Cytokine effects on cell survival and death of A549 lung carcinoma cells
| Autor: | Georgios Chondrogiannis, Georgios Vartholomatos, Evangelos Briasoulis, Panagiotis Kanavaros, Michalis Kastamoulas, Vasiliki Galani, Dimitrios L. Arvanitis, Maria Bai |
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| Rok vydání: | 2013 |
| Předmět: |
Programmed cell death
Lung Neoplasms Time Factors Cell Survival p38 mitogen-activated protein kinases medicine.medical_treatment Blotting Western Immunology Inhibitor of apoptosis Biochemistry Cell Line Tumor medicine Humans Immunology and Allergy Molecular Biology Protein kinase B A549 cell Cell Death Chemistry Hematology Flow Cytometry Cytokine Apoptosis Cancer research Cytokines Signal transduction Signal Transduction |
| Zdroj: | Cytokine. 61:816-825 |
| ISSN: | 1043-4666 |
| DOI: | 10.1016/j.cyto.2013.01.017 |
| Popis: | Purpose IL-13, TNF-α and IL-1β have various effects on lung cancer growth and death, but the signaling pathways mediating these effects have not been extensively analyzed. Therefore, the effects of IL-13, TNF-α and IL-1β alone, and in combination with Fas, on cell viability and death as well as major signaling pathways involved in these effects were investigated in A549 lung carcinoma cells. Results Using MTT and flow cytometry, IL-13, TNF-α and IL-1β pretreatment decreased Fas-induced cell death. These anti-cell death effects were attenuated by pretreatment with inhibitors of Nuclear factor-κB [NF-κB], Phoshatidylinositole-3 kinase [PI3-K], JNK, p38 and ERK1/2 pathways. Using Western blot, IL-13, TNF-α and IL-1β treated cells showed time-dependent expression of p-ERK1/2, p-p38, p-JNK, p-Akt and p-IκBα proteins, decreased IκBα protein expression, no cleavage of Caspase-3 and PARP1 proteins and no notable alterations of Fas protein. IL-13 and TNF-α treated cells showed time-dependent increase of FLIP L expression. Conclusion IL-13, TNF-α and IL-1β attenuate the pro-cell death effects of Fas on A549 cells, at least partially, by pathways involving the NF-κB, PI3-K and MAP kinases, but not by alterations of Fas protein expression. The IL-13 and TNF-α cell survival effects may also be due to increased expression of FLIP L protein. |
| Databáze: | OpenAIRE |
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