Patel Prabhudas S, Varney Michelle L, Dave Bhavana J, Singh Rakesh K
Department of Pathology and Microbiology, The University of Nebraska Medical Center, Omaha, NE 68198-7660, USA.
J Interferon Cytokine Res. 2002 Apr;22(4):427-35. doi: 10.1089/10799900252952217.
In the present study, we demonstrate that upregulation of interleukin-1beta(IL-1beta)-mediated and tumor necrosis factor-alpha (TNF-alpha)-mediated IL-8 expression in human malignant melanoma cells is modulated by the activation of nuclear factor-kappaB (NF-kappaB). Addition of capsaicin (8-methyl-N-vanillyl-6-nonenamide), a known inhibitor of NF-kappaB, resulted in the inhibition of constitutive as well as IL-1beta-induced and TNF-alpha-induced IL-8 expression in melanoma cells. The inhibition of IL-8 expression was dependent on the concentration of capsaicin and duration of treatment. Further, electrophoretic mobility shift assay (EMSA) of nuclear extracts from melanoma cells showed a constitutive activation of NF-kappaB and activated protein 1 (AP-1), which was upregulated following treatment with IL-1beta. Treatment of melanoma cells with capsaicin inhibited activation of constitutive and IL-1beta-induced NF-kappaB, but not AP-1, leading to inhibition of IL-8 expression. Further, downregulation of IL-8 expression in capsaicin-treated melanoma cells resulted in inhibition of in vitro cell proliferation. These results demonstrate that constitutive and induced NF-kappaB activation regulates IL-8 expression in melanoma cells. Downregulation of constitutive and induced NF-kappaB activation in malignant melanoma cells leads to inhibition of IL-8 production and in vitro cell proliferation.
在本研究中,我们证明了人恶性黑色素瘤细胞中白细胞介素-1β(IL-1β)介导的和肿瘤坏死因子-α(TNF-α)介导的IL-8表达上调是由核因子-κB(NF-κB)的激活所调节的。添加辣椒素(8-甲基-N-香草基-6-壬酰胺),一种已知的NF-κB抑制剂,导致黑色素瘤细胞中组成性以及IL-1β诱导和TNF-α诱导的IL-8表达受到抑制。IL-8表达的抑制取决于辣椒素的浓度和处理时间。此外,对黑色素瘤细胞核提取物进行的电泳迁移率变动分析(EMSA)显示NF-κB和活化蛋白1(AP-1)的组成性激活,在用IL-1β处理后其活性上调。用辣椒素处理黑色素瘤细胞可抑制组成性和IL-1β诱导的NF-κB的激活,但不抑制AP-1的激活,从而导致IL-8表达受到抑制。此外,辣椒素处理的黑色素瘤细胞中IL-8表达的下调导致体外细胞增殖受到抑制。这些结果表明,组成性和诱导性NF-κB激活调节黑色素瘤细胞中IL-8的表达。恶性黑色素瘤细胞中组成性和诱导性NF-κB激活的下调导致IL-8产生和体外细胞增殖受到抑制。