FOXM1 mediates methotrexate resistance in osteosarcoma cells by promoting autophagy

Acta Biochim Biophys Sin (Shanghai). 2024 Jul 31;56(9):1289-1299. doi: 10.3724/abbs.2024084.

Abstract

Osteosarcoma (OS) is a primary bone cancer mostly found in adolescents and elderly individuals. The treatment of OS is still largely dependent on traditional chemotherapy. However, the high incidence of drug resistance remains one of the greatest impediments to limiting improvements in OS treatment. Recent findings have indicated that the transcription factor FOXM1 plays an important role in various cancer-related events, especially drug resistance. However, the possible role of FOXM1 in the resistance of OS to methotrexate (MTX) remains to be explored. Here, we find that FOXM1, which confers resistance to MTX, is highly expressed in OS tissues and MTX-resistant cells. FOXM1 overexpression promotes MTX resistance by enhancing autophagy in an HMMR/ATG7-dependent manner. Importantly, silencing of FOXM1 or inhibiting autophagy reverses drug resistance. These findings demonstrate a new mechanism for FOXM1-induced MTX resistance and provide a promising target for improving OS chemotherapy outcomes.

Keywords: FOXM1; drug resistance; methotrexate; osteosarcoma.

MeSH terms

  • Antimetabolites, Antineoplastic / pharmacology
  • Autophagy* / drug effects
  • Autophagy* / genetics
  • Bone Neoplasms* / drug therapy
  • Bone Neoplasms* / genetics
  • Bone Neoplasms* / metabolism
  • Bone Neoplasms* / pathology
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm* / genetics
  • Forkhead Box Protein M1* / genetics
  • Forkhead Box Protein M1* / metabolism
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Methotrexate* / pharmacology
  • Osteosarcoma* / drug therapy
  • Osteosarcoma* / genetics
  • Osteosarcoma* / metabolism
  • Osteosarcoma* / pathology

Substances

  • Methotrexate
  • Forkhead Box Protein M1
  • FOXM1 protein, human
  • Antimetabolites, Antineoplastic

Grants and funding

This work was supported by the grant from the Natural Science Foundation of Qingdao, Shandong (No. 22-3-7-smjk-7-nsh).