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Cited by 295

The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.

STAT‐mediated EGFR signaling in cancer

Quesnelle, Kelly M., Boehm, Amanda L., Grandis, Jennifer R.·2007·Journal of Cellular Biochemistry

Abstract

The epidermal growth factor receptor (EGFR) and signal transducers and activators of transcription (STATs) are commonly expressed and activated in many malignancies. EGFR is an upstream activator of several pathways involved in tumor progression, and STATs activate selected genes involved in oncogenesis. There are several different mechanisms by which STAT proteins can mediate intracellular EGFR signaling, including direct activation of STATs by EGFR binding and indirect activation of STATs through Src‐mediated EGFR signaling. EGFR likely activates STAT in a manner distinctive from other mechanisms of STAT activation; STAT5 can be phosphorylated in an EGF‐dependent manner at unique sites, conferring novel functions. Cumulative evidence suggests that targeting EGFR signaling pathways at several levels may demonstrate synergistic therapeutic effects compared with targeting the upstream receptor alone. Thus, methods to inhibit EGFR in conjunction with oncogenic STATs may represent a novel therapeutic strategy for cancers characterized by upregulation of EGFR signaling. J. Cell. Biochem. 102: 311–319, 2007. © 2007 Wiley‐Liss, Inc.

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Metadata

Authors
Quesnelle, K. M., Boehm, A. L., & Grandis, J. R.
Venue
Journal of Cellular Biochemistry
Publisher
Wiley
Published
2007-07-27
Volume
102
Issue
2
Pages
311-319
ISSN
  • 0730-2312 (ISSN-L)
  • 1097-4644
OpenAlex
W2073723168
Cited by
295
References
46
FWCI
6.04
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: STAT‐mediated EGFR signaling in cancer. https://app.cochat.ai/papers/10.1002/jcb.21475
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Quesnelle, K. M., Boehm, A. L., & Grandis, J. R. (2007). STAT‐mediated EGFR signaling in cancer. Journal of Cellular Biochemistry. https://doi.org/10.1002/jcb.21475

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

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