Electro-hyperthermia inhibits glioma tumorigenicity through the induction of E2F1-mediated apoptosis. (3rd October 2015)

• Record Type: Journal Article
• Authors: Cha, Jihye; Jeon, Tae-Won; Lee, Chang Geol; Oh, Sang Taek; Yang, Hee-Beom; Choi, Kyung-Ju; Seo, Daekwan; Yun, Ina; Baik, In Hye; Park, Kyung Ran; Park, Young Nyun; Lee, Yun-Han
• Is Part Of: International journal of hyperthermia. Volume 31:Number 7(2015)
• Page Start: 784
• Page End: 792
• Publication Date: 2015-10-03
• Subjects: Apoptosis -- cancer stem cells -- electro-hyperthermia -- E2F1 -- glioma; Thermotherapy -- Periodicals; 615.832
• DOI: 10.3109/02656736.2015.1069411
• Languages: English
• ISSNs: 0265-6736

Abstract

Abstract: Purpose : Modulated electro-hyperthermia (mEHT), also known as oncothermia, shows remarkable treatment efficacies for various types of tumours, including glioma. The aim of the present study was to investigate the molecular mechanism underlying phenotypic changes in oncothermic cancer cells. Materials and methods : U87-MG and A172 human glioma cells were exposed to mEHT (42 °C/60 min) three times with a 2-day interval and subsequently tested for growth inhibition using MTS, FACS and microscopic analysis. To obtain insights into the molecular changes in response to mEHT, global changes in gene expression were examined using RNA sequencing. For in vivo evaluation of mEHT, we used U87-MG glioma xenografts grown in nude mice. Results : mEHT inhibited glioma cell growth through the strong induction of apoptosis. The transcriptomic analysis of differential gene expression under mEHT showed that the anti-proliferative effects were induced through a subset of molecular alterations, including the up-regulation of E2F1 and CPSF2 and the down-regulation of ADAR and PSAT1. Subsequent Western blotting revealed that mEHT increased the levels of E2F1 and p53 and decreased the level of PARP-1, accelerating apoptotic signalling in glioma cells. mEHT significantly suppressed the growth of human glioma xenografts in nude mice. We also observed that mEHT dramatically reduced the portion of CD133 + glioma stem cell population and suppressed cancer cell migration and sphere formation. Conclusions : These findings suggest that mEHT suppresses glioma cell proliferation and mobility through the induction of E2F1-mediated apoptosis and might be an effective treatment for eradicating brain tumours.