TY - JOUR
T1 - DDX21 Controls Cell Cycle Progression and Autophagy in Pancreatic Cancer Cells
AU - Leccese, Adriana
AU - Ruta, Veronica
AU - Panzeri, Valentina
AU - Attili, Fabia
AU - Spada, Cristiano
AU - Cianfanelli, Valentina
AU - Sette, Claudio
PY - 2025
Y1 - 2025
N2 - 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.
AB - 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.
KW - autophagy
KW - cell cycle
KW - pancreatic ductal adenocarcinoma
KW - autophagy
KW - cell cycle
KW - pancreatic ductal adenocarcinoma
UR - https://publicatt.unicatt.it/handle/10807/313333
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85218910676&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85218910676&origin=inward
U2 - 10.3390/cancers17040570
DO - 10.3390/cancers17040570
M3 - Article
SN - 2072-6694
VL - 17
SP - N/A-N/A
JO - Cancers
JF - Cancers
IS - 4
ER -