Hyperthermia generated by magnetic nanoparticles for effective treatment of disseminated peritoneal cancer in an orthotopic nude-mouse model

Cell Cycle. 2021 Jun;20(12):1122-1133. doi: 10.1080/15384101.2021.1919441. Epub 2021 Jun 10.

Abstract

Magnetic hyperthermia (MHT), which combines magnetic nanoparticles (MNPs) with an alternating magnetic field (AMF), holds promise as a cancer therapy. There have been many studies about hyperthermia, most of which have been performed by direct injection of MNPs into tumor tissues. However, there have been no reports of treating peritoneal disseminated disease with MHT to date. In the present study, we treated peritoneal metastasis of gastric cancer with MHT using superparamagnetic iron oxide (Fe3O4) nanoparticle (SPION) coated with carboxydextran as an MNP, in an orthotopic mouse model mimicking early peritoneal disseminated disease of gastric cancer. SPIONs of an optimal size were intraperitoneally administered, and an AMF (390 kHz, 28 kAm-1) was applied for 10 minutes, four times every three days. Three weeks after the first MHT treatment, the peritoneal metastases were significantly inhibited compared with the AMF-alone group or the untreated-control group. The results of the present study show that MHT can be applied as a new treatment option for disseminated peritoneal gastric cancer.Abbreviations: AMF: alternating magnetic field; Cy1: cytology-positive; DMEM: Dulbecco's Modified Eagle's Medium; FBS: fetal bovine serum; H&E: hematoxylin and eosin; HIPEC: hyperthermic intraperitoneal chemotherapy; MEM: Minimum Essential Medium; MHT: magnetic hyperthermia; MNPs: magnetic nanoparticles; P0: macroscopic peritoneal dissemination; RFP: red fluorescent protein; SPION: superparamagnetic iron oxide (Fe3O4) nanoparticle.

Keywords: Hyperthermia; disseminated cancer; gastric cancer; magnetic nanoparticles; milky spot; nude mice; orthotopic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival
  • Disease Models, Animal
  • HCT116 Cells
  • Humans
  • Hyperthermia, Induced / methods*
  • Iron / administration & dosage*
  • Luminescent Proteins / metabolism
  • Magnetic Fields*
  • Magnetite Nanoparticles / administration & dosage*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Optical Imaging / methods
  • Oxides / administration & dosage*
  • Peritoneal Neoplasms / secondary*
  • Peritoneal Neoplasms / therapy*
  • Red Fluorescent Protein
  • Stomach Neoplasms / pathology*
  • Treatment Outcome

Substances

  • Luminescent Proteins
  • Magnetite Nanoparticles
  • Oxides
  • carboxydextran-coated magnetic iron oxide particles
  • Iron

Grants and funding

This work was supported by the JSPS KAKENHI [JP19K07730]; JSPS KAKENHI [JP15K09959].