Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784889143126392832 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9930961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | West Asia Organization for Cancer Prevention |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT benmokhtarsoukaina clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT laraquiabdelilah clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT elboukhrissifatima clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT hilalifarida clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT bajjoutahar clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT jafarimeryem clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT elzaitounisara clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT babawalid clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT elmchichibouchra clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT elannazhicham clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT lahlouidrissamine clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT chahdihafsa clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT oukablimohamed clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT mahfoudtarik clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT tanzrachid clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT ichoumohamed clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT ennibikhaled clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT dakkanadia clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients AT sekhsokhyassine clinicalsignificanceofsomaticmutationsinrasrafmapksignalingpathwayinmoroccanandnorthafricancolorectalcancerpatients |