Evidence map›Paper›PMID 42063916›Full record

ArticleAfrican health sciences2026

Differences in anatomoclinical profiles between RAS-Mutated and Wild-Type colorectal cancers in an Eastern Algerian Cohort.

Yahia Massinissa, Afaf Benhouda, Hachani Khadraoui, Djahida Benouda, Wafa Khettache, Atika Soussi

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Article in African health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yahia MassinissaBiotechnology's Laboratory of the Bioactive Molecules and the Cellular Physiopathology, Faculty of Biological Sciences, Department of Biology and Living Organisms, University of Mustapha Ben Boulaid. 53 Constantine Rd, Fésdis, Batna 05078, Algeria. Tel: +213-676- 002083.
Afaf BenhoudaBiotechnology's Laboratory of the Bioactive Molecules and the Cellular Physiopathology, Faculty of Biological Sciences, Department of Biology and Living Organisms, University of Mustapha Ben Boulaid. 53 Constantine Rd, Fésdis, Batna 05078, Algeria. Tel: +213-676- 002083.
Hachani KhadraouiLaboratory of Anapathology, CHU of Batna, Algeria.
Djahida BenoudaBiotechnology's Laboratory of the Bioactive Molecules and the Cellular Physiopathology, Faculty of Biological Sciences, Department of Biology and Living Organisms, University of Mustapha Ben Boulaid. 53 Constantine Rd, Fésdis, Batna 05078, Algeria. Tel: +213-676- 002083.
Wafa KhettacheBiotechnology's Laboratory of the Bioactive Molecules and the Cellular Physiopathology, Faculty of Biological Sciences, Department of Biology and Living Organisms, University of Mustapha Ben Boulaid. 53 Constantine Rd, Fésdis, Batna 05078, Algeria. Tel: +213-676- 002083.
Atika SoussiBiotechnology's Laboratory of the Bioactive Molecules and the Cellular Physiopathology, Faculty of Biological Sciences, Department of Biology and Living Organisms, University of Mustapha Ben Boulaid. 53 Constantine Rd, Fésdis, Batna 05078, Algeria. Tel: +213-676- 002083.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colorectal cancer (CRC) ranks as the third most prevalent malignancy globally, with incidence rates rising steadily in Algeria. Prognostic assessment of CRC increasingly relies on molecular profiling, particularly mutations in the KRAS gene a critical determinant of resistance to anti-EGFR therapies in metastatic disease. Objectives: This study investigates the KRAS mutational spectrum and its association with clinicopathological features in CRC patients from Batna, Eastern Algeria. Methods: In a retrospective analysis of 91 cases, KRAS mutations were identified in 46.2% of tumors (wild-type: 58.3%) using RT-PCR and sequencing. Results: The most frequent alterations localized to codons 12 and 13 (exons 1-2), with p.G12D (c.35G>A) and p.G13D (c.38G>A) predominating. Strikingly, KRAS mutation status showed no significant correlation with age, sex, tumor size, histology, metastatic pattern, or TNM stage suggesting its role as an independent molecular driver rather than a surrogate for conventional prognostic markers. Conclusion: These findings underscore the high prevalence of KRAS mutations in Algerian CRC patients and highlight their potential utility in refining therapeutic strategies, particularly for anti-EGFR eligibility. The study provides the first regional dataset from Eastern Algeria, addressing a critical gap in North African oncogenomics.

Indexed as

Colorectal NeoplasmsMutationProto-Oncogene Proteins p21(ras)AdultAgedAlgeriaDNA Mutational AnalysisFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesKRAS protein, humanProto-Oncogene Proteins p21(ras)AlgeriaCCRmutated KRASmutationswild-type KRAS

Identifiers

PMID42063916
PMCPMC13126134

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