Polo-like kinase 1 inhibitors and their potential role in anticancer therapy, with a focus on NSCLC

Clin Cancer Res. 2011 Oct 15;17(20):6459-66. doi: 10.1158/1078-0432.CCR-11-0541.

Abstract

Cytotoxic platinum-doublet chemotherapy that includes antimitotic agents is a current standard of care in advanced non-small cell lung cancer (NSCLC). Microtubule-targeting antimitotics, taxanes, and Vinca alkaloids are effective anticancer therapeutics that affect both dividing and nondividing cells. A new generation of antimitotic agents that target regulatory proteins-mitotic kinases and kinesins-has the potential to overcome the limitations related to the role of tubulin in nondividing cells that are associated with traditional antimitotics. This review concentrates on Polo-like kinase 1, a key regulator of mitosis, outlines a rationale for its development as an anticancer target, and discusses data from preclinical and clinical studies of Plk1 inhibitors with a particular focus on NSCLC.

Publication types

  • Review

MeSH terms

  • Antimitotic Agents / therapeutic use
  • Antineoplastic Agents / therapeutic use*
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Cell Cycle Proteins / antagonists & inhibitors*
  • Clinical Trials as Topic
  • Humans
  • Molecular Targeted Therapy
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Proto-Oncogene Proteins / antagonists & inhibitors*

Substances

  • Antimitotic Agents
  • Antineoplastic Agents
  • Cell Cycle Proteins
  • Proto-Oncogene Proteins
  • Protein Serine-Threonine Kinases