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Title

Suppression of the metastatic phenotype of a mouse skin carcinoma cell line independent of E-cadherin expression and correlated with reduced levels of Ha-ras oncogene products

AuthorsCaulín, Carlos; Navarro, Pilar ; Lozano, Encarnación ; Rodrigo Castro, M. Isabel; Gamallo, Carlos; Cano, Amparo ; Fabra, Àngels; Quintanilla, Miguel
Issue Date1996
PublisherWiley-Blackwell
CitationMolecular Carcinogenesis 15(2): 104-114 (1996)
AbstractThe HaCa4 cell line, derived from a mouse skin carcinoma induced by Harvey murine sarcoma virus, is highly tumorigenic when injected into nude mice and produces multiple metastases in the lungs. HaCa4 cells express high levels of viral Ha-ras oncogene products, anomalously synthesize the embryonic/simple epithelial keratin K8, and have lost the expression of the cell-cell adhesion receptor E-cadherin (E-CD). E-CD (+) cell clones (E62 and E24), obtained by transfection of an exogenous E-CD cDNA into HaCa4 cells, had a decreased ability to migrate through type IV collagen matrices. However, the E-CD (+) E62 clone remained as metastatic as the parental cell line, whereas the E24 clone, which does not take up the exogenous cDNA but spontaneously switches on the endogenous E-CD gene, suppressed the metastatic phenotype although it maintained its tumorigenicity. E24 cells had fivefold to sixfold lower levels of viral Ha-ras mRNA and p21 protein than the other cell lines. In addition, they did not synthesize K8 but rather switched on keratin K19. The comparison of E-CD proteins synthesized by E62 and E24 cell lines revealed no structural or functional differences because both localized at cell-cell contacts and associated with α-catenin, β-catenin, and plakoglobin. Furthermore, E-CD was still expressed in metastatic lung nodules produced by E62 cells. These results suggest that suppression of the metastatic phenotype in E24 cells occurs independently of E-CD expression and correlates with decreased levels of the oncogenic ras p21 protein.
URIhttp://hdl.handle.net/10261/79136
DOI10.1002/(SICI)1098-2744(199602)15:2<104::AID-MC3>3.0.CO;2-J
Identifiersdoi: 10.1002/(SICI)1098-2744(199602)15:2<104::AID-MC3>3.0.CO;2-J
issn: 0899-1987
e-issn: 1098-2744
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