dc.contributor.author |
Harakeh, Steve Mustapha |
dc.contributor.author |
Khalife, Jihane C. |
dc.contributor.author |
Baydoun, Elias Abdel Hasan |
dc.contributor.author |
Azar, Rania |
dc.contributor.author |
Al-Hejin, Ahmed M. |
dc.contributor.author |
Barbour, Elie K. |
dc.contributor.author |
Azhar, Esam Ibraheem |
dc.contributor.author |
Niedzwiecki, Aleksandra |
dc.contributor.author |
Al-Jaouni, Soad K. |
dc.contributor.author |
Diab-Assaf, Mona |
dc.contributor.author |
Kamal, Mohammad Amjad |
dc.contributor.author |
Rath, Matthias |
dc.date.accessioned |
2025-01-24T11:20:42Z |
dc.date.available |
2025-01-24T11:20:42Z |
dc.date.issued |
2018 |
dc.identifier.uri |
http://hdl.handle.net/10938/25103 |
dc.description.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. |
dc.language.iso |
en |
dc.publisher |
Bentham Science Publishers B.V. |
dc.relation.ispartof |
Anti-Cancer Agents in Medicinal Chemistry |
dc.source |
Scopus |
dc.subject |
Acute t-cell leukemia |
dc.subject |
Antipoliferative effect |
dc.subject |
Ascorbic acid (aa) |
dc.subject |
Human t-cell lymphotrophic virus type i (htlv1) |
dc.subject |
Matrix metalloproteinase-9 (mmp-9) |
dc.subject |
Nf-κb pathway |
dc.subject |
Tax |
dc.subject |
Ascorbic acid |
dc.subject |
Gelatinase b |
dc.subject |
Immunoglobulin enhancer binding protein |
dc.subject |
Lactate dehydrogenase |
dc.subject |
Messenger rna |
dc.subject |
Tax protein |
dc.subject |
Antiproliferative activity |
dc.subject |
Article |
dc.subject |
Cell proliferation |
dc.subject |
Controlled study |
dc.subject |
Cytotoxicity |
dc.subject |
Enzyme linked immunosorbent assay |
dc.subject |
Gel mobility shift assay |
dc.subject |
Human |
dc.subject |
Human cell |
dc.subject |
Human t-lymphotropic virus 1 |
dc.subject |
Mtt assay |
dc.subject |
Protein expression |
dc.subject |
Reverse transcription polymerase chain reaction |
dc.subject |
T lymphocyte |
dc.subject |
Western blotting |
dc.subject |
Zymography |
dc.title |
Effects of ascorbic acid on tax, NF-κB and MMP-9 in human T-cell lymphotropic virus type 1 positive malignant T-lymphocytes |
dc.type |
Article |
dc.contributor.department |
Department of Biology |
dc.contributor.department |
Department of Agriculture |
dc.contributor.faculty |
Faculty of Arts and Sciences (FAS) |
dc.contributor.faculty |
Faculty of Agricultural and Food Sciences (FAFS) |
dc.contributor.institution |
American University of Beirut |
dc.identifier.doi |
https://doi.org/10.2174/1871520617666170725160628 |
dc.identifier.pmid |
28745235 |
dc.identifier.eid |
2-s2.0-85047607044 |