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CANCER STEM CELLS |
1 Maxine-Dunitz Neurosurgical Institute, Suite 800 East, 8631 West 3rd Street, Los Angeles, CA 90048
2 Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA 90048
* To whom correspondence should be addressed. E-mail: Yuj{at}cshs.org.
| Abstract |
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The rat 9L gliosarcoma is a widely used syngeneic rat brain tumor model that closely simulates glioblastoma multiforme (GBM) when implanted in vivo. In this study, we sought to isolate and characterize a subgroup of cancer stem-like cells (CSLCs) from the 9L gliosarcoma cell line, which may represent the tumor initiating subpopulation of cells. We demonstrate that these CSLCs form clonal derived spheres in media devoid of serum supplemented with mitogens EGF and bFGF, express the neural stem cell (NSC) markers Nestin and Sox2, self-renew, and differentiate into neuron-like and glial cells in vitro. More importantly, these cells can propagate and recapitulate tumors when implanted into the brain of syngeneic Fisher rats, and display a more aggressive course when compared to 9L gliosarcoma grown in monolayer cultures devoid of mitogens. Furthermore, we compare the chemosensitivity and proliferation rate of 9L gliosarcoma cells grown as monolayer to those grown as floating spheres and show that the sphere generated cells have a lower proliferation rate, are more chemoresistant, and express several anti-apoptosis and drug related genes, which may prove to have important clinical implications.
Key Words. Spheres, Monolayer, Mitogens, Cancer Stem-Like Cells (CSLCs),, Glioma
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