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ID

45562

Description

Principal Investigator: Adolfo Ferrando, Institute for Cancer Genetics, Columbia University, New York, NY, USA MeSH: Lymphoma, T-Cell, Peripheral,Lymphoma, Non-Hodgkin https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000689 Peripheral T-cell lymphomas (PTCLs) are a heterogeneous and poorly understood group of non Hodgkin lymphomas. We aim to identify new genetic alterations in PTCL transformation by using a combination of whole exome sequencing of tumor-normal DNA pairs, RNAseq analysis and targeted deep sequencing of candidate genes. Our data identified highly recurrent mutations in epigenetic factors such as TET2, DNMT3A and IDH2 as well as a new highly prevalent mutation in RHOA, the G17V allele that is present in almost 70% of angioimmunoblastic T-cell lymphomas (AITL) and almost 20% of not otherwise specified PTCL (PTCL NOS) samples. In addition, we describe new and recurrent genetic defects including mutations in FYN, ATM, B2M and CD58 implicating SRC signaling, impaired DNA damage response and escape from immune surveillance processes as key players in the pathogenesis of PTCL.

Lien

dbGaP-study=phs000689

Mots-clés

  1. 13/01/2023 13/01/2023 - Chiara Middel
Détendeur de droits

Adolfo Ferrando, Institute for Cancer Genetics, Columbia University, New York, NY, USA

Téléchargé le

13 janvier 2023

DOI

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Licence

Creative Commons BY 4.0

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    dbGaP phs000689 Genomic Analysis of Peripheral T-Cell Lymphomas

    Eligibility Criteria

    Inclusion and exclusion criteria
    Description

    Inclusion and exclusion criteria

    Alias
    UMLS CUI [1,1]
    C1512693 (Inclusion)
    UMLS CUI [1,2]
    C0680251 (Exclusion Criteria)
    De novo diagnoses of peripheral T-cell lymphoma
    Description

    Elig.phs000689.v1.p1.1

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1515568 (de novo)
    UMLS CUI [1,2]
    C0011900 (Diagnosis)
    SNOMED
    439401001
    LOINC
    LP30831-9
    UMLS CUI [1,3]
    C0079774 (Peripheral T-Cell Lymphoma)
    SNOMED
    3172003
    Matched tumor and normal genomic DNA (for exome sequencing only)
    Description

    Elig.phs000689.v1.p1.2

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0150103 (MATCHING)
    UMLS CUI [1,2]
    C4331441 (Tumor DNA)
    UMLS CUI [1,3]
    C3272453 (Genomic DNA)

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