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- W4366281330 endingPage "2354" @default.
- W4366281330 startingPage "2354" @default.
- W4366281330 abstract "An overabundance of desmoplasia in the tumour microenvironment (TME) is one of the defining features that influences pancreatic ductal adenocarcinoma (PDAC) development, progression, metastasis, and treatment resistance. Desmoplasia is characterised by the recruitment and activation of fibroblasts, heightened extracellular matrix deposition (ECM) and reduced blood supply, as well as increased inflammation through an influx of inflammatory cells and cytokines, creating an intrinsically immunosuppressive TME with low immunogenic potential. Herein, we review the development of PDAC, the drivers that initiate and/or sustain the progression of the disease and the complex and interwoven nature of the cellular and acellular components that come together to make PDAC one of the most aggressive and difficult to treat cancers. We review the challenges in delivering drugs into the fortress of PDAC tumours in concentrations that are therapeutic due to the presence of a highly fibrotic and immunosuppressive TME. Taken together, we present further support for continued/renewed efforts focusing on aspects of the extremely dense and complex TME of PDAC to improve the efficacy of therapy for better patient outcomes." @default.
- W4366281330 created "2023-04-20" @default.
- W4366281330 creator A5021597572 @default.
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- W4366281330 creator A5041714935 @default.
- W4366281330 creator A5051540542 @default.
- W4366281330 creator A5080435709 @default.
- W4366281330 date "2023-04-18" @default.
- W4366281330 modified "2023-09-26" @default.
- W4366281330 title "Overcoming the Fibrotic Fortress in Pancreatic Ductal Adenocarcinoma: Challenges and Opportunities" @default.
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