Approaching the challenges of MKK3/p38delta MAPK targeting for therapeutic purpose in colorectal cancer

J Exp Clin Cancer Res. 2019 Dec 27;38(1):504. doi: 10.1186/s13046-019-1513-4.

Abstract

MKK3 is a member of the dual specificity kinase group specific upstream activator of p38 MAPK proteins. We originally identified MKK3 as mutant p53 (mutp53) gain-of-function (GOF) upregulated target gene in different tumor models. To deeply investigate the MKK3 functions in cancer, taking advantage of a panel of authenticated colorectal cancer (CRC) lines and primary colonocytes, we found that MKK3 activates specifically p38delta MAPK protein, which signaling is further triggered by 5-fluorouracil (5-FU) treatments, a largely adopted chemotherapeutic drug in CRC clinical practice. The overall achieved results proposed the MKK3/p38delta MAPK as relevant molecular axis involved in abrogating efficacy to 5-FU treatments in CRC. This commentary will provide an overall discussion of the results that have been achieved contextualizing them in the overview of the knowledge in the p38 MAPK field in cancer disease.

Keywords: Chemotherapy; Colorectal Cancer; Combined treatments; MKK3 / p38 MAPK signalling; Target therapy; p38 delta MAPK.

Publication types

  • Letter

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / pathology
  • Humans
  • MAP Kinase Kinase 3 / metabolism*
  • Mitogen-Activated Protein Kinase 13 / metabolism*
  • Molecular Targeted Therapy
  • Protein Kinase Inhibitors / pharmacology*
  • Protein Kinase Inhibitors / therapeutic use
  • Signal Transduction / drug effects*
  • Treatment Outcome

Substances

  • Protein Kinase Inhibitors
  • Mitogen-Activated Protein Kinase 13
  • MAP Kinase Kinase 3
  • MAP2K3 protein, human