1. Academic Validation
  2. Discovery of a selective inhibitor of doublecortin like kinase 1

Discovery of a selective inhibitor of doublecortin like kinase 1

  • Nat Chem Biol. 2020 Jun;16(6):635-643. doi: 10.1038/s41589-020-0506-0.
Fleur M Ferguson  # 1 2 Behnam Nabet  # 1 2 Srivatsan Raghavan 3 4 Yan Liu 5 Alan L Leggett 1 Miljan Kuljanin 6 Radha L Kalekar 3 4 Annan Yang 3 4 Shuning He 7 Jinhua Wang 1 2 Raymond W S Ng 3 4 Rita Sulahian 4 Lianbo Li 5 Emily J Poulin 8 Ling Huang 8 Jost Koren 9 Nora Dieguez-Martinez 10 Sergio Espinosa 10 Zhiyang Zeng 11 Cesear R Corona 11 James D Vasta 11 Ryoma Ohi 12 Taebo Sim 13 Nam Doo Kim 14 Wayne Harshbarger 4 15 Jose M Lizcano 10 Matthew B Robers 11 Senthil Muthaswamy 8 16 Charles Y Lin 9 A Thomas Look 7 17 Kevin M Haigis 8 18 Joseph D Mancias 6 Brian M Wolpin 3 19 Andrew J Aguirre 3 4 19 William C Hahn 3 4 19 Kenneth D Westover 5 Nathanael S Gray 20 21
Affiliations

Affiliations

  • 1 Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • 2 Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.
  • 3 Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • 4 Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • 5 Departments of Biochemistry and Radiation Oncology, the University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • 6 Division of Radiation and Genome Stability, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • 7 Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • 8 Cancer Research Institute and Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
  • 9 Department of Molecular and Human Genetics, Therapeutic Innovation Center Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX, USA.
  • 10 Departament de Bioquímica i Biologia Molecular & Institut de Neurociencies, Facultat de Medicina. Universitat Autonoma de Barcelona, Bellaterra, Spain.
  • 11 Promega Corporation, Madison, WI, USA.
  • 12 Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
  • 13 Chemical Kinomics Research Center, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea and KU-KIST Graduate School of Converging Science and Technology, Korea University, Seoul, Republic of Korea.
  • 14 NDBio Therapeutics Inc, Incheon, Republic of Korea.
  • 15 GSK Vaccines, Rockville, MD, USA.
  • 16 Departments of Medicine and Pathology, Harvard Medical School, Boston, MA, USA.
  • 17 Division of Pediatric Hematology/Oncology, Boston Children's Hospital, Boston, MA, USA.
  • 18 Harvard Digestive Disease Center, Harvard Medical School, Boston, MA, USA.
  • 19 Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
  • 20 Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, USA. [email protected].
  • 21 Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA. [email protected].
  • # Contributed equally.
Abstract

Doublecortin Like Kinase 1 (DCLK1) is an understudied kinase that is upregulated in a wide range of cancers, including pancreatic ductal adenocarcinoma (PDAC). However, little is known about its potential as a therapeutic target. We used chemoproteomic profiling and structure-based design to develop a selective, in vivo-compatible chemical probe of the DCLK1 kinase domain, DCLK1-IN-1. We demonstrate activity of DCLK1-IN-1 against clinically relevant patient-derived PDAC organoid models and use a combination of RNA-sequencing, proteomics and phosphoproteomics analysis to reveal that DCLK1 inhibition modulates proteins and pathways associated with cell motility in this context. DCLK1-IN-1 will serve as a versatile tool to investigate DCLK1 biology and establish its role in Cancer.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-135985
    99.62%, DCLK1/2 Inhibitor