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rdf:type |
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lifeskim:mentions |
umls-concept:C0001271,
umls-concept:C0017262,
umls-concept:C0185117,
umls-concept:C0221908,
umls-concept:C1154398,
umls-concept:C1412810,
umls-concept:C1417607,
umls-concept:C1423773,
umls-concept:C1512505,
umls-concept:C1824986,
umls-concept:C2911684
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pubmed:issue |
3
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pubmed:dateCreated |
2010-1-14
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pubmed:abstractText |
DUOXA1/NIP1, originally identified as a Numb-interacting protein, was recently shown to function as a maturation factor for the dual oxidase 1(DUOX1). In this study, we identified DUOXA1/NIP1 expression in breast cancer cells, observed high expression of DUOXA1 in non-invasive MCF7 cells and low expression in highly metastatic cells with impaired p53 functions linking the expression of DUOXA1 with p53. An inhibition of cell proliferation associated with upregulation of p21(Cip1/WAF1) was observed in MDA-MB-231 cells following transfection of DUOXA1. The transient DUOXA1 overexpression also inhibited expression of cell-surface integrin alphaVbeta5 and CD9, which is associated with impaired spreading ability. However, there was no difference in expression of these proteins in DUOX1-depleted cells. The observed effects coincided with an increase in reactive oxygen species (ROS) generation. Our data also demonstrate that DUOXA1 transient overexpression affected the cell-cell adhesion by modulating the actin cytoskeleton, and sensitized cells to doxorubicin.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1573-7217
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
119
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
773-86
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pubmed:meshHeading |
pubmed-meshheading:19322654-Actins,
pubmed-meshheading:19322654-Blotting, Western,
pubmed-meshheading:19322654-Breast Neoplasms,
pubmed-meshheading:19322654-Cell Adhesion,
pubmed-meshheading:19322654-Cell Line, Tumor,
pubmed-meshheading:19322654-Cell Separation,
pubmed-meshheading:19322654-Cyclin-Dependent Kinase Inhibitor p21,
pubmed-meshheading:19322654-Cytoskeleton,
pubmed-meshheading:19322654-Epithelial Cells,
pubmed-meshheading:19322654-Female,
pubmed-meshheading:19322654-Flow Cytometry,
pubmed-meshheading:19322654-Fluorescent Antibody Technique,
pubmed-meshheading:19322654-Gene Expression,
pubmed-meshheading:19322654-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:19322654-Humans,
pubmed-meshheading:19322654-NADPH Oxidase,
pubmed-meshheading:19322654-Nuclear Cap-Binding Protein Complex,
pubmed-meshheading:19322654-Reactive Oxygen Species,
pubmed-meshheading:19322654-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:19322654-Transfection,
pubmed-meshheading:19322654-Tumor Suppressor Protein p53
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pubmed:year |
2010
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pubmed:articleTitle |
NIP1/DUOXA1 expression in epithelial breast cancer cells: regulation of cell adhesion and actin dynamics.
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pubmed:affiliation |
Department of Biochemistry and Siebens Drake Medical Research Institute, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON N6A 5C1, Canada. eostrakh@uwo.ca
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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