دورية أكاديمية

CD44v6 Regulates Growth of Brain Tumor Stem Cells Partially through the AKT-Mediated Pathway.

التفاصيل البيبلوغرافية
العنوان: CD44v6 Regulates Growth of Brain Tumor Stem Cells Partially through the AKT-Mediated Pathway.
المؤلفون: Jijiwa, Mayumi1, Demir, Habibe1, Gupta, Snehalata1, Leung, Crystal2, Joshi, Kaushal1, Orozco, Nicholas3, Huang, Tiffany4, Yildiz, Vedat O.5, Shibahara, Ichiyo3, de Jesus, Jason A.4, Yong, William H.4, Mischel, Paul S.4, Fernandez, Soledad5, Kornblum, Harley I.2,3, Nakano, Ichiro1,6 ichiro.nakano@osumc.edu
المصدر: PLoS ONE. 2011, Vol. 6 Issue 9, p1-12. 12p.
مصطلحات موضوعية: *GENETIC regulation, *BRAIN tumors, *TUMOR growth, *STEM cells, *PROTEIN kinase B regulation, *OSTEOPONTIN, *SMALL interfering RNA, *GLIOBLASTOMA multiforme
مستخلص: Identification of stem cell-like brain tumor cells (brain tumor stem-like cells; BTSC) has gained substantial attention by scientists and physicians. However, the mechanism of tumor initiation and proliferation is still poorly understood. CD44 is a cell surface protein linked to tumorigenesis in various cancers. In particular, one of its variant isoforms, CD44v6, is associated with several cancer types. To date its expression and function in BTSC is yet to be identified. Here, we demonstrate the presence and function of the variant form 6 of CD44 (CD44v6) in BTSC of a subset of glioblastoma multiforme (GBM). Patients with CD44high GBM exhibited significantly poorer prognoses. Among various variant forms, CD44v6 was the only isoform that was detected in BTSC and its knockdown inhibited in vitro growth of BTSC from CD44high GBM but not from CD44low GBM. In contrast, this siRNA-mediated growth inhibition was not apparent in the matched GBM sample that does not possess stem-like properties. Stimulation with a CD44v6 ligand, osteopontin (OPN), increased expression of phosphorylated AKT in CD44high GBM, but not in CD44low GBM. Lastly, in a mouse spontaneous intracranial tumor model, CD44v6 was abundantly expressed by tumor precursors, in contrast to no detectable CD44v6 expression in normal neural precursors. Furthermore, overexpression of mouse CD44v6 or OPN, but not its dominant negative form, resulted in enhanced growth of the mouse tumor stem-like cells in vitro. Collectively, these data indicate that a subset of GBM expresses high CD44 in BTSC, and its growth may depend on CD44v6/AKTpathway. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:19326203
DOI:10.1371/journal.pone.0024217