Molecular defects in mastocytosis: KIT and beyond KIT

Immunol Allergy Clin North Am. 2014 May;34(2):239-62. doi: 10.1016/j.iac.2014.01.009.

Abstract

In all variants of mastocytosis, activating KIT mutations are frequently found. In adults, neoplastic mast cells (MCs) cells show the KIT mutation D816V, whereas in children, MCs invading the skin are frequently positive for non-KIT D816V mutations. The clinical course and prognosis of the disease vary among patients with systemic mastocytosis (SM). Additional KIT-independent molecular defects might cause progression. Additional oncogenic lesions have recently been identified in advanced SM. In advanced SM the presence of additional genetic lesions or altered signaling worsening the prognosis might lead to the use of alternative therapies such as combined antisignaling targeted treatments or stem cell transplantation.

Keywords: ASXL1; KIT; Mutation; Signaling; Spliceosome; Systemic mastocytosis; TET2; Targeted therapy.

MeSH terms

  • Bone Marrow / drug effects
  • Bone Marrow / metabolism
  • Bone Marrow / pathology
  • Cell Proliferation
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Dioxygenases
  • Exons
  • Gene Expression Regulation, Neoplastic*
  • Hematologic Neoplasms / diagnosis
  • Hematologic Neoplasms / drug therapy
  • Hematologic Neoplasms / genetics*
  • Hematologic Neoplasms / pathology
  • Humans
  • Mast Cells / drug effects
  • Mast Cells / metabolism*
  • Mast Cells / pathology
  • Mastocytosis / diagnosis
  • Mastocytosis / drug therapy
  • Mastocytosis / genetics*
  • Mastocytosis / pathology
  • Mutation
  • Protein Kinase Inhibitors / therapeutic use
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-kit / genetics*
  • Proto-Oncogene Proteins c-kit / metabolism
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Signal Transduction
  • Spliceosomes / genetics*
  • Spliceosomes / metabolism
  • Spliceosomes / pathology
  • Stem Cell Factor / genetics
  • Stem Cell Factor / metabolism

Substances

  • ASXL1 protein, human
  • DNA-Binding Proteins
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins
  • Repressor Proteins
  • Stem Cell Factor
  • Dioxygenases
  • TET2 protein, human
  • Proto-Oncogene Proteins c-kit