Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1991-3-15
pubmed:abstractText
We have previously shown that expression of the H-ras oncogene alone does not induce progression of a tumorigenic but non-metastatic murine fibroblast cell line (LTA) to a metastatic phenotype. Because myc genes, alone or with ras, have been implicated at different stages of progression in other systems, we examined the ability of v-myc, alone and in combination with H-ras, to induce malignant conversion of LTA. We found no increase in either "spontaneous" (assessed after s.c. injection into nude mice) or "experimental" (assessed after i.v. injection into chick embryos) metastatic ability in spite of high levels of v-myc RNA in LTA cells transfected with v-myc alone. Serial in vivo passaging did not consistently select for either myc expression or metastatic ability. Myc transfected cells expressing high levels of myc RNA were subsequently transfected with H-ras. LTA cells expressing both oncogenes at high levels remained non-metastatic. LTA cells thus are resistant to the effects of myc and ras oncogenes (alone and in combination) on a specific stage of tumor progression, that of malignant conversion, and may offer a good model for studying mechanisms of resistance to these oncogenes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0250-7005
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:geneSymbol
H-ras, v-myc
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1507-14
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:articleTitle
Resistance of murine LTA cells to oncogene--mediated progression from tumorigenic to metastatic phenotype.
pubmed:affiliation
London Regional Cancer Centre, Ontario, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't