Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/78004
Title: Musashi-1 promotes chemoresistant granule formation by PKR/eIF2α signalling cascade in refractory glioblastoma
Authors: Chen, HY
Lin, LT 
Wang, ML
Tsai, KL
Huang, PI
Yang, YP
Lee, YY
Chen, YW
Lo, WL
Lan, YT
Chiou, SH
Lin, CM
Ma, HI
Chen, MT
Keywords: Drug resistance
Glioblastoma multiforme
Musashi-1
PKR
Stress granule
Issue Date: 2018
Publisher: Elsevier
Source: Biochimica et biophysica acta. Molecular basis of disease, 2018, v. 1864, no. 5, p. 1850-1861 How to cite?
Journal: Biochimica et biophysica acta. Molecular basis of disease 
Abstract: Musashi-1 (MSI1), one of the RNA-binding proteins, is abundantly found not only in neural stem cells but also in several cancer tissues and has been reported to act as a positive regulator of cancer progression. Growing evidence indicates that PKR and eIF2α play pivotal roles in the stimulation of stress granule formation as well as in the subsequent translation modulation in response to stressful conditions; however, little is known about whether MSI1 is involved in this PKR/eIF2α cancer stem cell-enhancing machinery. In this study, we demonstrated that MSI1 promotes human glioblastoma multiforme (GBM) stem cells and enhances chemoresistance when exposed to sublethal stress. The overexpression of MSI1 leads to a protective effect in mitigating drug-induced cell death, thus facilitating the formation of chemoresistant stress granules (SGs) in response to arsenic trioxide (ATO) treatment. SG components, such as PKR and eIF2α, were dominantly activated and assembled, while ATO was engaged. The activated PKR and eIF2α contribute to the downstream enhancement of stem cell genes, thereby promoting the progression of GBM. The silencing of MSI1 or PKR both obviously withdrew the phenomena. Taken together, our findings indicate that MSI1 plays a leading role in stress granule formation that grants cancer stem cell properties and chemoresistant stress granules in GBM, in response to stressful conditions via the PKR/eIF2α signalling cascade.
URI: http://hdl.handle.net/10397/78004
ISSN: 0925-4439
DOI: 10.1016/j.bbadis.2018.02.017
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