Novel therapeutic approaches in chondrosarcoma

Future Oncol. 2017 Mar;13(7):637-648. doi: 10.2217/fon-2016-0226. Epub 2017 Jan 30.

Abstract

Chondrosarcoma is a malignant tumor of bones, characterized by the production of cartilage matrix. Due to lack of effective treatment for advanced disease, the clinical management of chondrosarcomas is exceptionally challenging. Current research focuses on elucidating the molecular events underlying the pathogenesis of this rare bone malignancy, with the goal of developing new molecularly targeted therapies. Signaling pathways suggested to have a role in chondrosarcoma include Hedgehog, Src, PI3k-Akt-mTOR and angiogenesis. Mutations in IDH1/2, present in more than 50% of primary conventional chondrosarcomas, make the development of IDH inhibitors a promising treatment option. The present review discusses the preclinical and early clinical data on novel targeted therapeutic approaches in chondrosarcoma.

Keywords: HDACIs; Hedgehog pathway; IDH1/2; Src pathway; chondrosarcoma; novel agents; treatment.

Publication types

  • Review

MeSH terms

  • Angiogenesis Inhibitors / pharmacology
  • Angiogenesis Inhibitors / therapeutic use
  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Chondrosarcoma / drug therapy*
  • Chondrosarcoma / genetics
  • Chondrosarcoma / metabolism
  • Disease Management
  • Hedgehog Proteins / metabolism
  • Histone Deacetylase Inhibitors / pharmacology
  • Histone Deacetylase Inhibitors / therapeutic use
  • Humans
  • Isocitrate Dehydrogenase / genetics
  • Isocitrate Dehydrogenase / metabolism
  • Molecular Targeted Therapy*
  • Mutation
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / drug effects
  • TOR Serine-Threonine Kinases / metabolism
  • src-Family Kinases / metabolism

Substances

  • Angiogenesis Inhibitors
  • Antineoplastic Agents
  • Hedgehog Proteins
  • Histone Deacetylase Inhibitors
  • Protein Kinase Inhibitors
  • Isocitrate Dehydrogenase
  • src-Family Kinases
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases