Abstract
Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive disease, with a 5-year survival rate < 10%. Current therapies are poorly effective, thus urging the identification of new therapeutic approaches to face this lethal cancer. The RNA helicase DDX21 was recently shown to be upregulated and to associate with poor prognosis in PDAC. Our study shows that DDX21 is further upregulated in liver metastasis with respect to the primary PDAC lesions, and that depletion of DDX21 triggers autophagy while perturbing the cell cycle progression of PDAC. Together, our data support the oncogenic function of DDX21 in PDAC cells and uncover biological processes and pathways modulated by this RNA helicase.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | N/A-N/A |
| Rivista | Cancers |
| Volume | 17 |
| Numero di pubblicazione | 4 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2025 |
OSS delle Nazioni Unite
Questo processo contribuisce al raggiungimento dei seguenti obiettivi di sviluppo sostenibile
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SDG 3 Salute e benessere
All Science Journal Classification (ASJC) codes
- Oncologia
- Ricerca sul Cancro
Keywords
- autophagy
- cell cycle
- pancreatic ductal adenocarcinoma
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