Regulation of Glioblastoma Tumor-Propagating Cells by the Integrin Partner Tetraspanin CD151
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- 作者：Jessica Tilghman* ; &dagger ; ; Paula Schiapparelli&Dagger ; ; Bachuchu Lal* ; § ; ; Mingyao Ying* ; § ; ; Alfredo Quinones-Hinojosa&dagger ; ; &Dagger ; ; ¶ ; ; Shuli Xia* ; § ; ; John Laterra* ; &dagger ; ; § ; ; ¶ ; ; laterra@kennedykrieger.org" class="auth_mail" title="E-mail the corresponding author
- 刊名：Neoplasia
- 出版年：2016
- 出版时间：March 2016
- 年：2016
- 卷：18
- 期：3
- 页码：185-198
- 全文大小：2178 K
文摘
Glioblastoma (GBM) stem cells (GSCs) represent tumor-propagating cells with stem-like characteristics (stemness) that contribute disproportionately to GBM drug resistance and tumor recurrence. Understanding the mechanisms supporting GSC stemness is important for developing therapeutic strategies for targeting GSC-dependent oncogenic mechanisms. Using GBM-derived neurospheres, we identified the cell surface tetraspanin family member CD151 as a novel regulator of glioma cell stemness, GSC self-renewal capacity, migration, and tumor growth. CD151 was found to be overexpressed in GBM tumors and GBM neurospheres enriched in GSCs. Silencing CD151 inhibited neurosphere forming capacity, neurosphere cell proliferation, and migration and attenuated the expression of markers and transcriptional drivers of the GSC phenotype. Conversely, forced CD151 expression promoted neurosphere self-renewal, cell migration, and expression of stemness-associated transcription factors. CD151 was found to complex with integrins α3, α6, and β1 in neurosphere cells, and blocking CD151 interactions with integrins α3 and α6 inhibited AKT phosphorylation, a downstream effector of integrin signaling, and impaired sphere formation and neurosphere cell migration. Additionally, targeting CD151 in vivo inhibited the growth of GBM neurosphere-derived xenografts. These findings identify CD151 and its interactions with integrins α3 and α6 as potential therapeutic targets for inhibiting stemness-driving mechanisms and stem cell populations in GBM.