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Cited by 361

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Dependence of Cyclin E-CDK2 Kinase Activity on Cell Anchorage

Fang, Fang, Orend, Gertraud, Watanabe, Nobumoto, Hunter, Tony, Ruoslahti, Erkki·1996·Science

Abstract

Most nonmalignant cells are anchorage-dependent; they require substrate attachment for growth and, in some instances, survival. This requirement is lost on oncogenic transformation. The cyclin E-CDK2 complex, which is required for the G 1 -S transition of the cell cycle, was activated in late G 1 phase in attached human fibroblasts, but not in fibroblasts maintained in suspension. In transformed fibroblasts the complex was active regardless of attachment. The lack of cyclin E-CDK2 activity in suspended cells appeared to result from increased expression of CDK2 inhibitors and a concomitant decrease in phosphorylation of CDK2 on threonine-160. Suppression of cyclin E-CDK2 activity may thus underlie the anchorage dependence of cell growth.

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Crossref · 10.1126/science.271.5248.499

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Metadata

Authors
Fang, F., Orend, G., Watanabe, N., Hunter, T., & Ruoslahti, E.
Venue
Science
Published
1996-01-26
Volume
271
Issue
5248
Pages
499-502
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2035641694
Cited by
361
References
1
FWCI
23.83
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Dependence of Cyclin E-CDK2 Kinase Activity on Cell Anchorage. https://app.cochat.ai/papers/10.1126/science.271.5248.499
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Fang, F., Orend, G., Watanabe, N., Hunter, T., & Ruoslahti, E. (1996). Dependence of Cyclin E-CDK2 Kinase Activity on Cell Anchorage. Science. https://doi.org/10.1126/science.271.5248.499

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.