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Oncogenic Kras Activates a Hematopoietic-to-Epithelial IL-17 Signaling Axis in Preinvasive Pancreatic Neoplasia
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Many human cancers are dramatically accelerated by chronic inflammation. However, the specific cellular and molecular elements mediating this effect remain largely unknown. Using a murine model of pancreatic intraepithelial neoplasia (PanIN), we found that Kras(G12D) induces expression of functional IL-17 receptors on PanIN epithelial cells and also stimulates infiltration of the pancreatic stroma by IL-17-producing immune cells. Both effects are augmented by associated chronic pancreatitis, resulting in functional in vivo changes in PanIN epithelial gene expression. Forced IL-17 overexpression dramatically accelerates PanIN initiation and progression, while inhibition of IL-17 signaling using genetic or pharmacologic techniques effectively prevents PanIN formation. Together, these studies suggest that a hematopoietic-to-epithelial IL-17 signaling axis is a potent and requisite driver of PanIN formation.
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“Other T cell populations within the TME have all been noted to play protumorigenic roles, including Th17, Th22, CD4, and γδ T cells188–191”
From Pancreatic cancer: Advances and challenges (2023) · cites this paper as [188]
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Metadata
- Authors
- McAllister, F., Bailey, J. M., Alsina, J., Nirschl, C. J., Sharma, R., Fan, H., Rattigan, Y., Roeser, J. C., Lankapalli, R. H., Zhang, H., Jaffee, E. M., Drake, C. G., Housseau, F., Maitra, A., Kolls, J. K., Sears, C. L., Pardoll, D. M., & Leach, S. D.
- Affiliations
- Johns Hopkins University (US)
- Children's Hospital of Pittsburgh (US)
- Corresponding author
- Leach, Steven D.
- ORCID
- Venue
- Cancer Cell
- Publisher
- Elsevier BV
- Published
- 2014-05
- Volume
- 25
- Issue
- 5
- Pages
- 621-637
- ISSN
- 1535-6108 (ISSN-L)
- PMC
- PMC4072043
- OpenAlex
- W2085605492
- Cited by
- 405
- References
- 63
- Citations by year
- 2026: 21 · 2025: 27 · 2024: 39 · 2023: 37 · 2022: 43 · 2021: 38 · 2020: 44 · 2019: 37 · 2018: 15 · 2017: 32 · 2016: 29 · 2015: 29 · 2014: 14
- FWCI
- 16.71
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cancer Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Amgen
- National Cancer Institute (P01CA134292, T32CA126607, F32CA157044)
- National Institute of General Medical Sciences (T32GM066691)
- National Institute of Allergy and Infectious Diseases (T32AI007247)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK097087)
- National Center for Research Resources (S10RR017933)
- Topics
- Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
- Health Sciences › Medicine › Surgery › Pancreatitis Pathology and Treatment
- Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
- Keywords
- KRAS G12D, IL-17 signaling, pancreatic intraepithelial neoplasia, chronic pancreatitis, IL-17 receptor, pancreatic stroma, chronic inflammation, IL-17 inhibition
- MeSH terms
- Animals, Carcinoma in Situ, Cell Transformation, Neoplastic, Epithelial Cells, Hematopoietic System, Humans, Inflammation, Mice, Transgenic, Pancreas, Pancreatic Neoplasms, Signal Transduction, Proto-Oncogene Proteins p21(ras), Receptors, Antigen, T-Cell, gamma-delta, Chemoprevention, Interleukin-17, Mice, Receptors, Interleukin-17, Th17 Cells
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