Research ID
hum0143-v1Release info
Research title
Aberrant (pro)renin receptor expression induces genomic instability by chromatin remodeler SMARCA5 disruption during the pancreatic ductal adenocarcinoma
Research overview
- Aims
- The aim of the present study is to elucidate whether aberrant (P)RR expression induces genomic instability in human pancreatic ductal epithelial (HPDE) cells, which are transforming into pancreatic ductal adenocarcinoma (PDAC).
- Methods
- Comparative analysis of the human whole genome between HPDE cells overexpressed by(pro)renin receptor and control HPDE cells
- Participants/materials
- Immortalized human pancreatic ductal epithelial (HPDE) cells
- URL
- N/A
Datasets
| Cart | Dataset ID | Type of data | Analysis method | Access criteria | Date published |
|---|---|---|---|---|---|
| JGAD000212 | NGS (WGS) |
| Controlled-access (Type I) | 2025-05-13 |
Data provider
- Principal investigator
- Akira Nishiyama
- Affiliation
- Department of Pharmacology, Faculty of Medicine, Kagawa Universty
Research projects
No research projects.
Grants
| Name | Title | Project number |
|---|---|---|
KAKENHI Grant-in-Aid for Scientific Research (B) | Kidney-mediated aging process |
|
KAKENHI Grant-in-Aid for Scientific Research (C) | Evolutionary machanism of pancreatic ductal adenocarcinoma mediated by (pro)renin receptor |
|
KAKENHI Grant-in-Aid for challenging Exploratory Research | Functional analysis of (pro)renin receptor in the genesis of pancreatic cancer |
|
Hoansha Foundation and Alumni Association of Kagawa University (Sanjukai) | Development of new therapeutic agents for lifestyle-related diseases | N/A |
TOBIRA, Tokyo Biomarker Innovation Research Associate | Examination of the availability of soluble (pro)renin receptor as an early marker of pancreatic cancer | N/A |
Related publications
| Title | DOI | Dataset ID |
|---|---|---|
Aberrant (pro)renin receptor expression induces genomic instability in pancreatic ductal adenocarcinoma through upregulation of SMARCA5/SNF2H |
Controlled access users
No use of the controlled access data has been recorded.