KMID : 0381120200420050543
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Genes and Genomics 2020 Volume.42 No. 5 p.543 ~ p.551
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NF-¥êB p65 represses microRNA-124 transcription in diffuse large B-cell lymphoma
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Shim Hye-In
Nam Je-Hyun Kim Sang-Woo
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Abstract
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Background: Previous studies have shown that the copy number of microRNA (miR)-124 is decreased in diffuse large B cell lymphoma (DLBCL), and that miR-124 is a tumor suppressor by targeting NF-¥êB p65 in B-cell lymphoma. In turn, miR-124 expression is regulated by transcription factors such as HNF4¥á, ETS2, and p53. However, whether and how miR-124 transcription is modulated by NF-¥êB transcription factors remain unknown in DLBCL.
Objective: To investigate whether the activation of NF-¥êB signaling could inhibit the expression of miR-124, possibly contributing to the pathogenesis of DLBCL.
Methods: Potential transcription factors regulating miR-124 transcription were predicted using the Transfac software. The cellular effects of NF-¥êB p65 on miR-124 were examined by MTS assay, Western blot assay, qPCR, and chromatin immunoprecipitation (ChIP) assays using DLBCL cell lines.
Results: Inhibition of NF-¥êB signals using Bay11-7085 increased miR-124 expression whereas exposure to TNF-¥á decreased it. Ectopic expression of p65 suppressed miR-124 expression, suggesting that p65 may be a transcriptional repressor of miRNA-124. Pharmacological analyses showed that phosphorylated/activated p65 downregulates miR-124 via two signaling pathways: (1) TAK1/IKK¥á-IKK¥â/I¥êB¥á and (2) MAPK/p65. Moreover, ChIP assay demonstrated that p65 directly regulates miR-124 by binding to the NF-¥êB consensus sequence in its promoter region. Finally, we also confirmed that stable ectopic expression of miR-124 suppresses cell proliferation and survival.
Conclusion: Taken together, our study uncovered a mechanism by which active NF-¥êB signaling disrupts the function of miR-124 as a tumor suppressor in DLBCL.
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KEYWORD
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NF-¥êB p65, miR-124, TAK1, MAPK, DLBCL
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