Linked Life Data

21156787

Source:http://linkedlifedata.com/resource/pubmed/id/21156787

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2011-1-18
pubmed:abstractText
The tyrosine kinase c-Src is upregulated in various human cancers, although the precise regulatory mechanism underlying this upregulation is unclear. We previously reported that a transmembrane adaptor Csk-binding protein (Cbp; PAG1) plays an important role in controlling the cell transformation that is induced by the activation of c-Src. To elucidate the in vivo role of Cbp, we examined the function of Cbp in lung cancer cell lines and tissues. In this study, we found that Cbp was markedly downregulated in human non-small cell lung cancer (NSCLC) cells. The ectopic expression of Cbp suppressed the anchorage-independent growth of the NSCLC cell lines (A549 and Lu99) that had upregulated c-Src, whereas the Cbp expression had little effect on other NSCLC cell lines (PC9 and Lu65) that express normal levels of c-Src. The expression of Cbp suppressed the kinase activity of c-Src in A549 cells by recruiting c-Src and its negative regulator, C-terminal Src kinase (Csk), to lipid rafts. The treatment with Src inhibitors, such as PP2, dasatinib, and saracatinib, also suppressed the growth of A549 cells. Furthermore, Cbp expression attenuated the ability of A549 cells to form tumors in nude mice, invade in vitro, and metastasize in vivo. In addition, we found a significant inverse correlation between the level of Cbp expression and the extent of lymph node metastasis in human lung cancers. These results indicate that Cbp is required for the Csk-mediated inactivation of c-Src and may control the promotion of malignancy in NSCLC tumors that are characterized by c-Src upregulation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1557-3125
pubmed:author
pubmed:copyrightInfo
©2010 AACR.
pubmed:issnType
Electronic
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
103-14
pubmed:dateRevised
2011-11-2
pubmed:meshHeading
pubmed-meshheading:21156787-Adaptor Proteins, Signal Transducing, pubmed-meshheading:21156787-Animals, pubmed-meshheading:21156787-Blotting, Western, pubmed-meshheading:21156787-Carcinoma, Non-Small-Cell Lung, pubmed-meshheading:21156787-Cell Line, Tumor, pubmed-meshheading:21156787-Cell Proliferation, pubmed-meshheading:21156787-Down-Regulation, pubmed-meshheading:21156787-Female, pubmed-meshheading:21156787-Gene Expression Regulation, Neoplastic, pubmed-meshheading:21156787-Humans, pubmed-meshheading:21156787-Lung Neoplasms, pubmed-meshheading:21156787-Membrane Proteins, pubmed-meshheading:21156787-Mice, pubmed-meshheading:21156787-Mice, Inbred BALB C, pubmed-meshheading:21156787-Mice, Nude, pubmed-meshheading:21156787-Neoplasm Metastasis, pubmed-meshheading:21156787-Neoplasms, Experimental, pubmed-meshheading:21156787-Protein Binding, pubmed-meshheading:21156787-Protein-Tyrosine Kinases, pubmed-meshheading:21156787-Proto-Oncogene Proteins, pubmed-meshheading:21156787-Proto-Oncogene Proteins pp60(c-src), pubmed-meshheading:21156787-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:21156787-Transplantation, Heterologous, pubmed-meshheading:21156787-Tumor Burden, pubmed-meshheading:21156787-Up-Regulation
pubmed:year
2011
pubmed:articleTitle
The transmembrane adaptor Cbp/PAG1 controls the malignant potential of human non-small cell lung cancers that have c-src upregulation.
pubmed:affiliation
Department of Oncogene Research, Research Institute for Microbial Diseases, Osaka University. 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't