Cell line · CVCL_0152
AsPC-1
Cancer cell line, Homo sapiens. Pancreatic ductal adenocarcinoma. 220 papers.
4 sourcescell-lines-2026-11-14-0.1.0
Cite this record
ConductScience Library. AsPC-1. Cell lines, record CVCL_0152. Release cell-lines-2026-11-14-0.1.0, 14 Nov 2026. https://conductscience.org/library/cell-lines/CVCL_0152
On this page
Cell line
As Cellosaurus gives it.
- Name
- AsPC-1
- Accession
- CVCL_0152
- RRID
- RRID:CVCL_0152
- Synonyms
- AsPc-1, Aspc-1, ASPC-1, As-PC1, ASPC1, AsPC1, Aspc1, AsPc1
- Species
- Homo sapiens (Human)
- Sex
- Female
- Age at sampling
- 62Y
- Category
- Cancer cell line
- Diseases
- Pancreatic ductal adenocarcinoma (NCIt C9120)
- Derived from
- Ascites (metastatic)
- Entry created
- 2012-04-04
- Entry updated
- 2026-06-25
Source Cellosaurus
Problems1
| Problem | Cellosaurus's note |
|---|---|
| Caution | TP53 mutation indicated incorrectly as being at c.818G>A in PubMed=1630814. |
Source Cellosaurus
Papers220
| Paper | Journal | Year | How we know | Retracted | Source |
|---|---|---|---|---|---|
| Long Noncoding RNA LINC00941 Links Oncogenic KRAS Signaling to Aggressiveness, DNA Repair, and Chemoresistance in Pancreatic Cancer | IUBMB Life | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Pharmacokinetic Tuning Redirects β‐Lapachone From NQO1 Bioactivation to Vimentin‐Targeted Oxidation in Cancer | Adv Sci (Weinh) | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Selective AUTAC-mediated ATP7B degradation unlocks cuproptosis vulnerability in pancreatic ductal adenocarcinoma. | Clin Transl Med | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Targeting SERPINB5 and MSLN for Pancreatic Cancer Therapy. | Cancers (Basel) | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Differential Sensitivity to xCT-inhibition by ME1 expression. | Mol Cancer Ther | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Dual Targeting of FGFR4 and PI3K-mTOR Suppresses Tumor-Associated Phenotypes in Pancreatic Ductal Adenocarcinoma. | Int J Mol Sci | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Discovery and Optimization of AMT-676, a CDH17-Targeting ADC for the Treatment of Advanced Gastrointestinal Cancers. | Adv Sci (Weinh) | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Activation of PP2A-B56a leads to aberrant EGFR signaling and proliferative phenotypes in PDAC. | Mol Cancer Ther | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Targeting Oncogenic KRAS Using Peptide Nucleic Acid Oligomers Attached to Cell-Penetrating Peptides. | Int J Mol Sci | 2026 | Its Methods give the RRID and name the line | PubMed | |
| Glutamine-restricted diets restore sensitivity to KRASG12D inhibitor through the reversal of ANXA1 mediated metabolic reprogramming. | Cell Rep Med | 2026 | Its Methods give the RRID and name the line | PubMed |
1 to 10 of 220
See all 220 papersRelatives13
| Relation | Cell line | Accession | Problem | Source |
|---|---|---|---|---|
| Derived from it | AsPC-1 SPINK1 #10 | CVCL_C3NE | Cell lines | |
| Derived from it | AsPC-1/CMV-Luc | CVCL_J243 | Cell lines | |
| Derived from it | AsPC1-R | CVCL_XX79 | Cell lines | |
| Derived from it | AsPC1/GFP | CVCL_E6XM | Cell lines | |
| Derived from it | AsPC1/Luciferase-2A-GFP | CVCL_E6XP | Cell lines | |
| Derived from it | AsPC1/RFP | CVCL_E6XN | Cell lines | |
| Derived from it | EDITGENE AsPC-1-CopGFP | CVCL_F6BH | Cell lines | |
| Derived from it | EDITGENE AsPC-1-FLUC | CVCL_F5TV | Cell lines | |
| Derived from it | EDITGENE GPER1 Knockout AsPC-1 Cell Line | CVCL_F5BZ | Cell lines | |
| Derived from it | HyCyte AsPC-1 KO-hCDH17 | CVCL_F1MR | Cell lines |
1 to 10 of 13
See all 13 relativesCell banks10
| Cell bank | Catalog number | Status | Source |
|---|---|---|---|
| ATCC | CRL-1682 | ATCC | |
| AddexBio | C0018023/5061 | Cellosaurus | |
| BCRC | 60494 | BCRC | |
| CLS | 300158 | CLS | |
| ECACC | 96020930 | ECACC | |
| EDITGENE | EDC00327 | EDITGENE | |
| IBRC | C10154 | Cellosaurus | |
| IZSLER | BS TCL 171 | Cellosaurus | |
| KCLB | 21682 | KCLB | |
| NCBI_Iran | C558 | Cellosaurus |
Data dates
The date of each source this release read.
Sources 4
- CellosaurusCC BY 4.0, with credit to Cellosaurus (SIB)
- PubMed Central's articlesTitles shown only for CC0, CC BY and public domain articles
- NLM's PMC Article DatasetsCourtesy of NLM, which does not endorse this database
- PubMedNLM's terms
Each source's terms
- CellosaurusCC BY 4.0. Cellosaurus's README: "we have chosen to apply the Creative Commons Attribution 4.0 International (CC BY 4.0) license to Cellosaurus (https://creativecommons.org/licenses/by/4.0/). This means that you are free to copy and redistribute Cellosaurus in any medium or format. You can remix, transform, and build upon Cellosaurus for any purpose, even commercially. You must give appropriate credit, provide a link to the license, and indicate if changes were made." Copyright (c) CALIPHO group, SIB Swiss Institute of Bioinformatics. Read on 14 Nov 2026 at https://ftp.expasy.org/databases/cellosaurus/README
- PubMed Central's articlesEach article's own license. Its words show only under CC0, CC BY or public domain
- NLM's PMC Article DatasetsNLM's PMC Article Datasets on AWS, https://registry.opendata.aws/ncbi-pmc. Its terms: users "acknowledge NLM as the source of the data in a clear and conspicuous manner", do not use the PubMed Central wordmark or the PMC logo, do not "indicate or imply that NLM/NIH/HHS has endorsed" a product, and "only distribute data that are licensed for redistribution". Each article keeps its own license: https://pmc.ncbi.nlm.nih.gov/about/copyright/
- PubMedNLM's terms
Cellosaurus, SIB Swiss Institute of Bioinformatics, https://www.cellosaurus.org, CC BY 4.0. Its problem notes are given in its own words.
For software
Read this cell line from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/cell-lines/v1/CVCL_0152
GET https://conductscience.org/api/cell-lines/v1/CVCL_0152/papers?page=2