The type I insulin-like growth factor receptor pathway: a key player in cancer therapeutic resistance
被引:105
作者:
Casa, Angelo J.
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Baylor Coll Med, Dept Med, Breast Ctr, Houston, TX 77030 USA
Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USASt Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USA
Casa, Angelo J.
[2
,3
]
Dearth, Robert K.
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机构:
Baylor Coll Med, Dept Med, Breast Ctr, Houston, TX 77030 USA
Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USASt Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USA
Dearth, Robert K.
[2
,3
]
Litzenburger, Beate C.
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机构:
Baylor Coll Med, Dept Med, Breast Ctr, Houston, TX 77030 USA
Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USASt Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USA
Litzenburger, Beate C.
[2
,3
]
Lee, Adrian V.
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机构:
Baylor Coll Med, Dept Med, Breast Ctr, Houston, TX 77030 USA
Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USASt Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USA
Lee, Adrian V.
[2
,3
]
Cui, Xiaojiang
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St Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USASt Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USA
Cui, Xiaojiang
[1
]
机构:
[1] St Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USA
[2] Baylor Coll Med, Dept Med, Breast Ctr, Houston, TX 77030 USA
The insulin-like growth factor (IGF) ligands stimulate cellular proliferation and survival by activating the type I insulin-like growth factor receptor (IGF-IR). As a result, the IGF signaling system is implicated in a number of cancers, including those of the breast, prostate, and lung. In addition to mitogenic and anti-apoptotic roles that may directly influence tumor development, IGF-IR also appears to be a critical determinant of response to numerous cancer therapies. This review describes the role of the IGF-IR pathway in mediating resistance to both general cytotoxic therapies, such as radiation and chemotherapy, and targeted therapies, such as tamoxifen and trastuzumab. It concludes with a description of approaches to target IGF-IR and argues that inhibition of IGF signaling, in conjunction with standard therapies, may enhance the response of cancer cells to multiple modalities.