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Cancer cell gene expression modulated from plasma membrane integrin αvβ3 by thyroid hormone and nanoparticulate tetrac.

Authors :
Davis, Paul J.
Glinsky, Gennadi V.
Hung-Yun Lin
Leith, John T.
Hercbergs, Aleck
Heng-Yuan Tang
Ashur-Fabian, Osnat
Incerpi, Sandra
Mousa, Shaker A.
Source :
Frontiers in Endocrinology; Jan2015, Vol. 5, p1-7, 7p
Publication Year :
2015

Abstract

Integrin αvβ3 is generously expressed by cancer cells and rapidly dividing endothelial cells. The principal ligands of the integrin are extracellular matrix proteins, but we have described a cell surface small molecule receptor on αvβ3 that specifically binds thyroid hormone and thyroid hormone analogs. From this receptor, thyroid hormone (L-thyroxine, T<subscript>4</subscript>; 3,5,30-triiodo-L-thyronine, T<subscript>3</subscript>) and tetraiodothyroacetic acid (tetrac) regulate expression of specific genes by a mechanism that is initiated non-genomically. At the integrin, T<subscript>4</subscript> and T<subscript>3</subscript> at physiological concentrations are pro-angiogenic by multiple mechanisms that include gene expression, and T<subscript>4</subscript> supports tumor cell proliferation. Tetrac blocks the transcriptional activities directed by T<subscript>4</subscript> and T<subscript>3</subscript> at αvβ3, but, independently of T<subscript>4</subscript> and T<subscript>3</subscript>, tetrac modulates transcription of cancer cell genes that are important to cell survival pathways, control of the cell cycle, angiogenesis, apoptosis, cell export of chemotherapeutic agents, and repair of double-strand DNA breaks. We have covalently bound tetrac to a 200nm biodegradable nanoparticle that prohibits cell entry of tetrac and limits its action to the hormone receptor on the extracellular domain of plasma membrane αvβ3. This reformulation has greater potency than unmodified tetrac at the integrin and affects a broader range of cancerrelevant genes. In addition to these actions on intra-cellular kinase-mediated regulation of gene expression, hormone analogs at αvβ3 have additional effects on intra-cellular proteintrafficking (cytosol compartment to nucleus), nucleoprotein phosphorylation, and generation of nuclear coactivator complexes that are relevant to traditional genomic actions of T<subscript>3</subscript>. Thus, previously unrecognized cell surface-initiated actions of thyroid hormone and tetrac formulations at αvβ3 offer opportunities to regulate angiogenesis and multiple aspects of cancer cell behavior. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16642392
Volume :
5
Database :
Complementary Index
Journal :
Frontiers in Endocrinology
Publication Type :
Academic Journal
Accession number :
101707221
Full Text :
https://doi.org/10.3389/fendo.2014.00240