NBDC Research ID: hum0427.v2

 

SUMMARY

Aims:

- Head and neck malignancies originate in a wide variety of locations, including the pharynx, larynx, oral cavity, nose and paranasal sinuses, salivary glands, thyroid gland, and temporal bone. Their molecular biological characteristics differ depending on the location of origin. Therefore, it is necessary to establish a tailored treatment that is tailored to the molecular biological characteristics of each tumor. In the field of oncology, many researchers generally use cell lines obtained from cell banks. However, cell lines for head and neck malignancies available from cell banks are limited especially for rare-type cancers, resulting in difficulties in elucidation of biological characterization of such malignancies and establishment of therapeutic strategies. This study aimed to 1) conduct comprehensive genetic analysis of head and neck malignant tumor tissues and patient-derived blood, 2) establish cell lines of head and neck malignancies and to examine their tumorigenic abilities in immune-deficient animals, 3) deposit to cell banks. Using multi-omics approaches, we seek to elucidate the molecular mechanisms of oncogenes and to develop biomarkers for recurrence and metastasis prediction, as well as strategies for novel targeted therapies.

Methods:

- Genomic DNAs extracted from peripheral blood mononuclear cells (PBMC), the primary tumor tissues, and the cell line were used for whole exome sequencing analysis.

- Chromatin immunoprecipitation (ChIP) sequencing using H3K27Ac and YAP antibodies

Participants/Materials:

- PBMC and the primary tumor tissues were collected from a patient with external auditory canal squamous cell carcinoma, and a cell line was established from the primary tumor tissues. The cell line was deposited as SCEACono2 in RIKEN BioResource Research Center (https://cellbank.brc.riken.jp/cell_bank/CellInfo/?cellNo=RCB5515&lang=En).

- Five patients with temporal bone squamous cell carcinoma

 

Dataset IDType of DataCriteriaRelease Date
JGAS000645 NGS (Exome) Controlled-access (Type I) 2023/11/02
JGAS000645 (Data addition) NGS (ChIP-seq) Controlled-access (Type I) 2026/06/16

*Release Note

*Data users need to apply an application for Using NBDC Human Data to reach the Controlled-access Data. Learn more

 

MOLECULAR DATA

JGAS000645 (Exome)

Participants/Materials

external auditory canal squamous cell carcinoma (ICD10: C44.2): 1 case (3 samples)

    non-tumor tissue (PBMC), primary tumor tissue, cell line established from the primary tumor tissue: 1 sample each

Targets Exome
Target Loci for Capture Methods -
Platform MGI [DNBSEQ-G400]
Library Source DNAs extracted from PBMC, the primary tumor tissues, and the cell line
Cell Lines -
Library Construction (kit name) SureSelect Human All Exon V6 Kit
Fragmentation Methods Ultrasonic fragmentation (Covaris)
Spot Type Paired-end
Read Length (without Barcodes, Adaptors, Primers, and Linkers) 100 bp
Japanese Genotype-phenotype Archive Dataset ID JGAD000775
Total Data Volume 29.6 GB (fastq)
Comments (Policies) NBDC policy

 

JGAS000645 (ChIP-seq)

Participants/Materials

Temporal bone squamous cell carcinoma (ICD10: C44.2): 5 cases

[H3K27Ac]

    primary tumor tissues: 5 samples

    non-tumor tissues (normal skin): 2 samples

[YAP]

    primary tumor tissues: 2 samples

    non-tumor tissues (normal skin): 2 samples

Pooled input DNA obtained by mixing DNA from all patients: 1 sample

Targets ChIP-seq
Target Loci for Capture Methods -
Platform Illumina [NextSeq 500]
Library Source DNAs extracted from tumor and non-tumor tissues of patients with temporal bone squamous cell carcinoma, and immunoprecipitated with an anti-H3K27Ac and YAP antibody
Cell Lines -
Library Construction (kit name) DNA Library Prep Kit for Illumina
Fragmentation Methods Ultrasonic fragmentation
Spot Type Single-end
Read Length (without Barcodes, Adaptors, Primers, and Linkers) 75 bp
Japanese Genotype-phenotype Archive Dataset ID JGAD000775
Total Data Volume 25.0 GB (fastq)
Comments (Policies) NBDC policy

 

DATA PROVIDER

Principal Investigator: Takashi Nakagawa

Affiliation: Department of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University

Project / Group Name: -

Funds / Grants (Research Project Number):

NameTitleProject Number
KAKENHI Grant-in-Aid for Scientific Research (B) Development of novel synthesizing treatment strategy by exhaustive research on temporal bone squamous cell carcinoma 18H02951
KAKENHI Grant-in-Aid for Scientific Research (B) Elucidation of epigenetic tumor control mechanisms that determine the malignancy of squamous cell carcinoma of the temporal bone 22H03236
KAKENHI Grant-in-Aid for Scientific Research (C) Elucidation of the Metastasis Regulatory Mechanism via NLRP3 Inflammasome Pathway in Temporal Bone Squamous Cell Carcinoma 22K09745
KAKENHI Grant-in-Aid for Early-Career Scientists Investigation of transcriptional reprogramming mechanisms involved in invasion and metastasis of head and neck squamous cell caricnoma 20K18300
Research Grant, Soda Toyoji Memorial Foundation Elucidation of Transcriptional Regulatory Mechanisms Contributing to the Progression of Squamous Cell Carcinoma of the External Auditory Canal via Multi-omics Analysis -
Medical Research Grant, Takeda Science Foundation Elucidation of the YAP1-mediated transcriptional reprogramming mechanism contributing to invasion and metastasis in head and neck squamous cell carcinoma -
Cancer Research Grant, Shinnihon Foundation of Advanced Medical Treatment Research Exploring Transcriptional Reprogramming Mechanisms Underlying Head and Neck Cancer Progression via Multi-omics Analysis -
Cancer Research Grant, SGH Foundation Elucidation of Transcriptional Reprogramming Mechanisms involved in Invasion and Metastasis in Head and Neck Squamous Cell Carcinoma -

 

PUBLICATIONS

TitleDOIDataset ID
1 Establishment and characterization of a primary cell culture derived from external auditory canal squamous cell carcinoma doi: 10.1002/2211-5463.13225 JGAD000775
2 Aberrant Hippo-YAP/TEAD Signaling Drives Malignant Transcriptional Reprogramming in External Auditory Canal Squamous Cell Carcinoma doi: 10.1158/2767-9764.CRC-25-0626 JGAD000775

 

USRES (Controlled-access Data)

Principal InvestigatorAffiliationCountry/RegionResearch TitleData in Use (Dataset ID)Period of Data Use