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Oncogenic Transformation by the Signaling Adaptor Proteins Insulin Receptor Substrate (IRS)-1 and IRS-2

Open access
Dearth, Robert K., Cui, Xiaojiang, Kim, Hyun-Jung, Hadsell, Darryl L., Lee, Adrian V.·2007·Cell Cycle

Abstract

Insulin receptor substrates (IRSs) are adaptor proteins that link signaling from upstream activators to multiple downstream effectors to modulate normal growth, metabolism, survival, and differentiation. Recent cell culture studies have shown that IRSs can interact with, and are functionally required for, the transforming ability of many oncogenes. Consistent with this, IRSs are elevated and hyperactive in many human tumors. IRSs respond to many extracellular signals that are critical for mammary gland development, and we have shown that IRSs disrupt normal mammary acini formation in vitro, and cause mammary tumorigenesis and metastasis in vivo. In this review we will discuss the role of IRSs in both transformation and cancer progression.

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Metadata

Authors
Dearth, R. K., Cui, X., Kim, H.-J., Hadsell, D. L., & Lee, A. V.
Venue
Cell Cycle
Published
2007-03-15
Volume
6
Issue
6
Pages
705-713
ISSN
  • 1538-4101 (ISSN-L)
  • 1551-4005
OpenAlex
W2010223438
Cited by
167
References
0
FWCI
5.03
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Oncogenic Transformation by the Signaling Adaptor Proteins Insulin Receptor Substrate (IRS)-1 and IRS-2. https://app.cochat.ai/papers/10.4161/cc.6.6.4035
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Dearth, R. K., Cui, X., Kim, H.-J., Hadsell, D. L., & Lee, A. V. (2007). Oncogenic Transformation by the Signaling Adaptor Proteins Insulin Receptor Substrate (IRS)-1 and IRS-2. Cell Cycle. https://doi.org/10.4161/cc.6.6.4035

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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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