Effects of ascorbic acid on tax, NF-κB and MMP-9 in human T-cell lymphotropic virus type 1 positive malignant T-lymphocytes
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Bentham Science Publishers B.V.
Abstract
Background: HTLV1 is a retrovirus that infects CD4-positive cells and leads to Adult T-cell leukemia by constitutive activation of nuclear factor kappa B. Ascorbic acid (AA) is an essential nutrient that possess anti-proliferative and pro-apoptotic activity against a number of malignant cell lines. This study delineates the effect of AA on Tax protein expression as well as NF-κB and MMP9 activity in two HTLV1-positive leukemia cells (HuT-102 and C91-PL). Methods: The cytotoxic and antiproliferative effect of AA were studied by LDH release and MTT tests, respectively. The proteins expression level was assessed by western blotting. RT-PCR was used to study mRNAs level. Finally, ELISA/EMSA and Zymography were used to evaluate NF-κB and MMP-9 activities, respectively. Results: Cell lines were treated with non-cytotoxic concentrations of AA for 48h and 96h, which resulted in a significant inhibition of proliferation at a concentration of 50μg/ml at 96h in both cell lines. The same concentration inhibited Tax protein expression as well as the NF-κB nuclearization and DNA binding activity. The inhibitory effect of AA on MMP9 protein expression and activity started at 100μg/ml and 50μg/ml in HuT-102 and C91-PL cells respectively, with no effect at the transcriptional levels of MMP-9 in either one of the two cell lines. Conclusion: These results indicated that while AA exerted its anti-proliferative effect on the NF-κB activation pathway by suppressing Tax expression, its effects on MMP9 seemed to be independent of this mechanism and follow a different approach. © 2018 Bentham Science Publishers.
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Acute t-cell leukemia, Antipoliferative effect, Ascorbic acid (aa), Human t-cell lymphotrophic virus type i (htlv1), Matrix metalloproteinase-9 (mmp-9), Nf-κb pathway, Tax, Ascorbic acid, Gelatinase b, Immunoglobulin enhancer binding protein, Lactate dehydrogenase, Messenger rna, Tax protein, Antiproliferative activity, Article, Cell proliferation, Controlled study, Cytotoxicity, Enzyme linked immunosorbent assay, Gel mobility shift assay, Human, Human cell, Human t-lymphotropic virus 1, Mtt assay, Protein expression, Reverse transcription polymerase chain reaction, T lymphocyte, Western blotting, Zymography