Principles of Resistance to Targeted Cancer Therapy: Lessons from Basic and Translational Cancer Biology

被引:117
|
作者
Sabnis, Amit J. [1 ,2 ,3 ]
Bivona, Trever G. [2 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
关键词
CELL LUNG-CANCER; TO-MESENCHYMAL TRANSITION; PROSTATE-CANCER; ANDROGEN-RECEPTOR; TUMOR HETEROGENEITY; ACQUIRED-RESISTANCE; TYROSINE KINASE; MOLECULAR DETERMINANTS; CUTANEOUS MELANOMA; IMPROVED SURVIVAL;
D O I
10.1016/j.molmed.2018.12.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Identification of the genomic drivers of cancer has led to the clinical development of targeted therapies that strike at the heart of many malignancies. Nonetheless, many cancers outsmart such precision-medicine efforts, and thus therapeutic resistance contributes significantly to cancer mortality. Attempts to understand the basis for resistance in patient samples and laboratory models has yielded two major benefits: one, more effective chemical inhibitors and rational combination therapies are now employed to prevent or circumvent resistance pathways; and two, our understanding of how oncogenic mutations drive cancer cell survival and oncogene addiction is deeper and broader, highlighting downstream or parallel cellular programs that shape these phenotypes. This review discusses emerging principles of resistance to therapies targeted against key oncogenic drivers.
引用
收藏
页码:185 / 197
页数:13
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