NBDC Research ID: hum0088.v1
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SUMMARY
Aims: To elucidate the effect and its mechanism of BMP signaling on glioma initiating cells
Methods: Target genes were identified by RNA-seq to elucidate the mechanism of regulation of glioma initiating cells by BMP. Genomic DNA was extracted from glioma initiating cells and whole genome sequencing was performed.
Participants/Materials: Patient-derived glioblastoma cell lines (tumor initiating cells), 2 lines
Dataset ID | Type of Data | Criteria | Release Date |
---|---|---|---|
JGAS000077 | NGS (RNA-seq) | Controlled-access (Type I) | 2019/02/08 |
JGAS000096 | NGS (WGS) | Controlled-access (Type I) | 2019/02/08 |
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MOLECULAR DATA
Participants/Materials | 2 glioblastomas (ICD10:C71.9) (TGS-01, TGS-04) |
Targets | RNA-seq |
Target Loci for Capture Methods | - |
Platform |
Illumina [Genome Analyzer IIx] Thermo Fisher Scientific [IonProton] |
Library Source | glioblastoma cell lines were stimulated with BMP-4 for 24 h prior to RNA extraction |
Cell Lines | - |
Library Construction (kit name) |
ScriptSeq v2 RNA-seq Library Preparation Kit (Epicentre) Ion Total RNA-seq Kit v2 (Thermo Fisher Scientific) |
Fragmentation Methods |
Genome Analyzer IIx: Enzymatic Shearing (included in the kit) IonProton: Enzymatic Shearing (included in the kit: RNase III) |
Spot Type |
Genome Analyzer IIx: Paired-end IonProton: Single-end |
Read Length (without Barcodes, Adaptors, Primers, and Linkers) |
Genome Analyzer IIx: 76 bp IonProton: 200 bp |
Japanese Genotype-phenotype Archive Dataset ID | JGAD000077 |
Total Data Volume | 43 GB (fastq) |
Comments (Policies) | NBDC policy |
Participants/Materials | 1 glioblastoma (ICD10:C71.9) (TGS-01) |
Targets | WGS |
Target Loci for Capture Methods | - |
Platform | Thermo Fisher Scientific [IonProton] |
Library Source | gDNA extracted from glioblastoma cell line (tumor initiating cells) |
Cell Lines | - |
Library Construction (kit name) |
Ion Fragment plus library Kit Ion PI Template OT2 200 Kit v3 Ion PI Sequencing 200 Kit v3 (Thermo Fisher Scientific) |
Fragmentation Methods | Ultrasonic fragmentation (Bioruptor UCD-200) |
Spot Type | Single-end |
Read Length (without Barcodes, Adaptors, Primers, and Linkers) | 200 bp |
Japanese Genotype-phenotype Archive Dataset ID | JGAD000096 |
Total Data Volume | 13 GB (fastq) |
Comments (Policies) | NBDC policy |
DATA PROVIDER
Principal Investigator: Kohei Miyazono
Affiliation: Department of Molecular Pathology, Graduate School of Medicine, The University of Tokyo
Project / Group Name: -
Funds / Grants (Research Project Number):
Name | Title | Project Number |
---|---|---|
KAKENHI Grant-in-Aid for Scientific Research on Innovative Areas | Effects of TGF-β family on cancer microenvironment and strategies for cancer therapy | 22112002 |
KAKENHI Grant-in-Aid for Scientific Research (B) | Roles of BMP signaling in maintenance of cell stemness | 24390070 |
KAKENHI Grant-in-Aid for Scientific Research (S) | Transcriptional regulation by TGF-β signaling and its relation to progression of cancer | 15H05774 |
JSPS Core-to-Core Program | Cooperative International Framework in TGF-beta Family Signaling | - |
PUBLICATIONS
Title | DOI | Dataset ID | |
---|---|---|---|
1 | Bone morphogenetic protein signaling mediated by ALK-2 and DLX2 regulates apoptosis in glioma-initiating cells. | doi: 10.1038/onc.2017.112 | JGAD000077 |
2 | Identification of a novel fusion gene HMGA2-EGFR in glioblastoma. | doi: 10.1002/ijc.31179 |
JGAD000077 JGAD000096 |
USRES (Controlled-access Data)
Principal Investigator: | Affiliation: | Data in Use (Dataset ID) | Period of Data Use |
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