Pomalidomide Alters Pancreatic Macrophage Populations to Generate an Immune-Responsive Environment at Precancerous and Cancerous Lesions

During development of pancreatic cancer, alternatively activated macrophages contribute to fibrogenesis, pancreatic intraepithelial neoplasia (PanIN) lesion growth, and generation of an immunosuppressive environment. Here, we show that the immunomodulatory agent pomalidomide depletes pancreatic lesi...

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Bibliographic Details
Published in:Cancer research (Chicago, Ill.) Ill.), 2019-04, Vol.79 (7), p.1535-1548
Main Authors: Bastea, Ligia I, Liou, Geou-Yarh, Pandey, Veethika, Fleming, Alicia K, von Roemeling, Christina A, Doeppler, Heike, Li, Zhimin, Qiu, Yushi, Edenfield, Brandy, Copland, John A, Tun, Han W, Storz, Peter
Format: Article
Language:English
Subjects:
Animals
Humans
Immunologic Factors - pharmacology
Interferon Regulatory Factors - metabolism
Macrophages - immunology
Mice
Pancreatic Neoplasms - immunology
Pancreatic Neoplasms - metabolism
Precancerous Conditions - immunology
Precancerous Conditions - metabolism
Thalidomide - analogs & derivatives
Thalidomide - pharmacology
Tumor Microenvironment
U937 Cells
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Summary:During development of pancreatic cancer, alternatively activated macrophages contribute to fibrogenesis, pancreatic intraepithelial neoplasia (PanIN) lesion growth, and generation of an immunosuppressive environment. Here, we show that the immunomodulatory agent pomalidomide depletes pancreatic lesion areas of alternatively activated macrophage populations. Pomalidomide treatment resulted in downregulation of interferon regulatory factor 4, a transcription factor for M2 macrophage polarization. Pomalidomide-induced absence of alternatively activated macrophages led to a decrease in fibrosis at PanIN lesions and in syngeneic tumors; this was due to generation of an inflammatory, immune-responsive environment with increased expression of IL1α and presence of activated (IFNγ-positive) CD4 and CD8 T-cell populations. Our results indicate that pomalidomide could be used to decrease fibrogenesis in pancreatic cancer and may be ideal as a combination treatment with chemotherapeutic drugs or other immunotherapies. SIGNIFICANCE: These findings reveal new insights into how macrophage populations within the pancreatic cancer microenvironment can be modulated, providing the means to turn the microenvironment from immunosuppressive to immune-responsive.
ISSN:0008-5472
1538-7445
DOI:10.1158/0008-5472.CAN-18-1153