TY - JOUR
T1 - The role of autophagy in pancreatic cancer
T2 - From bench to the dark bedside
AU - Görgülü, Kıvanç
AU - Diakopoulos, Kalliope N.
AU - Kaya-Aksoy, Ezgi
AU - Ciecielski, Katrin J.
AU - Ai, Jiaoyu
AU - Lesina, Marina
AU - Algül, Hana
N1 - Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/4
Y1 - 2020/4
N2 - Pancreatic cancer is one of the deadliest cancer types urgently requiring effective therapeutic strategies. Autophagy occurs in several compartments of pancreatic cancer tissue including cancer cells, cancer associated fibroblasts, and immune cells where it can be subjected to a multitude of stimulatory and inhibitory signals fine-tuning its activity. Therefore, the effects of autophagy on pancreatic carcinogenesis and progression differ in a stage and context dependent manner. In the initiation stage autophagy hinders development of preneoplastic lesions; in the progression stage however, autophagy promotes tumor growth. This double-edged action of autophagy makes it a hard therapeutic target. Indeed, autophagy inhibitors have not yet shown survival improvements in clinical trials, indicating a need for better evaluation of existing results and smarter targeting techniques. Clearly, the role of autophagy in pancreatic cancer is complex and many aspects have to be considered when moving from the bench to the bedside.
AB - Pancreatic cancer is one of the deadliest cancer types urgently requiring effective therapeutic strategies. Autophagy occurs in several compartments of pancreatic cancer tissue including cancer cells, cancer associated fibroblasts, and immune cells where it can be subjected to a multitude of stimulatory and inhibitory signals fine-tuning its activity. Therefore, the effects of autophagy on pancreatic carcinogenesis and progression differ in a stage and context dependent manner. In the initiation stage autophagy hinders development of preneoplastic lesions; in the progression stage however, autophagy promotes tumor growth. This double-edged action of autophagy makes it a hard therapeutic target. Indeed, autophagy inhibitors have not yet shown survival improvements in clinical trials, indicating a need for better evaluation of existing results and smarter targeting techniques. Clearly, the role of autophagy in pancreatic cancer is complex and many aspects have to be considered when moving from the bench to the bedside.
KW - Autophagy
KW - Pancreatic cancer
KW - Therapy
KW - Tumor microenvironment
UR - http://www.scopus.com/inward/record.url?scp=85084106928&partnerID=8YFLogxK
U2 - 10.3390/cells9041063
DO - 10.3390/cells9041063
M3 - Review article
C2 - 32344698
AN - SCOPUS:85084106928
SN - 2073-4409
VL - 9
JO - Cells
JF - Cells
IS - 4
M1 - 1063
ER -