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Identification of rCop-1, a new member of the CCN protein family, as a negative regulator for cell transformation.
Zhang, R; Averboukh, L; Zhu, W; Zhang, H; Jo, H; Dempsey, P J; Coffey, R J; Pardee, A B; Liang, P.
Affiliation
  • Zhang R; Vanderbilt Cancer Center, Department of Cell Biology, Vanderbilt University, Nashville, Tennessee 37232, USA.
Mol Cell Biol ; 18(10): 6131-41, 1998 Oct.
Article in En | MEDLINE | ID: mdl-9742130
ABSTRACT
By using a model system for cell transformation mediated by the cooperation of the activated H-ras oncogene and the inactivated p53 tumor suppressor gene, rCop-1 was identified by mRNA differential display as a gene whose expression became lost after cell transformation. Homology analysis indicates that rCop-1 belongs to an emerging cysteine-rich growth regulator family called CCN, which includes connective-tissue growth factor, CYR61, CEF10 (v-src inducible), and the product of the nov proto-oncogene. Unlike the other members of the CCN gene family, rCop-1 is not an immediate-early gene, it lacks the conserved C-terminal domain which was shown to confer both growth-stimulating and heparin-binding activities, and its expression is lost in cells transformed by a variety of mechanisms. Ectopic expression of rCop-1 by retroviral gene transfers led to cell death in a transformation-specific manner. These results suggest that rCop-1 represents a new class of CCN family proteins that have functions opposing those of the previously identified members.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / Cell Transformation, Neoplastic / Genes, p53 / Genes, ras Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals Language: En Journal: Mol Cell Biol Year: 1998 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / Cell Transformation, Neoplastic / Genes, p53 / Genes, ras Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals Language: En Journal: Mol Cell Biol Year: 1998 Document type: Article Affiliation country:
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