AI Article Synopsis

  • Pancreatic cancer is becoming more common and is often diagnosed late, leading to a poor outlook for patients, with treatments not being very effective due to the disease's complexity.
  • Recent research has advanced our understanding of the biology and genetics of pancreatic cancer, allowing for better classification and potential treatment options.
  • The review covers the role of biological features, metabolic changes, and the tumor microenvironment in cancer development, along with emerging biomarkers, treatment responses, and challenges in developing new therapies.

Article Abstract

Pancreatic cancer is an increasingly common cause of cancer mortality with a tight correspondence between disease mortality and incidence. Furthermore, it is usually diagnosed at an advanced stage with a very dismal prognosis. Due to the high heterogeneity, metabolic reprogramming, and dense stromal environment associated with pancreatic cancer, patients benefit little from current conventional therapy. Recent insight into the biology and genetics of pancreatic cancer has supported its molecular classification, thus expanding clinical therapeutic options. In this review, we summarize how the biological features of pancreatic cancer and its metabolic reprogramming as well as the tumor microenvironment regulate its development and progression. We further discuss potential biomarkers for pancreatic cancer diagnosis, prediction, and surveillance based on novel liquid biopsies. We also outline recent advances in defining pancreatic cancer subtypes and subtype-specific therapeutic responses and current preclinical therapeutic models. Finally, we discuss prospects and challenges in the clinical development of pancreatic cancer therapeutics.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255319PMC
http://dx.doi.org/10.1038/s41392-021-00659-4DOI Listing

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