Ontology highlight
ABSTRACT:
INSTRUMENT(S):
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Pancreatic Ductal Cell, Cell Culture
DISEASE(S): Pancreatic Ductal Adenocarcinoma
SUBMITTER:
Krystine Mansfield
LAB HEAD: Patrick Pirrotte
PROVIDER: PXD060475 | Pride | 2025-10-13
REPOSITORIES: Pride
Items per page: 5 1 - 5 of 70 |

Shen Changxian C Cui Tiantian T Yang Linlin L Gui Ling L Corrales-Guerrero Sergio S Nair Sindhu S Li Haiqing H Karasinska Joanna M JM Topham James T JT Renouf Daniel J DJ Schaeffer David F DF Fernandez Anthony A Ping Xiaoli X Shen Binghui B Stark Jeremy M JM Williams Terence M TM
Nucleic acids research 20250901 18
KRAS activating mutations occur in 90%-95% of pancreatic adenocarcinoma (PC) and contribute to tumor progression and resistance to therapy, including radiotherapy. A screen in isogenic cells revealed that KRAS activation positively modulates STN1 expression, a component of the CTC1-STN1-TEN1 (CST) complex. We find that STN1 is significantly upregulated in PC and its elevation is correlated with KRAS oncogenic mutations, while inhibition of KRAS signaling decreases STN1 expression. Interestingly, ...[more]