The role of aurora A and polo-like kinases in high-risk lymphomas

Blood Adv. 2019 Jun 11;3(11):1778-1787. doi: 10.1182/bloodadvances.2019000232.

Abstract

High-risk lymphomas (HRLs) are associated with dismal outcomes and remain a therapeutic challenge. Recurrent genetic and molecular alterations, including c-myc expression and aurora A kinase (AAK) and polo-like kinase-1 (PLK1) activation, promote cell proliferation and contribute to the highly aggressive natural history associated with these lymphoproliferative disorders. In addition to its canonical targets regulating mitosis, the AAK/PLK1 axis directly regulates noncanonical targets, including c-myc. Recent studies demonstrate that HRLs, including T-cell lymphomas and many highly aggressive B-cell lymphomas, are dependent upon the AAK/PLK1 axis. Therefore, the AAK/PLK1 axis has emerged as an attractive therapeutic target in these lymphomas. In addition to reviewing these recent findings, we summarize the rationale for targeting AAK/PLK1 in high-risk and c-myc-driven lymphoproliferative disorders.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Aurora Kinase A / metabolism*
  • Cell Cycle Proteins / metabolism*
  • Humans
  • Lymphoma, B-Cell / enzymology*
  • Lymphoma, B-Cell / pathology
  • Lymphoma, B-Cell / therapy
  • Lymphoma, T-Cell / enzymology*
  • Lymphoma, T-Cell / pathology
  • Lymphoma, T-Cell / therapy
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-myc / metabolism
  • Risk Factors
  • Signal Transduction*

Substances

  • Cell Cycle Proteins
  • MYC protein, human
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-myc
  • AURKA protein, human
  • Aurora Kinase A
  • Protein Serine-Threonine Kinases