Ontology highlight
ABSTRACT:
INSTRUMENT(S):
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Cell Culture
SUBMITTER:
Ingrid Maria Erika Ekman Stensland
LAB HEAD: Tuula A. Nyman
PROVIDER: PXD063320 | Pride | 2025-11-03
REPOSITORIES: Pride
| Action | DRS | |||
|---|---|---|---|---|
| LC-MS-files_C3.zip | Other | |||
| LC-MS-files_C4.zip | Other | |||
| LC-MS_files_C1.zip | Other | |||
| LC-MS_files_C2.zip | Other | |||
| reportC1.zip | Other |
Items per page: 5 1 - 5 of 8 |

Amrutkar Manoj M Li Yuchuan Y Finstadsveen Anette Vefferstad AV Verbeke Caroline S CS Gladhaug Ivar P IP
Proteomes 20251001 4
<h4>Background</h4>Gemcitabine (GEM) remains a cornerstone in the treatment of pancreatic cancer. Upon exposure to GEM, pancreatic cancer cells (PCCs) tend to adapt quickly to outcompete drug-induced cytotoxicity, thereby contributing to treatment failure. Thus, understanding GEM-induced molecular changes in PCCs is important.<h4>Methods</h4>Three primary PCC lines (PCC-1, PCC-2, PCC-7) and Mia PaCa-2 cultured for 40 passages (p) in the absence (control) or presence of GEM (GemR) were assessed f ...[more]