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ID

45195

Descrição

Principal Investigator: Todd Golub, Broad Institute, Cambridge, MA and Dana Farber Cancer Institute, Boston, MA, USA MeSH: Head and Neck Neoplasms https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000370 This study was the first-known large-scale effort to uncover the mutational spectrum of head and neck cancers. We analyzed whole-exome sequence from 92 tumor-normal pairs and retained 74 of them for significance analysis. The majority exhibited a mutational profile consistent with tobacco exposure; human papilloma virus sequence was detectable in 15% of cases. In addition to identifying previously known HNSCC genes (*TP53, CDKN2A, PTEN, PIK3CA, and HRAS*), the analysis revealed many genes not previously implicated in this malignancy. At least 30% of cases harbor mutations in genes (such as *NOTCH1, IRF6, TP63*) that regulate squamous differentiation, implicating alterations in this process as a major driver of HNSCC carcinogenesis. Altogether, the results suggest that large-scale exome sequencing may illuminate fundamental tumorigenic mechanisms with important therapeutic implications.

Link

dbGaP study = phs000370

Palavras-chave

  1. 8/19/22 8/19/22 - Simon Heim
  2. 10/12/22 10/12/22 - Adrian Schulz
Titular dos direitos

Todd Golub, Broad Institute, Cambridge, MA and Dana Farber Cancer Institute, Boston, MA, USA

Transferido a

October 12, 2022

DOI

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Licença

Creative Commons BY 4.0

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    dbGaP phs000370 The Mutational Landscape of Head and Neck Squamous Cell Carcinoma

    pht002382.v2.p1

    pht002382
    Descrição

    pht002382

    Subject ID
    Descrição

    SUBJID

    Tipo de dados

    string

    Alias
    UMLS CUI [1,1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Sample ID
    Descrição

    SAMPID

    Tipo de dados

    string

    Alias
    UMLS CUI [1,1]
    C1299222 (Sample identification number)
    SNOMED
    372274003
    Sample use. WES_SRA: Whole exome sequencing; individual_MAF: Whole genome or partial SNP genotypes are reported in mutation annotation file (.maf) format
    Descrição

    SAMPLE_USE

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C1524063 (Use of)
    SNOMED
    260676000
    UMLS CUI [1,2]
    C0370003 (Specimen)
    SNOMED
    123038009
    LOINC
    LP7593-9

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    pht002382.v2.p1

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    pht002382
    SUBJID
    Item
    Subject ID
    string
    C2348585 (UMLS CUI [1,1])
    SAMPID
    Item
    Sample ID
    string
    C1299222 (UMLS CUI [1,1])
    SAMPLE_USE
    Item
    Sample use. WES_SRA: Whole exome sequencing; individual_MAF: Whole genome or partial SNP genotypes are reported in mutation annotation file (.maf) format
    text
    C1524063 (UMLS CUI [1,1])
    C0370003 (UMLS CUI [1,2])

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