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  4. Taxol reduces cytosolic E-cadherin and β-catenin levels in nasopharyngeal carcinoma cell line TW-039: Cross-talk between the microtubule- and actin-based cytoskeletons
 
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Taxol reduces cytosolic E-cadherin and β-catenin levels in nasopharyngeal carcinoma cell line TW-039: Cross-talk between the microtubule- and actin-based cytoskeletons

Journal
Journal of Cellular Biochemistry
Journal Volume
79
Journal Issue
4
Pages
542-556
Date Issued
2000
Author(s)
PEI-JEN LOU  
WEN-PIN CHEN  orcid-logo
CHIN-TARNG LIN  
Chen H.-C.
Wu J.-C.
DOI
10.1002/1097-4644(20001215)79:4<542
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033788821&doi=10.1002%2f1097-4644%2820001215%2979%3a4%3c542%3a%3aAID-JCB30%3e3.0.CO%3b2-Q&partnerID=40&md5=77db5fc38774ba1a91bfd88d68475c9d
https://scholars.lib.ntu.edu.tw/handle/123456789/518330
Abstract
Taxol affects microtubule dynamics by promoting microtubule assembly. To obtain a better insight into possible cross-talk between the microtubule- and actin-based cytoskeletons, we studied the short-term effects of Taxol treatment on the expression of actin and the E-cadherin/catenin complex in the nasopharyngeal carcinoma cell line TW-039 using immunofluorescence, immunoprecipitation, and immunoblotting methods. Morphologic changes in actin filaments, including ventral actin dumps and perijunctional actin blebs, were seen at Taxol concentrations ?1 μM. Levels of detergent-soluble E-cadherin fell to 53% or 58% compared to controls in cells treated, respectively, with 1 or 5 μM Taxol, while levels of detergent-soluble β-catenin fell to 76% or 74%. Levels of the detergent-soluble pool of α- and γ-catenin and the detergent-insoluble pool of the E-cadherin/catenin complex were unchanged by Taxol treatment and no significant difference was seen in the levels of adenomatous polyposis coli or glycogen synthase-3β or tyrosine phosphorylation patterns. These results suggest that modulation of microtubule dynamics by Taxol may have effects on the expression of actin and the cytosolic E-cadherin and β-catenin in nasopharyngeal carcinoma cells through pathways not involving the phosphorylation of β-catenin. (C) 2000 Wiley-Liss, Inc.
SDGs

[SDGs]SDG3

Other Subjects
actin; beta catenin; paclitaxel; uvomorulin; actin filament; article; cancer cell culture; controlled study; cytosol; drug effect; microtubule assembly; molecular interaction; nasopharynx carcinoma; priority journal; protein phosphorylation; Actins; Adenomatous Polyposis Coli Protein; Antineoplastic Agents, Phytogenic; Ca(2+)-Calmodulin Dependent Protein Kinase; Cadherins; Cell Size; Cytoskeletal Proteins; Cytoskeleton; Cytosol; Human; Microtubules; Nasopharyngeal Neoplasms; Neoplasm Proteins; Paclitaxel; Phosphorylation; Support, Non-U.S. Gov't; Tumor Cells, Cultured; Tyrosine
Type
journal article

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