
Pancreatic cancer is the most deadly of all gastrointestinal malignancies with near zero five-year survival. This review summarizes our understanding of the potentially important role of inflammation in cancer in general and pancreatic cancer in particular. Nuclear factor kappaB (NF-kappaB), a mediator of inflammatory responses, plays a significant role in carcinogenesis and is now emerging as a link between inflammation and cancer. NF-kappaB is activated in over two thirds of human pancreatic cancers; participates in early events of pancreatic carcinogenesis through its interactions with signaling pathways; and suppression of its activation restores pancreatic cell kinetics, mainly normalizing the suppressed apoptosis of pancreatic cancer. NF-kappaB is an excellent target for chemoprevention and its modulation for pancreatic cancer prevention appears promising. The next few years will likely expand our understanding of NF-kappaB biology; solidify NF-kappaB's role as a major link between chronic inflammation and pancreatic carcinogenesis; and witness the development of NF-kappaB-based approaches to pancreatic cancer prevention.
Inflammation, Nitrates, Aspirin, Anti-Inflammatory Agents, Non-Steroidal, NF-kappa B, Antineoplastic Agents, Apoptosis, Chemoprevention, Pancreatic Neoplasms, Cell Transformation, Neoplastic, Animals, Humans, Cell Proliferation
Inflammation, Nitrates, Aspirin, Anti-Inflammatory Agents, Non-Steroidal, NF-kappa B, Antineoplastic Agents, Apoptosis, Chemoprevention, Pancreatic Neoplasms, Cell Transformation, Neoplastic, Animals, Humans, Cell Proliferation
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