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Silencing of R-Spondin1 increases radiosensitivity of glioma cells.

Oncotarget (2015-04-14)
Xuefeng Gu, Xuefeng Wang, Hong Xiao, Guoda Ma, Lili Cui, You Li, Haihong Zhou, Wandong Liang, Bin Zhao, Keshen Li
RESUMEN

Although radiation therapy is the most effective postoperative adjuvant treatment, it does not substantially improve the long-term outcomes of glioma patients because of the characteristic radioresistance of glioma. We found that R-Spondin1 (Rspo1) expression was elevated in high-grade gliomas and was associated with worse overall survival and disease-free survival. Rspo1 expression was also associated with reduced survival rates in glioma patients after treatment with radiotherapy and temozolomide (RT-TMZ). Importantly, Rspo1 was dramatically upregulated after radiation treatment in patients with glioma. Rspo1 silencing by shRNA potentiated glioma cell death upon radiation treatment. In a xenograft nude mouse model, combining radiation and silencing of Rspo1 potentiated tumor growth inhibition. Thus, combining radiotherapy with silencing of Rspo1 is a potential therapeutic approach.

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Sigma-Aldrich
R-SPONDIN-1 human, recombinant, expressed in CHO cells, ≥95% (SDS-PAGE), ≥95% (HPLC)