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Following a change to our organizational structure effective April 1, 2026, this division has been renamed from the "Database Center for Life Science, Joint Support-Center for Data Science Research" to the "Database Division for Life Science (DBCLS), BioData Science Initiative (BSI), National Institute of Genetics (NIG)". Where the former name still appears in the guidelines, please read it as the new name.

Research ID

hum0210-v2Release info

Latest

Research title

Comprehensive genomic analysis of hematological malignancies

Research overview

Aims
To perform comprehensive genomic analysis of hematological malignancies, including drug response analysis using disease models, to elucidate molecular pathogenesis and contribute to improved treatment outcomes.
Methods
Whole exome sequencing was performed for both acute myeloid leukemia cells and mediastinal germ cell tumor cells, and somatic mutations of both tumor cells were identified, using normal buccal cells as a control. RNA-seq was performed for tumour cells harvested from 5 adult T-cell leukemia/lymphoma PDX models (vehicle and MALT1 inhibitor CRD-1441551-treated, n=3 per condition).
Participants/materials
Patient with concomitant acute myeloid leukemia and mediastinal germ cell tumor, 5 PDX models of adult T-cell leukemia/lymphoma, each established from a separate patient (one model per patient).
URL
N/A

Datasets

CartDataset IDType of dataAnalysis methodAccess criteriaDate published
JGAD000297NGS (Exome)
  • WES
Controlled-access (Type I)2020-09-28
JGAD001065NGS (RNA-seq)
  • RNA-seq
Controlled-access (Type I)2026-08-03

Data provider

Principal investigator
Kazuya Shimoda
Affiliation
Division of Gastroenterology and Hematology, Department of Internal Medicine, Faculty of Medicine, University of Miyazaki

Research projects

NameURL
N/A
N/A

Grants

NameTitleProject number
National Cancer Center Research and Development Funds
Development of a comprehensive genomic profiling assay for hematological malignancies.
  • 30-A-1
Grant-in-Aid for Clinical Research from University of Miyazaki Hospital
Establishment of a method to identify high-risk groups for the development of hematological tumors.
  • 30-GH-3
Medical Research and Development Programs Focused on Technology Transfers: Development of Advanced Measurement and Analysis Systems (AMED-SENTAN), Japan Agency for Medical Research and Development (AMED)
Novel Taylor-made therapy for adult T-cell leukemia/lymphoma
  • JP18im0210102
Practical Research for Innovative Cancer Control, Japan Agency for Medical Research and Development (AMED)
Establishment of precision medicine for ATL and identification of high risk HTLV-1 carriers
  • JP19ck0106254
Practical Research for Innovative Cancer Control, Japan Agency for Medical Research and Development (AMED)
Development of MALT1 inhibitor for intractable lymphomas
  • JP20ck0106409
Practical Research for Innovative Cancer Control, Japan Agency for Medical Research and Development (AMED)
Establishment of personalized medicine for ATL based on the understanding of the genomic landscape and clonal structure
  • JP22ck0106538
Practical Research for Innovative Cancer Control, Japan Agency for Medical Research and Development (AMED)
Identification of novel therapeutic targets and development of personalized medicine for ATL
  • JP23ck0106789
KAKENHI Grant-in-Aid for Scientific Research (C)
Development of an ATL mouse model and the establishment of precision medicine that accounts for the diversity of tumor survival signals
  • 23K07840
KAKENHI Grant-in-Aid for Scientific Research (B)
Elucidation of the mechanism of ATL development through interactions with microenvironmental cells, and development of therapeutic strategies based on molecular vulnerabilities
  • 26K02444

Related publications

TitleDOIDataset ID
TP53 and PTEN mutations were shared in concurrent germ cell tumor and acute megakaryoblastic leukemia.
The requirement of MALT1 activity for the growth of adult T-cell leukemia/lymphoma

Controlled access users

No use of the controlled access data has been recorded.