Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2007-6-4
pubmed:abstractText
MUC1 is a heterodimeric transmembrane glycoprotein that is overexpressed and aberrantly glycosylated in ductal adenocarcinomas. Differential phosphorylation of the MUC1 cytoplasmic tail (MUC1CT) has been associated with signaling events that influence the proliferation and metastasis of cancer cells. We identified a novel tyrosine phosphorylation site (HGRYVPP) in the MUC1CT by mass spectrometric analysis of MUC1 from human pancreatic adenocarcinoma cell lines. Analyses in vitro and in vivo showed that platelet-derived growth factor receptor beta (PDGFRbeta) catalyzed phosphorylation of this site and of tyrosine in the RDTYHPM site. Stimulation of S2-013.MUC1F cells with PDGF-BB increased nuclear colocalization of MUC1CT and beta-catenin. PDGF-BB stimulation had no significant effect on cell proliferation rate; however, it enhanced invasion in vitro through Matrigel and in vivo tumor growth and metastases. Invasive properties of the cells were significantly altered on expression of phosphorylation-abrogating or phosphorylation-mimicking mutations at these sites. We propose that interactions of MUC1 and PDGFRbeta induce signal transduction events that influence the metastatic properties of pancreatic adenocarcinoma.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0008-5472
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
67
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5201-10
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17545600-Adenocarcinoma, pubmed-meshheading:17545600-Amino Acid Motifs, pubmed-meshheading:17545600-Amino Acid Sequence, pubmed-meshheading:17545600-Animals, pubmed-meshheading:17545600-Antigens, Neoplasm, pubmed-meshheading:17545600-Binding Sites, pubmed-meshheading:17545600-Cell Line, Tumor, pubmed-meshheading:17545600-Cell Nucleus, pubmed-meshheading:17545600-Female, pubmed-meshheading:17545600-Humans, pubmed-meshheading:17545600-Mass Spectrometry, pubmed-meshheading:17545600-Mice, pubmed-meshheading:17545600-Mice, Nude, pubmed-meshheading:17545600-Molecular Sequence Data, pubmed-meshheading:17545600-Mucin-1, pubmed-meshheading:17545600-Mucins, pubmed-meshheading:17545600-Neoplasm Invasiveness, pubmed-meshheading:17545600-Pancreatic Neoplasms, pubmed-meshheading:17545600-Phosphorylation, pubmed-meshheading:17545600-Receptor, Platelet-Derived Growth Factor beta, pubmed-meshheading:17545600-Tyrosine, pubmed-meshheading:17545600-beta Catenin
pubmed:year
2007
pubmed:articleTitle
Platelet-derived growth factor receptor beta-mediated phosphorylation of MUC1 enhances invasiveness in pancreatic adenocarcinoma cells.
pubmed:affiliation
Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska 68198-6805, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural