Source:http://linkedlifedata.com/resource/pubmed/id/10211981
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
1999-5-6
|
pubmed:abstractText |
CT 26 murine colon carcinoma cells demonstrated directional migration (chemotaxis) in response to fibronectin (FN). Sub-lines were derived by positive and negative selection to FN across Transwell filters of 8 microm pore size. The FL6 sub-line (positively selected) demonstrated a significantly increased chemotactic response (P<0.01) to FN compared with parental CT 26 cells, while the FU7 sub-line (negatively selected) showed a reduced chemotactic response to FN (P<0.01). Comparable levels of alpha4, alpha5, alphav and beta1 integrins, which mediate FN attachment, were expressed on positively and negatively selected sub-lines and parental CT 26 cells. Activation of integrins with Mn2+ suggested that the integrins expressed on FL6 cells were in the fully activated state; in contrast FU7 cells displayed only partially activated integrins. Cell attachment and integrin activation status of the sub-lines correlated with their chemotactic response to FN. In vivo FL6 cells showed a significantly reduced tumour growth rate s.c. and a reduction in the number of lung colonies formed following i.v. injection compared with parental CT 26 and FU7 cells. In contrast FU7 cells displayed a significant increase in s.c. tumour growth and the number of lung colonies when compared with the parental line and FL6 sub-line. The results indicate that interaction between integrin receptors expressed on cancer cells and FN plays a central role in the chemotactic response of CT 26 colon carcinoma cells, and that in this model cells selected for chemotaxis to FN displayed a reduced malignant potential.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chemotactic Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Collagen,
http://linkedlifedata.com/resource/pubmed/chemical/Extracellular Matrix Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Fibronectins,
http://linkedlifedata.com/resource/pubmed/chemical/Laminin
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0262-0898
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
16
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
683-91
|
pubmed:dateRevised |
2003-11-14
|
pubmed:meshHeading |
pubmed-meshheading:10211981-Adenocarcinoma,
pubmed-meshheading:10211981-Animals,
pubmed-meshheading:10211981-Cell Adhesion,
pubmed-meshheading:10211981-Cell Division,
pubmed-meshheading:10211981-Cell Transformation, Neoplastic,
pubmed-meshheading:10211981-Chemotactic Factors,
pubmed-meshheading:10211981-Chemotaxis,
pubmed-meshheading:10211981-Collagen,
pubmed-meshheading:10211981-Colonic Neoplasms,
pubmed-meshheading:10211981-Extracellular Matrix Proteins,
pubmed-meshheading:10211981-Fibronectins,
pubmed-meshheading:10211981-Laminin,
pubmed-meshheading:10211981-Lung Neoplasms,
pubmed-meshheading:10211981-Mice,
pubmed-meshheading:10211981-Tumor Cells, Cultured
|
pubmed:year |
1998
|
pubmed:articleTitle |
Fibronectin is chemotactic for CT 26 colon carcinoma cells: sub-lines selected for increased chemotaxis to fibronectin display decreased tumorigenicity and lung colonization.
|
pubmed:affiliation |
Department of Life Sciences, Nottingham Trent University, UK.
|
pubmed:publicationType |
Journal Article
|