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rdf:type |
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lifeskim:mentions |
umls-concept:C0009452,
umls-concept:C0013879,
umls-concept:C0018270,
umls-concept:C0025202,
umls-concept:C0061928,
umls-concept:C0205144,
umls-concept:C0314603,
umls-concept:C1269955,
umls-concept:C1517945,
umls-concept:C2003905,
umls-concept:C2699153
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pubmed:issue |
34
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pubmed:dateCreated |
2001-8-10
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pubmed:abstractText |
Normal human melanocytes are interspersed singly among keratinocytes along the basement membrane of the epidermis, whereas melanoma cells readily adhere to each other during invasion of the dermis or distant organs. The tumorigenic and metastatic phenotype of melanoma cells often correlates with increased expression of cell-cell and cell-matrix adhesion receptors. Mel-CAM (MCAM, MUC 18, CD146) is a cell-cell adhesion receptor highly expressed by melanoma cells but not normal melanocytes. We show here that inhibition of Mel-CAM expression in metastatic melanoma cells using genetic suppressor elements of Mel-CAM cDNA leads to inhibition of adhesion between melanoma cells and to downregulation of the tumorigenic phenotype. Growth was not inhibited in genetic suppressor elements-transduced melanoma cells cultured in monolayers but was inhibited when cells were maintained anchorage-independently in soft agar and greatly reduced in immunodeficient mice. A three-dimensional epidermal skin equivalent model demonstrated that Mel-CAM allows melanoma cells to separate from the epidermis and invade the basement membrane zone and dermis. However, melanoma cells with little or no Mel-CAM were poorly invasive, possibly due to their loss of gap junctional communication. These results suggest the multifunctional role of a melanoma-associated cell-cell adhesion receptor in tumor progression.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD146,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Surface,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Antisense,
http://linkedlifedata.com/resource/pubmed/chemical/MCAM protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Mcam protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Neural Cell Adhesion Molecules
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0950-9232
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:day |
2
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4676-84
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11498790-Animals,
pubmed-meshheading:11498790-Antigens, CD,
pubmed-meshheading:11498790-Antigens, CD146,
pubmed-meshheading:11498790-Antigens, Surface,
pubmed-meshheading:11498790-Apoptosis,
pubmed-meshheading:11498790-Cell Adhesion,
pubmed-meshheading:11498790-Cell Communication,
pubmed-meshheading:11498790-Cell Division,
pubmed-meshheading:11498790-Cells, Cultured,
pubmed-meshheading:11498790-DNA, Antisense,
pubmed-meshheading:11498790-Down-Regulation,
pubmed-meshheading:11498790-Gap Junctions,
pubmed-meshheading:11498790-Humans,
pubmed-meshheading:11498790-Melanoma,
pubmed-meshheading:11498790-Membrane Glycoproteins,
pubmed-meshheading:11498790-Mice,
pubmed-meshheading:11498790-Mice, SCID,
pubmed-meshheading:11498790-Neoplasm Invasiveness,
pubmed-meshheading:11498790-Neural Cell Adhesion Molecules,
pubmed-meshheading:11498790-Skin,
pubmed-meshheading:11498790-Tumor Cells, Cultured
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pubmed:year |
2001
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pubmed:articleTitle |
Mel-CAM-specific genetic suppressor elements inhibit melanoma growth and invasion through loss of gap junctional communication.
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pubmed:affiliation |
The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania, PA 19104 USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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