TY - JOUR
T1 - Pancreatic Ductal Adenocarcinoma and Nutrition: Exploring the Role of Diet and Gut Health
AU - Gualtieri, P.
AU - Cianci, Rossella
AU - Frank, G.
AU - Pizzocaro, E.
AU - De, Santis G. L.
AU - Giannattasio, S.
AU - Merra, G.
AU - Butturini, G.
AU - De, Lorenzo A.
AU - Di, Renzo L.
PY - 2023
Y1 - 2023
N2 - The incidence of pancreatic cancer is increasing worldwide. The most common form is represented by pancreatic ductal adenocarcinoma (PDAC) which has been shown to be linked to chronic inflammation. Notably, the gut microbiota has emerged as a critical player in regulating immune responses and inflammation. Indeed, intestinal dysbiosis, characterized by an imbalance in the gut microbiota composition, can contribute to the initiation of chronic inflammation. Sterile chronic inflammation can occur, probably activated by the translocation of bacterial components, such as lipopolysaccharide (LPS), the major component of Gram-negative microbiota, with the consequent induction of innate mucosal immunity, through the activation of Toll-like receptors (TLRs). Furthermore, the interaction between LPS and TLRs could enhance cancer progression. Recent research has shed light on the pivotal role of nutrition, as a modifiable risk factor, in PDAC immunological processes, particularly focusing on the immuno-modulatory effects of the gut microbiota. Different dietary regimens, fiber intake, immunonutrients, and antioxidants have the potential to either exacerbate or mitigate chronic inflammation, thereby influencing the pathogenesis and natural history of PDAC. These dietary components may affect the gut microbiota composition and, consequently, the level of inflammation, either promoting or protecting against PDAC. In this review of reviews, we discuss the modulatory role of nutrition and the gut microbiota in PDAC’s immunological processes to explore a translational therapeutic approach that could improve the survival and quality of life of these patients.
AB - The incidence of pancreatic cancer is increasing worldwide. The most common form is represented by pancreatic ductal adenocarcinoma (PDAC) which has been shown to be linked to chronic inflammation. Notably, the gut microbiota has emerged as a critical player in regulating immune responses and inflammation. Indeed, intestinal dysbiosis, characterized by an imbalance in the gut microbiota composition, can contribute to the initiation of chronic inflammation. Sterile chronic inflammation can occur, probably activated by the translocation of bacterial components, such as lipopolysaccharide (LPS), the major component of Gram-negative microbiota, with the consequent induction of innate mucosal immunity, through the activation of Toll-like receptors (TLRs). Furthermore, the interaction between LPS and TLRs could enhance cancer progression. Recent research has shed light on the pivotal role of nutrition, as a modifiable risk factor, in PDAC immunological processes, particularly focusing on the immuno-modulatory effects of the gut microbiota. Different dietary regimens, fiber intake, immunonutrients, and antioxidants have the potential to either exacerbate or mitigate chronic inflammation, thereby influencing the pathogenesis and natural history of PDAC. These dietary components may affect the gut microbiota composition and, consequently, the level of inflammation, either promoting or protecting against PDAC. In this review of reviews, we discuss the modulatory role of nutrition and the gut microbiota in PDAC’s immunological processes to explore a translational therapeutic approach that could improve the survival and quality of life of these patients.
KW - chronic inflammation
KW - dysbiosis
KW - gut microbiota
KW - immunonutrition
KW - pancreatic ductal adenocarcinoma
KW - chronic inflammation
KW - dysbiosis
KW - gut microbiota
KW - immunonutrition
KW - pancreatic ductal adenocarcinoma
UR - https://publicatt.unicatt.it/handle/10807/269932
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85175278878&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85175278878&origin=inward
U2 - 10.3390/nu15204465
DO - 10.3390/nu15204465
M3 - Article
SN - 2072-6643
VL - 15
SP - 1
EP - 19
JO - Nutrients
JF - Nutrients
IS - 20
ER -