Mechanical nanosurgery of chemoresistant glioblastoma using magnetically controlled carbon nanotubes

Author:

Wang Xian12ORCID,Gong Zheyuan3ORCID,Wang Tiancong3ORCID,Law Junhui3ORCID,Chen Xin124ORCID,Wanggou Siyi1256,Wang Jintian3ORCID,Ying Binbin3ORCID,Francisco Michelle12ORCID,Dong Weifan127ORCID,Xiong Yi1256ORCID,Fan Jerry J.127ORCID,MacLeod Graham8ORCID,Angers Stephane8910ORCID,Li Xuejun56ORCID,Dirks Peter B.127ORCID,Liu Xinyu3,Huang Xi127ORCID,Sun Yu3111213ORCID

Affiliation:

1. Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, ON, Canada.

2. Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, ON, Canada.

3. Department of Mechanical and Industrial Engineering, University of Toronto, Toronto, ON, Canada.

4. Songjiang Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.

5. Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.

6. Hunan International Scientific and Technological Cooperation Base of Brain Tumor Research, Xiangya Hospital, Central South University, Changsha, Hunan, China.

7. Department of Molecular Genetics, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

8. Donnelly Centre for Cellular & Biomolecular Research, University of Toronto, Toronto, ON, Canada.

9. Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, ON, Canada.

10. Department of Biochemistry, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

11. Institute of Biomedical Engineering, University of Toronto, Toronto, ON, Canada.

12. Department of Electrical and Computer Engineering, University of Toronto, Toronto, ON, Canada.

13. Department of Computer Science, University of Toronto, Toronto, ON, Canada.

Abstract

Glioblastoma (GBM) is the most common and aggressive primary brain cancer. Despite multimodal treatment including surgery, radiotherapy, and chemotherapy, median patient survival has remained at ~15 months for decades. This situation demands an outside-the-box treatment approach. Using magnetic carbon nanotubes (mCNTs) and precision magnetic field control, we report a mechanical approach to treat chemoresistant GBM. We show that GBM cells internalize mCNTs, the mobilization of which by rotating magnetic field results in cell death. Spatiotemporally controlled mobilization of intratumorally delivered mCNTs suppresses GBM growth in vivo. Functionalization of mCNTs with anti-CD44 antibody, which recognizes GBM cell surface–enriched antigen CD44, increases mCNT recognition of cancer cells, prolongs mCNT enrichment within the tumor, and enhances therapeutic efficacy. Using mouse models of GBM with upfront or therapy-induced resistance to temozolomide, we show that mCNT treatment is effective in treating chemoresistant GBM. Together, we establish mCNT-based mechanical nanosurgery as a treatment option for GBM.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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