(Q46017171)

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HDAC3 represses the expression of NKG2D ligands ULBPs in epithelial tumour cells: potential implications for the immunosurveillance of cancer.

scientific article published on 11 May 2009

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27 January 2020

HDAC3 represses the expression of NKG2D ligands ULBPs in epithelial tumour cells: potential implications for the immunosurveillance of cancer (English)

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27 January 2020

Alicia R Folgueras

2

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27 January 2020

Segundo González

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27 January 2020

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A López-Soto

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27 January 2020

E Seto

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27 January 2020

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11 May 2009

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27 January 2020

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27 January 2020

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27 January 2020

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27 January 2020

2370-2382

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27 January 2020

https://scigraph.springernature.com/pub.10.1038/onc.2009.117

0 references

Acetylated sp3 is a transcriptional activator

1 reference

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Molecular regulation of MHC class I chain-related protein A expression after HDAC-inhibitor treatment of Jurkat T cells

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Natural killer cell-mediated lysis of hepatoma cells via specific induction of NKG2D ligands by the histone deacetylase inhibitor sodium valproate

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Transcription factor Sp3 is regulated by acetylation

1 reference

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ULBPs, novel MHC class I-related molecules, bind to CMV glycoprotein UL16 and stimulate NK cytotoxicity through the NKG2D receptor

1 reference

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Duration of nuclear NF-kappaB action regulated by reversible acetylation

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NKG2D ligand expression in AML increases in response to HDAC inhibitor valproic acid and contributes to allorecognition by NK-cell lines with single KIR-HLA class I specificities

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Histone deacetylase 1 can repress transcription by binding to Sp1.

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Human HDAC7 histone deacetylase activity is associated with HDAC3 in vivo

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NKG2D ligands: key targets of the immune response.

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Disulphide-isomerase-enabled shedding of tumour-associated NKG2D ligands.

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HDAC3: taking the SMRT-N-CoRrect road to repression

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Regulation of the expression of MHC class I-related chain A, B (MICA, MICB) via chromatin remodeling and its impact on the susceptibility of leukemic cells to the cytotoxicity of NKG2D-expressing cells

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Liver-specific deletion of histone deacetylase 3 disrupts metabolic transcriptional networks

1 reference

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Chromatin modifications and their function

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The NKG2D receptor: sensing stressed cells

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Transcriptional regulation of ULBP1, a human ligand of the NKG2D receptor

1 reference

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Deacetylation of p53 modulates its effect on cell growth and apoptosis

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Epigenetic targets for immune intervention in human malignancies

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Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer

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NKG2D ligands in tumor immunity

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Transforming pathways unleashed by a HDAC2 mutation in human cancer.

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Functional expression and release of ligands for the activating immunoreceptor NKG2D in leukemia

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Sirtuins: critical regulators at the crossroads between cancer and aging

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Cancer cells become susceptible to natural killer cell killing after exposure to histone deacetylase inhibitors due to glycogen synthase kinase-3-dependent expression of MHC class I-related chain A and B.

1 reference

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NKG2D function protects the host from tumor initiation

1 reference

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The transcriptional repressor Sp3 is associated with CK2-phosphorylated histone deacetylase 2

1 reference

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ULBPs, human ligands of the NKG2D receptor, stimulate tumor immunity with enhancement by IL-15.

1 reference

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Class II histone deacetylases: versatile regulators

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NK cells and cancer immunosurveillance.

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Histone deacetylase 3 (HDAC3) and other class I HDACs regulate colon cell maturation and p21 expression and are deregulated in human colon cancer

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Mechanisms of ceramide-mediated repression of the human telomerase reverse transcriptase promoter via deacetylation of Sp3 by histone deacetylase 1

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Histone deacetylase inhibitors activate INK4d gene through Sp1 site in its promoter

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Tumour-derived soluble MIC ligands impair expression of NKG2D and T-cell activation

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Innate immune dysfunction in HIV infection: effect of HIV envelope-NK cell interactions

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