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DOI 10.31557/apjcp.2022.23.11.3725

Медицинская библиотека · Asian Pacific journal of cancer prevention : APJCP · 2022

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, El Zaitouni 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

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Аннотация

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.

Для цитирования: Benmokhtar Soukaina, Laraqui Abdelilah, El Boukhrissi Fatima, Hilali Farida, Bajjou Tahar, Jafari Meryem, El Zaitouni 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.. Asian Pacific journal of cancer prevention : APJCP. 2022. DOI: 10.31557/apjcp.2022.23.11.3725.

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