rdf:type |
|
lifeskim:mentions |
umls-concept:C0007112,
umls-concept:C0017262,
umls-concept:C0025914,
umls-concept:C0026336,
umls-concept:C0026809,
umls-concept:C0036525,
umls-concept:C0185117,
umls-concept:C0205217,
umls-concept:C0217846,
umls-concept:C0449258,
umls-concept:C1334487,
umls-concept:C1412371,
umls-concept:C1522484,
umls-concept:C2911684
|
pubmed:issue |
5
|
pubmed:dateCreated |
2005-4-11
|
pubmed:abstractText |
The transgenic adenocarcinoma mouse prostate (TRAMP) model is a paradigm that closely mimics the progression of clinical prostate cancer. We have previously reported that MUC18, a cell adhesion molecule in the Ig gene superfamily, is a marker as well as an important mediator for the metastatic potential of human prostate cancer cells. In this study we investigated the possible correlation of increased MUC18 expression with the malignant progression of prostate cancer in the TRAMP model.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0022-5347
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
173
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1778-83
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:15821586-Adenocarcinoma,
pubmed-meshheading:15821586-Animals,
pubmed-meshheading:15821586-Antigens, CD,
pubmed-meshheading:15821586-Antigens, CD146,
pubmed-meshheading:15821586-Disease Progression,
pubmed-meshheading:15821586-Male,
pubmed-meshheading:15821586-Mice,
pubmed-meshheading:15821586-Mice, Inbred C57BL,
pubmed-meshheading:15821586-Mice, Transgenic,
pubmed-meshheading:15821586-Neural Cell Adhesion Molecules,
pubmed-meshheading:15821586-Prostatic Neoplasms,
pubmed-meshheading:15821586-Tumor Markers, Biological
|
pubmed:year |
2005
|
pubmed:articleTitle |
Increased expression of MUC18 correlates with the metastatic progression of mouse prostate adenocarcinoma in the TRAMP model.
|
pubmed:affiliation |
Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322, USA. wu@microbio.emory.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
|