FOXP3 EXPRESSION IN HUMAN CANCER CELLS

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FOXP3 EXPRESSION IN HUMAN CANCER CELLS Vaios Karanikas EU Marie Curie Fellow Cancer Immunology Unit Department of Immunology and Histocompatibility School of Medicine University of Thessaly Larissa, Greece

Foxp3: The gene FoxP3 LAG-3 CD25: α chain of the IL-2 receptor FoxP3: transcription factor that inhibits expression of cytokine genes LAG-3 (CD223): homologous to CD4; binds to HLA

Foxp3: The gene Transcription factor that is characteristic of natural T regulatory cells (ntregs) Activated CD4 + CD25 - and CD8 + CD25 - T cells can acquire a regulatory phenotype by expressing Foxp3, which results in reducing their functional reactivity T cells derived from Foxp3 Tg mice (over-expression of Foxp3) cannot be easily stimulated through TcR cross-linking T cells derived from Foxp3 Tg mice (mutation of Foxp3, scurfy mice) are in a state of constant activation

Foxp3: Function in Tregs Transcriptional activation of cell surface molecules such as CD25, GITR, CTLA-4 και CD103 GITR CTLA-4 Transcriptional regression of gene expression (IL-2, ΙL-4 and IFN-γ)

Foxp3: The gene/protein Expression of Foxp3 only on CD4 + T cells Low or no transcripts expressed by other lymphocytes (B, CD8 etc) Low or no transcripts expressed by other tissue cells Expression of Foxp3 in Tregs is a result of gene demethylation Foxp3 participates in immune escape

Hypothesis Foxp3 promoter demethylation in cancer cells can result in the expression of Foxp3 protein and/or other factors with a suppressive function Aim To search for Foxp3 transcripts and protein in cancer cells of various origins

Materials

Methods Foxp3 mrna Conventional PCR (b-actin) Real Time PCR (β2m) Protein Immunohistochemistry (clone 236A/E7, Bioscience) Flow cytometry (clone PCH101, Bioscience)

Results: Foxp3 transcripts No increased expression of TGF-b or IL10 Treatment with 5-aza CdR or TSA causes no alteration in expression of Foxp3, TGF-b or IL10

Results: Foxp3 protein Melanoma T leukemia Lung Cancer Breast Cancer Colon Cancer EBV transformed B cells

Results: Foxp3 protein

Concluding Remarks Foxp3 is expressed at the transcript and protein level in cancer cells Although Foxp3 expression is lesser than Tregs, its protein levels are significantly high enough Expression of Foxp3 does not seem to alter after treatment with epigenetic drugs Expression of Foxp3 levels does not seem to correlate with TGF-b and IL10 expression levels What is the role of Foxp3 in cancer cells?

Thank you for your attention Cancer Immunology Unit, Department of Immunology and Histocompatibility, School of Medicine, University of Thessaly, Larissa, Greece: Vaios Karanikas, Speletas Matthaios, Zamanakou Maria, Kalala Fani, Loules Gideon, Germenis Anastasios Department of Respiratory Medicine, School of Medicine, University of Thessaly: Kerenidi Theodora, Gourgoulianis Konstantinos Genetic and Cellular Unit, Ludwig Institute for Cancer Research, Belgium: Pierre Coulie Cancer Trials Laboratory, Austin Research Institute, Melbourne, Australia: Bruce Loveland Funding: This work was supported by a) a Marie Curie Incoming International al Fellowship within the 6th European Community Framework Programme (MIF1-CT CT-2006-021795) 021795) GRANT, b) a E.U-European European Social Fund (70%), the Greek Ministry of Development-GSRT (30%) & Antisel (10%)(EPAN05 NON-EU EU-445) grant and c) a Glaxo Smith Kline Hellas Research Fellowship (Program No3116) grant

Results: Foxp3 in tissues