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Cited by 488

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Normal and cancer-related functions of the p160 steroid receptor co-activator (SRC) family

Open access
Xu, Jianming, Wu, Ray-Chang, O'Malley, Bert W.·2009·Nature Reviews Cancer

Abstract

The three homologous members of the p160 SRC family (SRC1, SRC2 and SRC3) mediate the transcriptional functions of nuclear receptors and other transcription factors, and are the most studied of all the transcriptional co-activators. Recent work has indicated that the SRCgenes are subject to amplification and overexpression in various human cancers. Some of the molecular mechanisms responsible for SRC overexpression, along with the mechanisms by which SRCs promote breast and prostate cancer cell proliferation and survival, have been identified, as have the specific contributions of individual SRC family members to spontaneous breast and prostate carcinogenesis in genetically manipulated mouse models. These studies have identified new challenges for cancer research and therapy.

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Metadata

Authors
Xu, J., Wu, R.-C., & O'Malley, B. W.
Venue
Nature Reviews Cancer
Published
2009-09
Volume
9
Issue
9
Pages
615-630
ISSN
  • 1474-175X (ISSN-L)
  • 1474-1768
OpenAlex
W1977027014
Cited by
488
References
5
FWCI
2.62
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Normal and cancer-related functions of the p160 steroid receptor co-activator (SRC) family. https://app.cochat.ai/papers/10.1038/nrc2695
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Xu, J., Wu, R.-C., & O'Malley, B. W. (2009). Normal and cancer-related functions of the p160 steroid receptor co-activator (SRC) family. Nature Reviews Cancer. https://doi.org/10.1038/nrc2695

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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.