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Biochemical and biophysical research communications, 2018-01, Vol.495 (1), p.446-453
2018
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Autor(en) / Beteiligte
Titel
GBP3 promotes glioma cell proliferation via SQSTM1/p62-ERK1/2 axis
Ist Teil von
  • Biochemical and biophysical research communications, 2018-01, Vol.495 (1), p.446-453
Ort / Verlag
United States: Elsevier Inc
Erscheinungsjahr
2018
Quelle
Elsevier ScienceDirect Journals
Beschreibungen/Notizen
  • Guanylate binding proteins (GBPs) are interferon-inducible large GTPases and play a crucial role in cell-autonomous immunity. However, the biology function of GBPs in cancer remains elusive. GBP3 is specifically expressed in adult brain. Here we show that GBP3 is highly elevated in human glioma tumors and glioma cell lines. Overexpression of GBP3 dramatically increased glioma cell proliferation whereas silencing GBP3 by RNA interference produced opposite effects. We further showed that GBP3 expression was able to induce sequestosome-1(SQSTM1, also named p62) expression and activate extracellular signal-regulated kinase (ERK1/2). The SQSTM1-ERK1/2 signaling cascade was essential for GBP3-promoted cell growth because depletion of SQSTM1 markedly reduced the phosphorylated ERK1/2 levels and GBP3-mediated cell growth, and inhibition of mitogen-activated protein kinase/ERK kinase abolished GBP3-induced glioma cell proliferation. Consistently, GBP3 overexpression significantly promoted glioma tumor growth in vivo and its expression was inversely correlated with the survival rate of glioma patients. Taken together, these results for the first time suggest that GBP3 contributes to the proliferation of glioma cells via regulating SQSTM1-ERK1/2 pathway, and GBP3 might represent as a new potential therapeutic target against glioma. •GBP3, an interferon-inducible large GTPase, is highly elevated in human glioma tumors.•GBP3 promotes glioma cell growth in vitro and in vivo through the SQSTM1/p62-ERK1/2 pathway.•GBP3 expression predicts poor outcome of glioma patients.
Sprache
Englisch
Identifikatoren
ISSN: 0006-291X
eISSN: 1090-2104
DOI: 10.1016/j.bbrc.2017.11.050
Titel-ID: cdi_osti_scitechconnect_23134491

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