| Literature DB >> 25832561 |
Feng Gu1, Huikun Zhang1, Fengxia Qin1, Xiaoli Liu1, Wenliang Li1, Li Fu1, Guoguang Ying1, Binghui Li1, Ming Zhang2, Yongjie Ma1.
Abstract
Glioblastomas, the most aggressive form of primary brain tumors with a tendency to invade surrounding healthy brain tissues, remains an incurable disease. Intersectin (ITSN) is a multidomain adapter protein implicated in endocytosis, exocytosis, and multiple signaling pathways. Prior research of ours has shown intersectin1-S (ITSN1-S) is critical for the migration and invasion of glioma cells by regulating several key proteins. In this study, we established ITSN1-S expression patterns in human tumor tissues. We discovered that ITSN1-S expression was positively correlated with histological grade of gliomas and with poor patient prognosis. We also found that the expression of ITSN1-S protein was essential to glioblastoma cell proliferation. Furthermore, through a series of expression constructs encoding different ITSN1-S domains, we identified the critical roles of ITSN1-S SH3 domains in the regulation of cell proliferation. This study also demonstrates evidence suggesting that the regulation of ITSN1-S on glioblastoma cells proliferation is through the Raf/MEK/ERK pathway. In conclusion, this study suggests critical roles of ITSN1-S in malignant glioma proliferation, indicating a potential usage of ITSN1-S in the therapeutic intervention as a novel molecular target.Entities:
Keywords: ITSN1 isoforms; ITSN1-S; SH3 domain; cell proliferation; glioblastoma; signaling pathway
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Year: 2015 PMID: 25832561 DOI: 10.1002/glia.22830
Source DB: PubMed Journal: Glia ISSN: 0894-1491 Impact factor: 7.452