CDK4 regulates cancer stemness and is a novel therapeutic target for triple-negative breast cancer

被引:47
作者
Dai, Meiou [1 ]
Zhang, Chenjing [1 ]
Ali, Ayad [1 ]
Hong, Xinyuan [1 ]
Tian, Jun [1 ]
Lo, Chieh [1 ]
Fils-Aime, Nadege [1 ]
Burgos, Sergio A. [2 ]
Ali, Suhad [1 ]
Lebrun, Jean-Jacques [1 ]
机构
[1] McGill Univ, Dept Med, Ctr Hlth, Canc Res Program, Montreal, PQ H4A 3J1, Canada
[2] McGill Univ, Dept Anim Sci, Ste Anne De Bellevue, PQ H9X 3V9, Canada
关键词
CELL-MIGRATION; MAMMARY STEM; DIFFERENTIATION; OVEREXPRESSION; IDENTIFICATION; HETEROGENEITY; PREDICTOR; EXPANSION; MARKER; G1;
D O I
10.1038/srep35383
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Triple negative breast cancers exhibit very aggressive features and poor patient outcomes. These tumors are enriched in cancer stem cells and exhibit resistance to most treatments and chemotherapy. In this study, we found the cyclin-dependent kinase (CDK4) to act as a cancer stem cell regulator and novel prognostic marker in triple negative breast cancers. We found CDK4 to be highly expressed in these tumors and its expression to correlate with poor overall and relapse free survival outcomes, high tumor grade and poor prognostic features of triple negative breast cancer patients. Moreover, we found that blocking CDK4 expression or kinase activity, using a pharmacological inhibitor prevented breast cancer stem cell self-renewal. Interestingly, suppression of CDK4 expression or kinase activity reversed the basal-B TNBC mesenchymal phenotype to an epithelial-and luminal-like phenotype which correlates with better clinical prognosis. Finally, blocking CDK4 activity efficiently eliminated both normal and chemotherapy-resistant cancer cells in triple negative breast cancers, highlighting CDK4 as a promising novel therapeutic target for these aggressive breast tumors.
引用
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页数:15
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