Resistance to CDK4/6 Inhibitors in Estrogen Receptor-Positive Breast Cancer

被引:45
作者
Scheidemann, Erin R. [1 ]
Shajahan-Haq, Ayesha N. [1 ]
机构
[1] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Dept Oncol, Washington, DC 20057 USA
关键词
ER plus breast cancer; antiestrogens; CDK4; CDK4/6; inhibitor; palbociclib; ribociclib; abemaciclib; KINASE; 4/6; INHIBITOR; CELL-CYCLE CONTROL; ENDOCRINE THERAPY; PHASE-I; PLUS FULVESTRANT; OPEN-LABEL; PD; 0332991; PALBOCICLIB; ABEMACICLIB; COMBINATION;
D O I
10.3390/ijms222212292
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
Estrogen receptor-positive (ER+) breast cancer is the most common form of breast cancer. Antiestrogens were the first therapy aimed at treating this subtype, but resistance to these warranted the development of a new treatment option. CDK4/6 inhibitors address this problem by halting cell cycle progression in ER+ cells, and have proven to be successful in the clinic. Unfortunately, both intrinsic and acquired resistance to CDK4/6 inhibitors are common. Numerous mechanisms of how resistance occurs have been identified to date, including the activation of prominent growth signaling pathways, the loss of tumor-suppressive genes, and noncanonical cell cycle function. Many of these have been successfully targeted and demonstrate the ability to overcome resistance to CDK4/6 inhibitors in preclinical and clinical trials. Future studies should focus on the development of biomarkers so that patients likely to be resistant to CDK4/6 inhibition can initially be given alternative methods of treatment.
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页数:28
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