Oncotarget

Research Papers:

Slowing down glioblastoma progression in mice by running or the anti-malarial drug dihydroartemisinin? Induction of oxidative stress in murine glioblastoma therapy

Dieter Lemke, Hans-Werner Pledl, Markus Zorn, Manfred Jugold, Ed Green, Jonas Blaes, Sarah Löw, Anne Hertenstein, Martina Ott, Felix Sahm, Ann-Catherine Steffen, Markus Weiler, Frank Winkler, Michael Platten, Zhen Dong _ and Wolfgang Wick

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Oncotarget. 2016; 7:56713-56725. https://doi.org/10.18632/oncotarget.10723

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Abstract

Dieter Lemke1,2,3, Hans-Werner Pledl1,2,3, Markus Zorn4, Manfred Jugold5, Ed Green1,6, Jonas Blaes1,2, Sarah Löw1,2,3, Anne Hertenstein1,2,3, Martina Ott1,6, Felix Sahm1,7,8, Ann-Catherine Steffen1,2, Markus Weiler1,2,3, Frank Winkler1,2,3, Michael Platten1,3,6, Zhen Dong9,*, Wolfgang Wick1,2,3,*

1German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany

2Clinical Cooperation Unit Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany

3Neurology Clinic and National Center for Tumor Diseases, University of Heidelberg, German Cancer Research Center (DKFZ), Heidelberg, Germany

4Central Laboratory of Heidelberg University Hospital, German Cancer Research Center (DKFZ), Heidelberg, Germany

5Core Facility Small Animal Imaging Center, German Cancer Research Center (DKFZ), Heidelberg, Germany

6Clinical Cooperation Unit Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany

7Department of Neuropathology, Institute of Pathology, University of Heidelberg, German Cancer Research Center (DKFZ), Heidelberg, Germany

8Clinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg, Germany

9Department of Neurosurgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

*These authors have shared senior authorship

Correspondence to:

Zhen Dong, email: dongz@tjh.tjmu.edu.cn

Wolfgang Wick, email: wolfgang.wick@med.uni-heidelberg.de

Keywords: dihydroartemisinin, glioblastoma, physical exercises (PE), therapy, physical exercise

Received: May 11, 2016     Accepted: June 14, 2016     Published: July 20, 2016

ABSTRACT

Influencing cancer metabolism by lifestyle changes is an attractive strategy as - if effective - exercise-induced problems may be less severe than those induced by classical anti-cancer therapies. Pursuing this idea, clinical trials evaluated the benefit of e.g. different diets such as the ketogenic diet, intermittent caloric restriction and physical exercise (PE) in the primary and secondary prevention of different cancer types. PE proved to be beneficial in the context of breast and colon cancer.

Glioblastoma has a dismal prognosis, with an average overall survival of about one year despite maximal safe resection, concomitant radiochemotherapy with temozolomide followed by adjuvant temozolomide therapy. Here, we focused on the influence of PE as an isolated and adjuvant treatment in murine GB therapy.

PE did not reduce toxic side effects of chemotherapy in mice administered in a dose escalating scheme as shown before for starvation. Although regular treadmill training on its own had no obvious beneficial effects, its combination with temozolomide was beneficial in the treatment of glioblastoma-bearing mice. As PE might partly act through the induction of reactive oxygen species, dihydroartemisinin - an approved anti-malarial drug which induces oxidative stress in glioma cells - was further evaluated in vitro and in vivo. Dihydroartemisinin showed anti-glioma activity by promoting autophagy, reduced the clonogenic survival and proliferation capacity of glioma cells, and prolonged the survival of tumor bearing mice. Using the reactive oxygen species scavenger n-acetyl-cysteine these effects were in part reversible, suggesting that dihydroartemisinin partly acts through the generation of reactive oxygen species.


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