0 Avaliações

ID

45473

Descrição

Principal Investigator: Laura Pasqualucci, MD, Institute for Cancer Genetics, Columbia University, New York, NY, USA MeSH: Lymphoma, Non-Hodgkin,Lymphoma, B-Cell https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000502 Splenic Marginal Zone Lymphoma (SMZL) is a B-cell malignancy of unknown pathogenesis and thus orphan of targeted therapies. By integrating whole-exome sequencing and copy-number analysis of 8 paired tumor-normal DNAs from patients with SMZL, we show that the typical SMZL exome carries ~30 genetic alterations. Targeted resequencing of selected candidates in an extended panel of 40-117 samples revealed activating mutations of NOTCH2, a gene required for marginal-zone (MZ) development, as the most frequent and SMZL-specific lesion, accounting for approximately 20% of cases. Additional altered genes suggest that deregulation of signaling pathways normally involved in MZ development (NOTCH, NF-kappa B, and B-cell receptor) represents a critical event in SMZL pathogenesis. These findings have direct implications for the treatment of SMZL patients since drugs are available which can target NOTCH as well as other pathways deregulated in this disease.

Link

dbGap study = phs000502

Palavras-chave

  1. 31/10/2022 31/10/2022 - Tabea Kampen
  2. 13/12/2022 13/12/2022 - Kristina Keller
Titular dos direitos

Laura Pasqualucci, MD, Institute for Cancer Genetics, Columbia University, New York, NY, USA

Transferido a

13 de dezembro de 2022

DOI

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Licença

Creative Commons BY 4.0

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    dbGaP phs000502 Genome-Wide Analysis of Splenic Marginal Zone Lymphoma

    Sample ID, subject ID and sample use variables obtained from participants with splenic marginal zone lymphoma and involved in the "Genome-Wide Analysis of Splenic Marginal Zone Lymphoma" project.

    pht002814
    Descrição

    pht002814

    De-identified subject's ID
    Descrição

    SUBJID

    Tipo de dados

    string

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

    SAMPID

    Tipo de dados

    string

    Alias
    UMLS CUI [1,1]
    C1299222
    Sample use. SNP_Array: SNP genotypes obtained using standard or custom microarrays; WES_SRA: Whole exome sequencing data available through SRA
    Descrição

    SAMPLE_USE

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0200345
    UMLS CUI [1,2]
    C1524063
    UMLS CUI [2,1]
    C3897601
    UMLS CUI [3,1]
    C3640077
    UMLS CUI [3,2]
    C3506382

    Similar models

    Sample ID, subject ID and sample use variables obtained from participants with splenic marginal zone lymphoma and involved in the "Genome-Wide Analysis of Splenic Marginal Zone Lymphoma" project.

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    pht002814
    SUBJID
    Item
    De-identified subject's ID
    string
    C2348585 (UMLS CUI [1,1])
    SAMPID
    Item
    Sample ID
    string
    C1299222 (UMLS CUI [1,1])
    SAMPLE_USE
    Item
    Sample use. SNP_Array: SNP genotypes obtained using standard or custom microarrays; WES_SRA: Whole exome sequencing data available through SRA
    text
    C0200345 (UMLS CUI [1,1])
    C1524063 (UMLS CUI [1,2])
    C3897601 (UMLS CUI [2,1])
    C3640077 (UMLS CUI [3,1])
    C3506382 (UMLS CUI [3,2])

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