1. SMPD3-mediated extracellular vesicle biogenesis inhibits oligodendroglioma growth
- Author
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Ahmed El-Sehemy, Yacine Touahri, Myra J. Chen, Thomas Olender, Carol Schuurmans, Cindi M. Morshead, Taylor Fleming, Jennifer A. Chan, Dawn Zinyk, Sajeevan Sujanthan, Shiekh Tanveer Ahmad, Valerie A. Wallace, Rehnuma Islam, Oleksandr Prokopchuk, Lata Adnani, Vorapin Chinchalongporn, Lacrimioara Comanita, Hon Leong, Marjorie Brand, Lakshmy Vasan, Anjali Balakrishnan, and Boris Kan
- Subjects
Chemistry ,Cell growth ,Cell ,Extracellular vesicle ,medicine.disease ,nervous system diseases ,Cell biology ,medicine.anatomical_structure ,Cell culture ,medicine ,TSG101 ,Cytotoxic T cell ,Oligodendroglioma ,neoplasms ,Cerebral organoid - Abstract
Oligodendrogliomas are lower-grade, slow-growing gliomas that are ultimately fatal. Although driver mutations are known, the mechanisms underlying their signature slow growth rates are poorly understood. We found evidence for intra-tumoral interactions between neoplastic and non-neoplastic cells in oligodendroglioma tissues. To further study these cell interactions, we used two patient-derived oligodendroglioma cell lines of lower and higher aggressivity. Both oligodendroglioma cell lines released extracellular vesicles that had cytotoxic effects on non-neoplastic and neoplastic cells, but each had distinct vesicular proteomes. Consistent with extracellular vesicles mediating growth inhibitory effects in oligodendrogliomas, higher expression levels of several extracellular vesicle biogenesis genes (SMPD3,TSG101, STAM1) correlates with longer survival in oligodendroglioma patients. Furthermore, SMPD3 overexpression slows oligodendroglioma cell growth in culture. Conversely, SMPD3 knockdown enhances oligodendroglioma proliferation in vitro, in murine xenografts, and in human cerebral organoid co-cultures. Oligodendroglioma-derived extracellular vesicles thus mediate tumor cell microenvironmental interactions that contribute to low aggressivity.
- Published
- 2020
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