0 Evaluaciones

ID

45473

Descripción

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

Palabras clave

  1. 31.10.22 31.10.22 - Tabea Kampen
  2. 13.12.22 13.12.22 - Kristina Keller
Titular de derechos de autor

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

Subido en

13. Dezember 2022

DOI

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Licencia

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
    Descripción

    pht002814

    De-identified subject's ID
    Descripción

    SUBJID

    Tipo de datos

    string

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

    SAMPID

    Tipo de datos

    string

    Alias
    UMLS CUI [1,1]
    C1299222 (Sample identification number)
    SNOMED
    372274003
    Sample use. SNP_Array: SNP genotypes obtained using standard or custom microarrays; WES_SRA: Whole exome sequencing data available through SRA
    Descripción

    SAMPLE_USE

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0200345 (Specimen Collection)
    SNOMED
    17636008
    UMLS CUI [1,2]
    C1524063 (Use of)
    SNOMED
    260676000
    UMLS CUI [2,1]
    C3897601 (Single Nucleotide Polymorphism Array)
    UMLS CUI [3,1]
    C3640077 (Whole Exome Sequencing)
    UMLS CUI [3,2]
    C3506382 (platelet associated serotonin release assay (SRA))

    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 datos
    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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