadare, Shahin
Alimehmeti, Mehdiu
Colarossi, Cristina
Canzonieri, Vincenzo
Berretta, Massimiliano
Memeo, Lorenzo
KRAS and BRAF mutational status in colon cancer from Albanian patients
title KRAS and BRAF mutational status in colon cancer from Albanian patients
title_full KRAS and BRAF mutational status in colon cancer from Albanian patients
title_fullStr KRAS and BRAF mutational status in colon cancer from Albanian patients
title_full_unstemmed KRAS and BRAF mutational status in colon cancer from Albanian patients
title_short KRAS and BRAF mutational status in colon cancer from Albanian patients
title_sort kras and braf mutational status in colon cancer from albanian patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198623/
https://www.ncbi.nlm.nih.gov/pubmed/25267307
http://dx.doi.org/10.1186/s13000-014-0187-7
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