4.7 Review

Pancreatic cancer: Stroma and its current and emerging targeted therapies

Journal

CANCER LETTERS
Volume 391, Issue -, Pages 38-49

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2016.12.035

Keywords

Pancreatic Cancer; Tumor microenvironment; Stroma; Targeted therapies; miRNAS

Categories

Funding

  1. Elsa U. Pardee Foundation
  2. Showalter Trust Foundation
  3. American Cancer Society Institutional Research Grant
  4. IUPUI Center for Pancreatic Cancer Research
  5. IU Simon Cancer Center
  6. Indiana Clinical and Translational Sciences Institute
  7. IU School of Medicine Biomedical Research Grant
  8. DeVault Foundation
  9. Cagiantas Scholarship
  10. Public Health Services Research grant [R01 CA-075059]

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Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal human malignancies with a 5-year survival rate of 8%. Dense, fibrotic stroma associated with pancreatic tumors is a major obstacle for drug delivery to the tumor bed and plays a crucial role in pancreatic cancer progression. Targeting stroma is considered as a potential therapeutic strategy to improve anti-cancer drug efficacy and patient survival. Although numerous stromal depletion therapies have reached the clinic, they add little to overall survival and are often associated with toxicity. Furthermore, increasing evidence suggests the anti-tumor properties of stroma. Its complete ablation enhanced tumor progression and reduced survival. Consequently, efforts are now focused on developing stromal-targeted therapies that normalize the reactive stroma and avoid the extremes: stromal abundance vs. complete depletion. In this review, we summarized the state of current and emerging anti-stromal targeted therapies, with major emphasis on the role of miRNAs in PDAC stroma and their potential use as novel therapeutic agents to modulate PDAC tumor-stromal interactions. (C) 2017 Elsevier B.V. All rights reserved.

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