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    Subjects/Pathology/Carcinogenesis and Oncogenes
    Carcinogenesis and Oncogenes
    easy
    microscope Pathology

    The RAS gene is mutated in approximately what percentage of human cancers, making it the most frequently altered oncogene?

    A. 30–50%
    B. 60–70%
    C. 10–15%
    D. 80–90%

    Explanation

    RAS Oncogene Prevalence in Cancer

    Key Point
    RAS mutations are the single most common oncogenic alteration across all human malignancies, found in approximately 30–50% of cancers globally.
    RAS Mutation Frequency by Cancer Type
    Table
    Cancer TypeRAS Mutation FrequencyNotes
    Pancreatic adenocarcinoma75–90%Highest frequency
    Colorectal cancer40–50%Common in adenomas
    Lung cancer (NSCLC)20–30%Especially adenocarcinoma
    Melanoma15–25%Varies by subtype
    Acute myeloid leukemia20–30%FLT3 and NPM1 also common
    Thyroid cancer20–40%Papillary and follicular types
    High-YieldNEET PG
    The 30–50% figure is a testable fact in NEET PG. RAS is the most frequently mutated oncogene, followed by TP53 (most frequently mutated tumor suppressor).
    Why RAS Is So Commonly Mutated
    1. 1.
      Three isoforms — KRAS, NRAS, HRAS provide redundancy; mutation of any one can drive cancer
    2. 2.
      Single amino acid substitution — Point mutations at codons 12, 13, or 61 cause constitutive GTPase activity
    3. 3.
      Early event — RAS mutations often occur early in carcinogenesis, especially in colorectal adenoma-carcinoma sequence
    4. 4.
      Broad tissue distribution — RAS is expressed in nearly all cell types
    Mnemonic
    RAS = Remarkably Altered in ~50% of cancers (remember the 30–50% range).

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