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Clinical Significance of Somatic Mutations in RAS/RAF/MAPK Signaling Pathway in Moroccan and North African Colorectal Cancer Patients

BACKGROUND: Mutations in RAS (KRAS, NRAS) and BRAF genes are the main biomarker predicting response to anti-EGFR monoclonal antibodies in targeted therapy in colorectal cancer (CRC). OBJECTIVE: Our study aims to evaluate the frequencies of KRAS, NRAS and BRAF mutations and their possible association...

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Autores principales: Benmokhtar, Soukaina, Laraqui, Abdelilah, El Boukhrissi, Fatima, Hilali, Farida, Bajjou, Tahar, Jafari, Meryem, Elzaitouni, Sara, Baba, Walid, El Mchichi, Bouchra, Elannaz, Hicham, Lahlou, Idriss Amine, Chahdi, Hafsa, Oukabli, Mohamed, Mahfoud, Tarik, Tanz, Rachid, Ichou, Mohamed, Ennibi, Khaled, Dakka, Nadia, Sekhsokh, Yassine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930961/
https://www.ncbi.nlm.nih.gov/pubmed/36444585
http://dx.doi.org/10.31557/APJCP.2022.23.11.3725
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author Benmokhtar, Soukaina
Laraqui, Abdelilah
El Boukhrissi, Fatima
Hilali, Farida
Bajjou, Tahar
Jafari, Meryem
Elzaitouni, Sara
Baba, Walid
El Mchichi, Bouchra
Elannaz, Hicham
Lahlou, Idriss Amine
Chahdi, Hafsa
Oukabli, Mohamed
Mahfoud, Tarik
Tanz, Rachid
Ichou, Mohamed
Ennibi, Khaled
Dakka, Nadia
Sekhsokh, Yassine
author_facet Benmokhtar, Soukaina
Laraqui, Abdelilah
El Boukhrissi, Fatima
Hilali, Farida
Bajjou, Tahar
Jafari, Meryem
Elzaitouni, Sara
Baba, Walid
El Mchichi, Bouchra
Elannaz, Hicham
Lahlou, Idriss Amine
Chahdi, Hafsa
Oukabli, Mohamed
Mahfoud, Tarik
Tanz, Rachid
Ichou, Mohamed
Ennibi, Khaled
Dakka, Nadia
Sekhsokh, Yassine
author_sort Benmokhtar, Soukaina
collection PubMed
description BACKGROUND: Mutations in RAS (KRAS, NRAS) and BRAF genes are the main biomarker predicting response to anti-EGFR monoclonal antibodies in targeted therapy in colorectal cancer (CRC). OBJECTIVE: Our study aims to evaluate the frequencies of KRAS, NRAS and BRAF mutations and their possible associations with clinico-pathological features in CRC patients from Morocco. METHODS: DNA was extracted from 80 FFPE samples using the QIAamp DNA FFPE-kit. RAS and BRAF mutations were assessed by pyrosequencing assays using Qiagen, KRAS Pyro®kit 24.V1, Ras-Extension Pyro®kit 24.V1 and BRAF Pyro®Kit 24.V1, respectively, and carried out in the PyroMark-Q24. RESULTS: RAS mutations were identified in 57.5% (56.2% in KRAS, 8.8% in NRAS). In KRAS gene, exon 2 mutations accounted for 93.3% (68.9% in codon 12, 24.4% in codon 13). Within codon 12, G12D was the most prevalent mutation (37.7%), followed by G12C (13.4%), G12S (8.9%) and G12V (6.6%). Within codon 13, the most frequently observed mutation was G13D (22.3%). The mutation rates of exon 3 and 4 were 15.6% and 13.3%, respectively. In exon 3 codon 61, 2.3% patients were detected with two concurrent mutations (Q61R, Q61H), and 4.4% with three concurrent mutations (Q61R, Q61H, Q61L). In NRAS gene, the mutation rates of exon 2, 3 and 4 were 57.1%, 28.6%, and 14.3%, respectively. G13A and Q61H were the most common mutations, accounting for 42.9% and 28.5%, respectively. There were 13% patients with concurrent KRAS/NRAS mutation and 4.3% wt KRAS with NRAS mutations. No mutations were identified in BRAF gene. In both sexes, KRAS codon 12 mutations were associated with higher stage III/IV tumors. Moreover, Patients whose tumor is in the proximal colon (56.3%) are more likely to harbor KRAS mutations than those tumor located in rectum (25%). CONCLUSION: RAS mutations could be useful in future target anti-EGFR therapy and molecular CRC screening strategy in Morocco.
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spelling pubmed-99309612023-02-16 Clinical Significance of Somatic Mutations in RAS/RAF/MAPK Signaling Pathway in Moroccan and North African Colorectal Cancer Patients Benmokhtar, Soukaina Laraqui, Abdelilah El Boukhrissi, Fatima Hilali, Farida Bajjou, Tahar Jafari, Meryem Elzaitouni, Sara Baba, Walid El Mchichi, Bouchra Elannaz, Hicham Lahlou, Idriss Amine Chahdi, Hafsa Oukabli, Mohamed Mahfoud, Tarik Tanz, Rachid Ichou, Mohamed Ennibi, Khaled Dakka, Nadia Sekhsokh, Yassine Asian Pac J Cancer Prev Research Article BACKGROUND: Mutations in RAS (KRAS, NRAS) and BRAF genes are the main biomarker predicting response to anti-EGFR monoclonal antibodies in targeted therapy in colorectal cancer (CRC). OBJECTIVE: Our study aims to evaluate the frequencies of KRAS, NRAS and BRAF mutations and their possible associations with clinico-pathological features in CRC patients from Morocco. METHODS: DNA was extracted from 80 FFPE samples using the QIAamp DNA FFPE-kit. RAS and BRAF mutations were assessed by pyrosequencing assays using Qiagen, KRAS Pyro®kit 24.V1, Ras-Extension Pyro®kit 24.V1 and BRAF Pyro®Kit 24.V1, respectively, and carried out in the PyroMark-Q24. RESULTS: RAS mutations were identified in 57.5% (56.2% in KRAS, 8.8% in NRAS). In KRAS gene, exon 2 mutations accounted for 93.3% (68.9% in codon 12, 24.4% in codon 13). Within codon 12, G12D was the most prevalent mutation (37.7%), followed by G12C (13.4%), G12S (8.9%) and G12V (6.6%). Within codon 13, the most frequently observed mutation was G13D (22.3%). The mutation rates of exon 3 and 4 were 15.6% and 13.3%, respectively. In exon 3 codon 61, 2.3% patients were detected with two concurrent mutations (Q61R, Q61H), and 4.4% with three concurrent mutations (Q61R, Q61H, Q61L). In NRAS gene, the mutation rates of exon 2, 3 and 4 were 57.1%, 28.6%, and 14.3%, respectively. G13A and Q61H were the most common mutations, accounting for 42.9% and 28.5%, respectively. There were 13% patients with concurrent KRAS/NRAS mutation and 4.3% wt KRAS with NRAS mutations. No mutations were identified in BRAF gene. In both sexes, KRAS codon 12 mutations were associated with higher stage III/IV tumors. Moreover, Patients whose tumor is in the proximal colon (56.3%) are more likely to harbor KRAS mutations than those tumor located in rectum (25%). CONCLUSION: RAS mutations could be useful in future target anti-EGFR therapy and molecular CRC screening strategy in Morocco. West Asia Organization for Cancer Prevention 2022-11 /pmc/articles/PMC9930961/ /pubmed/36444585 http://dx.doi.org/10.31557/APJCP.2022.23.11.3725 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License. https://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Research Article
Benmokhtar, Soukaina
Laraqui, Abdelilah
El Boukhrissi, Fatima
Hilali, Farida
Bajjou, Tahar
Jafari, Meryem
Elzaitouni, Sara
Baba, Walid
El Mchichi, Bouchra
Elannaz, Hicham
Lahlou, Idriss Amine
Chahdi, Hafsa
Oukabli, Mohamed
Mahfoud, Tarik
Tanz, Rachid
Ichou, Mohamed
Ennibi, Khaled
Dakka, Nadia
Sekhsokh, Yassine
Clinical Significance of Somatic Mutations in RAS/RAF/MAPK Signaling Pathway in Moroccan and North African Colorectal Cancer Patients
title Clinical Significance of Somatic Mutations in RAS/RAF/MAPK Signaling Pathway in Moroccan and North African Colorectal Cancer Patients
title_full Clinical Significance of Somatic Mutations in RAS/RAF/MAPK Signaling Pathway in Moroccan and North African Colorectal Cancer Patients
title_fullStr Clinical Significance of Somatic Mutations in RAS/RAF/MAPK Signaling Pathway in Moroccan and North African Colorectal Cancer Patients
title_full_unstemmed Clinical Significance of Somatic Mutations in RAS/RAF/MAPK Signaling Pathway in Moroccan and North African Colorectal Cancer Patients
title_short Clinical Significance of Somatic Mutations in RAS/RAF/MAPK Signaling Pathway in Moroccan and North African Colorectal Cancer Patients
title_sort clinical significance of somatic mutations in ras/raf/mapk signaling pathway in moroccan and north african colorectal cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930961/
https://www.ncbi.nlm.nih.gov/pubmed/36444585
http://dx.doi.org/10.31557/APJCP.2022.23.11.3725
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