Thyroid hormone receptor β1 domains responsible for the antagonism with the ras oncogene: role of corepressors (Q64460314)

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15 February 2020

title

Thyroid hormone receptor β1 domains responsible for the antagonism with the ras oncogene: role of corepressors (English)

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1

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author name string

O Martínez-Iglesias

series ordinal

2

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L Ruiz-Llorente

series ordinal

3

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A Aranda

series ordinal

4

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language of work or name

English

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publication date

18 October 2010

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15 February 2020

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volume

30

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issue

7

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page(s)

854-864

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https://scigraph.springernature.com/pub.10.1038/onc.2010.464

15 February 2020

exact match

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cites work

The RSK family of kinases: emerging roles in cellular signalling

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Nuclear hormone receptors and gene expression

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Thyroid receptor: roles in cancer.

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Corepressor SMRT functions as a coactivator for thyroid hormone receptor T3Ralpha from a negative hormone response element

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Increasing complexity of Ras signaling.

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A permissive retinoid X receptor/thyroid hormone receptor heterodimer allows stimulation of prolactin gene transcription by thyroid hormone and 9-cis-retinoic acid

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Thyroid hormone receptors mutated in liver cancer function as distorted antimorphs

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Selective transrepression versus transactivation mechanisms by glucocorticoid receptor modulators in stress and immune systems

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Hormone-dependent coactivator binding to a hydrophobic cleft on nuclear receptors

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Aberrant cytoplasmic localization of N-CoR in colorectal tumors

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International Union of Pharmacology. LIX. The pharmacology and classification of the nuclear receptor superfamily: thyroid hormone receptors

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An unliganded thyroid hormone beta receptor activates the cyclin D1/cyclin-dependent kinase/retinoblastoma/E2F pathway and induces pituitary tumorigenesis

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Nongenomic activation of phosphatidylinositol 3-kinase signaling by thyroid hormone receptors

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The thyroid hormone receptor is a suppressor of ras-mediated transcription, proliferation, and transformation

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Arsenic trioxide is a potent inhibitor of the interaction of SMRT corepressor with Its transcription factor partners, including the PML-retinoic acid receptor alpha oncoprotein found in human acute promyelocytic leukemia

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Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor

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Activation of mitogen-activated protein kinases/extracellular signal-regulated kinases in human hepatocellular carcinoma

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Diverse signaling pathways modulate nuclear receptor recruitment of N-CoR and SMRT complexes

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Nuclear receptor corepressors

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Ras transformation results in an elevated level of cyclin D1 and acceleration of G1 progression in NIH 3T3 cells

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Function and regulation of ras.

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Thyroid hormone receptor beta1 acts as a potent suppressor of tumor invasiveness and metastasis

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Hypothyroidism enhances tumor invasiveness and metastasis development

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The thyroid hormone receptor antagonizes CREB-mediated transcription

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Nuclear receptors versus inflammation: mechanisms of transrepression

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Molecular determinants of nuclear receptor-corepressor interaction

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The silencing mediator of retinoic acid and thyroid hormone receptor (SMRT) corepressor is required for full estrogen receptor alpha transcriptional activity

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Dynamic stabilization of nuclear receptor ligand binding domains by hormone or corepressor binding

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The role of corepressors in transcriptional regulation by nuclear hormone receptors

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Reduced skin tumor development in cyclin D1-deficient mice highlights the oncogenic ras pathway in vivo

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Factor recruitment and TIF2/GRIP1 corepressor activity at a collagenase-3 response element that mediates regulation by phorbol esters and hormones

31 March 2020

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Defective release of corepressor by hinge mutants of the thyroid hormone receptor found in patients with resistance to thyroid hormone.

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The retinoid X receptor ligand restores defective signalling by the vitamin D receptor

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Alteration of SMRT tumor suppressor function in transformed non-Hodgkin lymphomas

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Mice with a mutation in the thyroid hormone receptor beta gene spontaneously develop thyroid carcinoma: a mouse model of thyroid carcinogenesis.

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Nuclear receptor corepressors activate rather than suppress basal transcription of genes that are negatively regulated by thyroid hormone

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Coupling of the RAS-MAPK pathway to gene activation by RSK2, a growth factor-regulated CREB kinase

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Physiological and molecular basis of thyroid hormone action

31 March 2020

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Thyroid hormone receptors are tumor suppressors in a mouse model of metastatic follicular thyroid carcinoma

31 March 2020

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31 March 2020

Identifiers

DOI

10.1038/ONC.2010.464

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20956942%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

15 February 2020

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1 reference