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Hyperthermia generated with ferucarbotran (Resovist®) in an alternating magnetic field enhances cisplatin-induced apoptosis of cultured human oral cancer cells

Authors :
Kayoko Oda
Utako Yokoyama
Akiyoshi Miyajima
Motohiko Sato
Haruki Eguchi
Itaru Sato
Toshinori Iwai
Xianfeng Feng
Takayuki Fujita
Satoshi Okumura
Hideyuki Nakashima
Yoshihiro Ishikawa
Ayako Makino
Mitomu Kioi
Iwai Tohnai
Maki Iwai
Masanari Umemura
Kenji Mitsudo
Source :
The journal of physiological sciences : JPS. 64(3)
Publication Year :
2014

Abstract

Hyperthermia is a promising anti-cancer treatment in which the tissue temperature is increased to 42-45 °C, and which is often used in combination with chemotherapy or radiation therapy. Our aim in the present work was to examine the feasibility of combination therapy for oral cancer with cisplatin and hyperthermia generated with ferucarbotran (Resovist(®); superparamagnetic iron oxide) in an alternating magnetic field (AMF). First, we established that administration of ferucarbotran at the approved dosage for magnetic resonance imaging provides an iron concentration sufficient to increase the temperature to 42.5 °C upon exposure to AMF. Then, we examined the effect of cisplatin combined with ferucarbotran/AMF-induced hyperthermia on cultured human oral cancer cells (HSC-3 and OSC-19). Cisplatin alone induced apoptosis of cancer cells in a dose-dependent manner, as is well known. However, the combination of cisplatin with ferucarbotran/AMF was significantly more effective than cisplatin alone. This result suggests that it might be possible to reduce the clinically effective dosage of cisplatin by administering it in combination with ferucarbotran/AMF-induced hyperthermia, thereby potentially reducing the incidence of serious cisplatin-related side effects. Further work seems justified to evaluate simultaneous thermo-chemotherapy as a new approach to anticancer therapy.

Details

ISSN :
18806562
Volume :
64
Issue :
3
Database :
OpenAIRE
Journal :
The journal of physiological sciences : JPS
Accession number :
edsair.doi.dedup.....551fc5537a81f4d632e8f617d496630a