ID

45195

Description

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.

Lien

dbGaP study = phs000370

Mots-clés

  1. 19/08/2022 19/08/2022 - Simon Heim
  2. 12/10/2022 12/10/2022 - Adrian Schulz
Détendeur de droits

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

Téléchargé le

12 octobre 2022

DOI

Pour une demande vous connecter.

Licence

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
Description

pht002382

Subject ID
Description

SUBJID

Type de données

string

Alias
UMLS CUI [1,1]
C2348585
Sample ID
Description

SAMPID

Type de données

string

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

SAMPLE_USE

Type de données

text

Alias
UMLS CUI [1,1]
C1524063
UMLS CUI [1,2]
C0370003

Similar models

pht002382.v2.p1

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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