Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2007-1-3
pubmed:abstractText
Valosin-containing protein (VCP) is involved in a wide variety of cellular functions. Our previous studies showed that the enhanced expression of VCP in cancer cells correlated with invasion and metastasis of cancers. Here, the regulatory mechanism for VCP transcription was investigated. Luciferase reporter constructs containing serially deleted 5'-flanking region of the VCP gene were transfected into MCF7 mammary carcinoma cell line, in which VCP was abundantly expressed. The deletion and mutation at the two binding motifs for pre-B-cell leukemia transcription factor 1 (PBX1) reduced the luciferase activity, indicating that these two PBX1 motifs mediated the transactivation of the VCP gene. Chromatin immunoprecipitation assay showed the binding of PBX-1 to the 5'-flanking region of the VCP gene. The knockdown of PBX1 by siRNA decreased the expression level of VCP. VCP is reported to maintain cell viability after the treatment of tumor necrosis factor-alpha. The viability of tumor necrosis factor-alpha-treated cells was significantly reduced in PBX1 knockdown MCF7. These findings indicate that PBX1 plays a crucial role in VCP expression and function and that the PBX-VCP pathway might be important for cell survival under cytokine stress.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-10187799, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-10682845, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-11010815, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-11163219, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-11483959, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-11927012, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-12351637, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-12560433, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-12724421, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-12829673, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-12847084, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-14760088, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-14761919, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-15034582, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-15037236, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-15131036, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-15149596, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-15177017, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-15231524, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-15328197, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-1672117, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-1967982, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-1967983, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-2140770, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-7553849, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-7791786, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-8093327, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-8104101, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-9452483, http://linkedlifedata.com/resource/pubmed/commentcorrection/17200190-9639875
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0002-9440
pubmed:author
pubmed:issnType
Print
pubmed:volume
170
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
152-9
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:17200190-5' Flanking Region, pubmed-meshheading:17200190-Adenosine Triphosphatases, pubmed-meshheading:17200190-Cell Cycle Proteins, pubmed-meshheading:17200190-Cell Line, Tumor, pubmed-meshheading:17200190-Cell Survival, pubmed-meshheading:17200190-DNA-Binding Proteins, pubmed-meshheading:17200190-Female, pubmed-meshheading:17200190-Gene Expression Regulation, Neoplastic, pubmed-meshheading:17200190-Humans, pubmed-meshheading:17200190-Male, pubmed-meshheading:17200190-Mutagenesis, Site-Directed, pubmed-meshheading:17200190-Neoplasms, pubmed-meshheading:17200190-Proto-Oncogene Proteins, pubmed-meshheading:17200190-RNA, Small Interfering, pubmed-meshheading:17200190-Sequence Deletion, pubmed-meshheading:17200190-Signal Transduction, pubmed-meshheading:17200190-Tumor Necrosis Factor-alpha
pubmed:year
2007
pubmed:articleTitle
Pre-B-cell leukemia transcription factor 1 regulates expression of valosin-containing protein, a gene involved in cancer growth.
pubmed:affiliation
Department of Pathology, Medical School of Tongji University, Shanghai, China.
pubmed:publicationType
Journal Article