4.6 Article

Overcoming resistance to tyrosine kinase inhibitors Lessons learned from cancer cells treated with EGFR antagonists

期刊

CELL CYCLE
卷 8, 期 1, 页码 18-22

出版社

TAYLOR & FRANCIS INC
DOI: 10.4161/cc.8.1.7324

关键词

breast cancer; HER2; EGFR; tyrosine kinase inhibitors; TKI resistance; PI3K

资金

  1. NCI [R01 CA62212, R01 CA80195, T32 CA119910]
  2. ACS Clinical Research Professorship [CRP-07-234]
  3. Entertainment Industry Foundation
  4. Breast Cancer Specialized Program of Research Excellence (SPORE [P50 CA98131]
  5. Vanderbilt-Ingram Comprehensive Cancer Center [P30 CA68485]
  6. NIH K08 [CA120060-01]
  7. American Association for Cancer Research
  8. DF/HCC Lung Cancer Specialized Program SPORE [P50 CA090578]
  9. DF/HCC Gastrointestinal Cancer SPORE [P50 CA127003]
  10. NATIONAL CANCER INSTITUTE [T32CA119910, R01CA062212, P50CA090578, K08CA120060, P50CA098131, R01CA080195, P30CA068485, P50CA127003] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Tyrosine kinase inhibitors (TKIs) are effective anti-cancer therapies but resistance to these agents eventually develops. Several models of resistance to TKIs have been studied including resistance to EGFR inhibitors. Recent studies in EGFR-dependent A431 cells found upregulation of the IGF1R pathway as a mechanism to overcome blockade of EGFR. This was associated with amplification of IGF1R signaling and recovery of downstream PI3K-AKT activation. This work adds to a growing body of cell lines in culture that have provided insights into mechanisms of resistance that can be interrogated in primary tumors in patients. In this review, these model systems and their applicability to human cancers, as well as strategies to identify and overcome resistance to TKIs, are discussed.

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