Nanomedicine for Imaging and Therapy of Pancreatic Adenocarcinoma.

Front Bioeng Biotechnol

Politecnico di Torino, DIMEAS, Turin, Italy.

Published: November 2019

AI Article Synopsis

  • Pancreatic adenocarcinoma has the lowest survival rate among cancers, with only about 10% of patients surviving 5 years due to its silent nature and rapid progression.
  • The tumor's dense stroma and disorganized blood vessels create significant challenges for standard chemotherapy, making treatment particularly difficult.
  • Nanomedicine offers promising solutions through nano-formulated drugs that can better penetrate barriers and monitor disease progression, leading to advancements in both treatment and early detection of metastasis.

Article Abstract

Pancreatic adenocarcinoma has the worst outcome among all cancer types, with a 5-year survival rate as low as 10%. The lethal nature of this cancer is a result of its silent onset, resistance to therapies, and rapid spreading. As a result, most patients remain asymptomatic and present at diagnosis with an already infiltrating and incurable disease. The tumor microenvironment, composed of a dense stroma and of disorganized blood vessels, coupled with the dysfunctional signal pathways in tumor cells, creates a set of physical and biological barriers that make this tumor extremely hard-to-treat with traditional chemotherapy. Nanomedicine has great potential in pancreatic adenocarcinoma, because of the ability of nano-formulated drugs to overcome biological barriers and to enhance drug accumulation at the target site. Moreover, monitoring of disease progression can be achieved by combining drug delivery with imaging probes, resulting in early detection of metastatic patterns. This review describes the latest development of theranostic formulations designed to concomitantly treat and image pancreatic cancer, with a specific focus on their interaction with physical and biological barriers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880757PMC
http://dx.doi.org/10.3389/fbioe.2019.00307DOI Listing

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