Identification of a novel cell type-specific intronic enhancer of macrophage migration inhibitory factor (MIF) and its regulation by mithramycin. (Q34595260)

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English	Identification of a novel cell type-specific intronic enhancer of macrophage migration inhibitory factor (MIF) and its regulation by mithramycin.	scientific article

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scholarly article

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16 January 2020

Identification of a novel cell type-specific intronic enhancer of macrophage migration inhibitory factor (MIF) and its regulation by mithramycin (English)

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16 January 2020

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16 January 2020

author name string

E Beaulieu

1

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L Green

2

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L Elsby

3

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Z Alourfi

4

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publication date

19 November 2010

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16 January 2020

Clinical and Experimental Immunology

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163

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16 January 2020

2

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178-188

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16 January 2020

Hypoxia and glucocorticoid signaling converge to regulate macrophage migration inhibitory factor gene expression

1 reference

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Sp1: emerging roles--beyond constitutive activation of TATA-less housekeeping genes

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Regulation of constitutive and microbial pathogen-induced human macrophage migration inhibitory factor (MIF) gene expression

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HIF1alpha delays premature senescence through the activation of MIF.

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Human macrophage migration inhibitory factor: a proven immunomodulatory cytokine?

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Macrophage migration inhibitory factor: a mediator of matrix metalloproteinase-2 production in rheumatoid arthritis.

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Dual regulation of macrophage migration inhibitory factor (MIF) expression in hypoxia by CREB and HIF-1.

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Macrophage migration inhibitory factor and glucocorticoid sensitivity.

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Novel GC-rich DNA-binding compound produced by a genetically engineered mutant of the mithramycin producer Streptomyces argillaceus exhibits improved transcriptional repressor activity: implications for cancer therapy.

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Mithramycin A activates Fas death pathway in leukemic cell lines

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Macrophage migration inhibitory factor promotes innate immune responses by suppressing glucocorticoid-induced expression of mitogen-activated protein kinase phosphatase-1.

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Mithramycin downregulates proinflammatory cytokine-induced matrix metalloproteinase gene expression in articular chondrocytes

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Glucocorticoids suppress macrophage migration inhibitory factor (MIF) expression in a cell-type-specific manner.

1 reference

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Nuclear receptor-mediated transactivation through interaction with Sp proteins

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Hypoxia-induced activation of the retinoic acid receptor-related orphan receptor alpha4 gene by an interaction between hypoxia-inducible factor-1 and Sp1.

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Macrophage migration inhibitory factor: a regulator of innate immunity

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Inhibition of c-src transcription by mithramycin: structure-activity relationships of biosynthetically produced mithramycin analogues using the c-src promoter as target

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Novel transcriptional regulation of the human CYP3A7 gene by Sp1 and Sp3 through nuclear factor kappa B-like element

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Transcription of eukaryotic protein-coding genes

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Transcriptional activation of the macrophage migration-inhibitory factor gene by the corticotropin-releasing factor is mediated by the cyclic adenosine 3',5'- monophosphate responsive element-binding protein CREB in pituitary cells

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A pilot study of alpha-interferon and plicamycin for accelerated phase of chronic myeloid leukemia

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Transcription factor Sp1 is essential for early embryonic development but dispensable for cell growth and differentiation

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An essential role for macrophage migration inhibitory factor in the tuberculin delayed-type hypersensitivity reaction

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MIF is a pituitary-derived cytokine that potentiates lethal endotoxaemia

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The macrophage is an important and previously unrecognized source of macrophage migration inhibitory factor

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MIF as a glucocorticoid-induced modulator of cytokine production

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Mithramycin selectively inhibits transcription of G-C containing DNA.

1 reference

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Mithramycin blocks protein binding and function of the SV40 early promoter

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Macrophage migration inhibitory factor up-regulates expression of matrix metalloproteinases in synovial fibroblasts of rheumatoid arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21087445

12 December 2020

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1 reference

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1 reference

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https://pubmed.ncbi.nlm.nih.gov/21087445

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Identifiers

10.1111/J.1365-2249.2010.04289.X

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16 January 2020

1 reference

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16 January 2020

1 reference

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16 January 2020

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