The mechanism of UNC-51-like kinase 1 and the applications of small molecule modulators in cancer treatment

Eur J Med Chem. 2024 Mar 15:268:116273. doi: 10.1016/j.ejmech.2024.116273. Epub 2024 Feb 27.

Abstract

Autophagy is a process of self-renewal in cells, which not only provides the necessary nutrients for cells, but also clears necrotic organelles. Autophagy disorders are closely related to diseases such as cancer. UNC-51-like kinase 1 (ULK1) is a serine/threonine protein kinase that plays a crucial role in receiving input from energy and nutrient sensors, activating autophagy to maintain cellular homeostasis under stressful conditions. In recent years, targeting ULK1 has become a highly promising strategy for cancer treatment. This review introduces the regulatory mechanism of ULK1 in autophagy through the AMPK/mTOR/ULK1 pathway and reviews the research progress of ULK1 activators and inhibitors and their applications in cancer treatment. In addition, we analyze the binding modes between ULK1 and modulators through virtual molecular docking, which will provide a reliable basis and theoretical guidance for the design and development of new therapeutic drugs targeting ULK1.

Keywords: Autophagy; Cancer; Inhibitors; UNC-51-like kinase1.

Publication types

  • Review

MeSH terms

  • AMP-Activated Protein Kinases* / metabolism
  • Autophagy
  • Autophagy-Related Protein-1 Homolog / metabolism
  • Molecular Docking Simulation
  • Neoplasms* / drug therapy
  • Protein Serine-Threonine Kinases / metabolism

Substances

  • Autophagy-Related Protein-1 Homolog
  • AMP-Activated Protein Kinases
  • Protein Serine-Threonine Kinases