Combination of Methotrexate and Resveratrol Reduces Pro-Inflammatory Chemokines in Human THP-1 Cells

被引:0
|
作者
Al-Nasser, Moonerah M. [1 ]
Al-Saeedi, Mashael J. [2 ]
Alhowaiti, Saltana A. [2 ]
Shinwari, Zakia [3 ]
Alhamlan, Fatimah S. [2 ,4 ]
Alothaid, Hani [5 ]
Alkahtani, Saad [1 ]
Al-Qahtani, Ahmed A. [2 ,4 ]
机构
[1] King Saud Univ, Coll Sci, Dept Zool, Riyadh, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Res Ctr, Dept Infect & Immun, Riyadh, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Stem Cell & Tissue Reengn Program, Therapeut & Biomarker Discovery Clin Applicat, Riyadh, Saudi Arabia
[4] Alfaisal Univ, Coll Med, Dept Microbiol & Immunol, Riyadh, Saudi Arabia
[5] Al Baha Univ, Fac Appl Med Sci, Dept Basic Sci, Al Baha, Saudi Arabia
关键词
immunomodulatory; immune cells; anti-inflammatory; THP-1; methotrexate; resveratrol; TUMOR-ASSOCIATED MACROPHAGES; INDUCED RENAL DAMAGE; POPULATIONS; PROGRESSION; ADENOSINE; RESPONSES; DISEASE;
D O I
10.2147/JIR.S482503
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Methotrexate (MTX) is a widely used anti-metabolite drug in cancer therapy, but its efficacy is often hindered by reactive oxygen species (ROS)-induced cellular toxicity. Resveratrol, a natural polyphenol, possesses antioxidant and anticancer properties. Therefore, this in vitro study aimed to investigate the synergistic anti-proliferative and anti-inflammatory effects of MTX and resveratrol in human THP-1 cells. Methods: THP-1 cells were differentiated into macrophage-like cells using phorbol 12-myristate 13-acetate. In vitro experiments assessed the impact of various concentrations of MTX and resveratrol on cell viability and proliferation using the MTT assay. Concentration-effect curves were generated to elucidate their relationship. Gene expression was analyzed by RT-qPCR, while chemokine expression was measured via ELISA. Phagocytic and migratory activities were also evaluated. Results: Differentiated THP-1 cells were treated with MTX and resveratrol and stimulated with dimethyl sulfoxide (DMSO) and lipopolysaccharide (LPS) as inflammatory stimuli. The combination of MTX and resveratrol exhibited an anti-proliferative effect in THP-1 cells (p = 0.03). The concentration-effect curve revealed IC50 values of 49.15 mu g at 24 hours (R = 0.8236) and 2.029e-005 mu g at 48 hours (R = 0.97) for MTX, and 20.17 mu g at 48 hours (R = 1.000) and 55.38 mu g at 96 hours (R = 0.9666) for resveratrol. Co-treatment with MTX and resveratrol significantly reduced mRNA and chemokine expression of CCL2, CCL3, CCL4, CCL5, and CXCL10 (p < 0.05). Moreover, decreased phagocytic and migratory activities were confirmed by phagocytosis and migration assays (p < 0.05). Conclusion: The combination of MTX and resveratrol effectively attenuated pro-inflammatory activity in THP-1 cells, as evidenced by the downregulation of mRNA and chemokine expression. These findings suggest that the synergistic effects of MTX and resveratrol hold promise for enhancing cancer therapeutics.
引用
收藏
页码:8085 / 8098
页数:14
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