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Group I p21-activated kinases regulate thyroid cancer cell migration and are overexpressed and activated in thyroid cancer invasion

Authors :
McCarty SK
Saji M
Zhang X
Jarjoura D
Fusco A
Vasko VV
Ringel MD.
Source :
Endocrine-related cancer 17 (2010): 989–999., info:cnr-pdr/source/autori:McCarty SK, Saji M, Zhang X, Jarjoura D, Fusco A, Vasko VV, Ringel MD./titolo:Group I p21-activated kinases regulate thyroid cancer cell migration and are overexpressed and activated in thyroid cancer invasion./doi:/rivista:Endocrine-related cancer/anno:2010/pagina_da:989/pagina_a:999/intervallo_pagine:989–999/volume:17
Publication Year :
2010
Publisher :
BioScientifica, Bristol , Regno Unito, 2010.

Abstract

p21-activated kinases (PAKs) are a family of serine/threonine kinases that regulate cytoskeletal dynamics and cell motility. PAKs are subdivided into group I (PAKs 1-3) and group II (PAKs 4-6) on the basis of structural and functional characteristics. Based on prior gene expression data that predicted enhanced PAK signaling in the invasive fronts of aggressive papillary thyroid cancers (PTCs), we hypothesized that PAKs functionally regulate thyroid cancer cell motility and are activated in PTC invasive fronts. We examined PAK isoform expression in six human thyroid cancer cell lines (BCPAP, KTC1, TPC1, FTC133, C643, and SW1746) by quantitative reverse transcription-PCR and western blot. All cell lines expressed PAKs 1-4 and PAK6 mRNA and PAKs 1-4 protein; PAK6 protein was variably expressed. Samples from normal and malignant thyroid tissues also expressed PAKs 1-4 and PAK6 mRNA; transfection with the group I (PAKs 1-3) PAK-specific p21 inhibitory domain molecular inhibitor reduced transwell filter migration by

Details

Database :
OpenAIRE
Journal :
Endocrine-related cancer 17 (2010): 989–999., info:cnr-pdr/source/autori:McCarty SK, Saji M, Zhang X, Jarjoura D, Fusco A, Vasko VV, Ringel MD./titolo:Group I p21-activated kinases regulate thyroid cancer cell migration and are overexpressed and activated in thyroid cancer invasion./doi:/rivista:Endocrine-related cancer/anno:2010/pagina_da:989/pagina_a:999/intervallo_pagine:989–999/volume:17
Accession number :
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