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Molecular and Cellular Biology
Article . 1998 . Peer-reviewed
License: ASM Journals Non-Commercial TDM
Data sources: Crossref
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Identification of rCop-1, a New Member of the CCN Protein Family, as a Negative Regulator for Cell Transformation

Authors: R, Zhang; L, Averboukh; W, Zhu; H, Zhang; H, Jo; P J, Dempsey; R J, Coffey; +2 Authors

Identification of rCop-1, a New Member of the CCN Protein Family, as a Negative Regulator for Cell Transformation

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.

Keywords

Aging, Base Sequence, Genes, Viral, Carcinogenicity Tests, Cell Cycle, Molecular Sequence Data, Gene Expression, Apoptosis, Fibroblasts, Genes, p53, Cell Line, Rats, CCN Intercellular Signaling Proteins, Repressor Proteins, Mice, Cell Transformation, Neoplastic, Genes, ras, Retroviridae, Animals, Amino Acid Sequence

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    145
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
145
Top 10%
Top 1%
Top 1%
bronze