Adipocytes Promote Cisplatin Resistance through Secreting A1BG and Regulating NAMPT/PARP1 Axis-Mediated DNA Repair in Osteosarcoma

Adv Sci (Weinh). 2025 Sep;12(35):e02926. doi: 10.1002/advs.202502926. Epub 2025 Jun 25.

Abstract

Obesity is increasingly recognized as a negative prognostic factor for cancers, including osteosarcoma. However, the mechanisms linking obesity to chemoresistance in osteosarcoma remain unclear. This study found obesity is significantly associated with poor responses to cisplatin-based chemotherapy in osteosarcoma patients. In vitro, adipocyte-conditioned medium (Adi-CM) induced cisplatin resistance, while peritumoral adipocytes and diet-induced obesity (DIO) reduce the cisplatin efficacy in vivo. Mechanistically, Adi-CM enhanced DNA repair by the PARP1/ATM pathway activation. Proteomic analysis identified A1BG, a secreted protein upregulated in adipocytes from chemoresistant patients, as a key mediator of this effect. A1BG depletion in adipocytes restored cisplatin sensitivity, whereas recombinant A1BG enhanced resistance and promoted DNA repair. Further investigation revealed a direct interaction between A1BG and NAMPT, leading to the stabilization of NAMPT and an increased NAD+ production. This enhanced PARP1 activity and subsequent DNA repair. Importantly, pharmacological inhibition of NAMPT and PARP1 using FK886 and Olaparib, respectively, reversed Adi-CM-induced cisplatin resistance and restored cisplatin sensitivity in osteosarcoma cells, DIO mouse models, and patient-derived organoids. A novel link between obesity and cisplatin resistance in osteosarcoma is established, highlighting the A1BG/NAMPT/PARP1 axis as a critical driver. Targeting this axis may represent a promising therapeutic strategy for overcoming obesity-associated chemoresistance in osteosarcoma.

Keywords: adipocytes; cisplatin resistance; dna repair; osteosarcoma.

MeSH terms

  • Adipocytes* / metabolism
  • Animals
  • Antineoplastic Agents / pharmacology
  • Bone Neoplasms* / drug therapy
  • Bone Neoplasms* / genetics
  • Bone Neoplasms* / metabolism
  • Cell Line, Tumor
  • Cisplatin* / pharmacology
  • Cisplatin* / therapeutic use
  • Cytokines* / genetics
  • Cytokines* / metabolism
  • DNA Repair* / drug effects
  • Drug Resistance, Neoplasm* / genetics
  • Humans
  • Male
  • Mice
  • Nicotinamide Phosphoribosyltransferase* / genetics
  • Nicotinamide Phosphoribosyltransferase* / metabolism
  • Obesity / metabolism
  • Osteosarcoma* / drug therapy
  • Osteosarcoma* / genetics
  • Osteosarcoma* / metabolism
  • Poly (ADP-Ribose) Polymerase-1* / genetics
  • Poly (ADP-Ribose) Polymerase-1* / metabolism

Substances

  • Cisplatin
  • Nicotinamide Phosphoribosyltransferase
  • Poly (ADP-Ribose) Polymerase-1
  • Cytokines
  • nicotinamide phosphoribosyltransferase, human
  • PARP1 protein, human
  • Antineoplastic Agents