miR-6883 Family miRNAs Target CDK4/6 to Induce G1 Phase Cell-Cycle Arrest in Colon Cancer Cells

被引:53
作者
Lulla, Amriti R. [1 ,2 ]
Slifker, Michael J. [1 ]
Zhou, Yan [1 ]
Lev, Avital [1 ]
Einarson, Margret B. [1 ]
Dicker, David T. [1 ]
El-Deiry, Wafik S. [1 ,2 ]
机构
[1] Fox Chase Canc Ctr, 333 Cottman Ave,Room P2035, Philadelphia, PA 19111 USA
[2] Penn State Coll Med, Hershey, PA USA
关键词
X-LINKED INHIBITOR; FORKHEAD BOX M1; COLORECTAL-CANCER; FOXM1; EXPRESSION; TUMOR-SUPPRESSOR; CHEMOTHERAPY RESISTANCE; MESENCHYMAL TRANSITION; MICRORNA DYSREGULATION; APOPTOSIS PROTEIN; POOR-PROGNOSIS;
D O I
10.1158/0008-5472.CAN-17-1767
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CDK4/6 targeting is a promising therapeutic strategy under development for various tumor types. In this study, we used computational methods and The Cancer Genome Atlas dataset analysis to identify novel miRNAs that target CDK4/6 and exhibit potential for therapeutic development in colorectal cancer. The 3'UTR of CDK4/6 mRNAs are targeted by a family of miRNAs, which includes miR-6883-5p, miR-149(star), miR-6785-5p, and miR-4728-5p. Ectopic expression of miR-6883-5p or miR-149(star) downregulated CDK4 and CDK6 levels in human colorectal cancer cells. RNA-seq analysis revealed an inverse relationship between the expression of CDK4/6 and miR-149(star) and intronic miRNA-6883-5p encoding the clock gene PER1 in colorectal cancer patient samples. Restoring expression of miR-6883-5p and miR-149(star) blocked cell growth leading to G(0)-G(1) phase cell-cycle arrest and apoptosis in colorectal cancer cells. CDK4/6 targeting by miR-6883-5p and miR-149(star) could only partially explain the observed antiproliferative effects. Notably, both miRNAs synergized with the frontline colorectal cancer chemotherapy drug irinotecan. Further, they resensitized mutant p53-expressing cell lines resistant to 5-fluorouracil. Taken together, our results established the foundations of a candidate miRNA-based theranostic strategy to improve colorectal cancer management. (C) 2017 AACR.
引用
收藏
页码:6902 / 6913
页数:12
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