CDK-Independent Activation of Estrogen Receptor by Cyclin D1
Cell, ISSN: 0092-8674, Vol: 88, Issue: 3, Page: 405-415
1997
- 638Citations
- 159Captures
- 7Mentions
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations638
- Citation Indexes638
- 638
- CrossRef461
- Captures159
- Readers159
- 159
- Mentions7
- References7
- Wikipedia7
Article Description
Both cyclin D1 and estrogens have an essential role in regulating proliferation of breast epithelial cells. We show here a novel role for cyclin D1 in growth regulation of estrogen-responsive tissues by potentiating transcription of estrogen receptor–regulated genes. Cyclin D1 mediates this activation independent of complex formation to a CDK partner. Cyclin D1 activates estrogen receptor–mediated transcription in the absence of estrogen and enhances transcription in its presence. The activation of estrogen receptor by cyclin D1 is not inhibited by anti-estrogens. A direct physical binding of cyclin D1 to the hormone binding domain of the estrogen receptor results in an increased binding of the receptor to estrogen response element sequences, and upregulates estrogen receptor–mediated transcription. These results highlight a novel role for cyclin D1 as a CDK-independent activator of the estrogen receptor.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0092867400818796; http://dx.doi.org/10.1016/s0092-8674(00)81879-6; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0030968438&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/9039267; http://linkinghub.elsevier.com/retrieve/pii/S0092867400818796; http://api.elsevier.com/content/article/PII:S0092867400818796?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0092867400818796?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/S0092867400818796; http://dx.doi.org/10.1016/s0092-8674%2800%2981879-6; https://dx.doi.org/10.1016/s0092-8674%2800%2981879-6; http://www.cell.com/cell/abstract/S0092-8674(00)81879-6?_returnURL=http%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0092867400818796%3Fshowall%3Dtrue; http://www.cell.com/article/S0092867400818796/abstract; http://www.cell.com/article/S0092867400818796/fulltext; http://www.cell.com/article/S0092867400818796/pdf
Elsevier BV
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