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      The Strange Case of CDK4/6 Inhibitors: Mechanisms, Resistance, and Combination Strategies

      research-article
      1 , 2 , 1 , 2 , 3
      Trends in cancer
      Cell Cycle, Cyclin D1, E2F, RB, Breast Cancer

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          Abstract

          CDK4/6 inhibitors have emerged as a powerful class of agents with clinical activity in a number of malignancies. Targeting the cell cycle represents a core attack on a defining feature of cancer. However, the mechanisms through which selective CDK4/6 targeted agents act has few parallels in the current pharmaceutical armamentarium against cancer. Notably, CDK4/6 inhibitors act downstream of most mitogenic signaling cascades, which have implications both related to clinical efficacy and resistance. Core knowledge of cell cycle processes has provided insights into mechanisms of intrinsic resistance to CDK4/6 inhibitors; however, the basis of acquired resistance versus durable response is only beginning to emerge. This review focuses on the mechanism of action and biomarkers to direct the precision use of CDK4/6 inhibitors and rationally-developed combination therapies.

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          Author and article information

          Journal
          101665956
          44235
          Trends Cancer
          Trends Cancer
          Trends in cancer
          2405-8033
          2405-8025
          7 December 2016
          January 2017
          01 January 2018
          : 3
          : 1
          : 39-55
          Affiliations
          [1 ]University of Arizona Cancer Center
          [2 ]Department of Medicine, University of Arizona
          [3 ]Department of Pathology, University of Arizona
          Author notes
          Correspondence: Erik S. Knudsen, University of Arizona Cancer Center, 1515 N Campbell Avenue, Suite 4963, University of Arizona, Tucson, AZ 85724, eknudsen@ 123456email.arizona.edu . Agnieszka Witkiewicz, University of Arizona Cancer Center, 1515 N Campbell Avenue, Suite 4963, University of Arizona, Tucson, AZ 85724, awitki@ 123456email.arizona.edu
          Article
          PMC5347397 PMC5347397 5347397 nihpa834450
          10.1016/j.trecan.2016.11.006
          5347397
          28303264
          2ab7e08a-ea67-4a4b-a182-112d39c91902
          History
          Categories
          Article

          Cyclin D1,RB,Breast Cancer,E2F,Cell Cycle
          Cyclin D1, RB, Breast Cancer, E2F, Cell Cycle

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