4.6 Review

Modeling Pancreatic Cancer with Organoids

期刊

TRENDS IN CANCER
卷 2, 期 4, 页码 176-190

出版社

CELL PRESS
DOI: 10.1016/j.trecan.2016.03.004

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资金

  1. National Cancer Institute of the National Institutes of Health (NIH) [F32CA192904]
  2. Cold Spring Harbor Laboratory Association
  3. Carcinoid Foundation
  4. Pancreatic Cancer UK
  5. David Rubinstein Center for Pancreatic Cancer Research at Memorial Sloan Kettering Cancer Center
  6. Stand Up to Cancer/KWF
  7. STARR foundation [I7-A718]
  8. Department of Defense [W81XWH-13-PRCRP-IA]
  9. Precision Medicine Research Associates
  10. NIH [5P30CA45508-26, 5P50CA101955-07, 1U10CA180944-01, 5U01CA168409-3, 1R01CA190092-01]

向作者/读者索取更多资源

Pancreatic ductal adenocarcinoma (PDA) is a highly lethal malignancy for which new treatment and diagnostic approaches are urgently needed. For such breakthroughs to be discovered, researchers require systems that accurately model the development and biology of PDA. While cell lines, genetically engineered murine models, and xenografts have all led to valuable clinical insights, organotypic culture models have emerged as tractable systems to recapitulate the complex 3D organization of PDA. Recently, multiple methods for modeling PDA using organoids have been reported. This review aims to summarize these organoid methods in the context of other PDA models. While each model system has unique benefits and drawbacks, ultimately, organoids hold special promise for the development of personalized medicine approaches.

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