| Literature DB >> 29667764 |
Chao Li1, Jingfang Zheng2, Si Chen1, Bin Huang1, Guosheng Li3, Zichao Feng4, Jiwei Wang4, Shujun Xu1.
Abstract
Glioblastoma pathogenesis is related to multiple processes that affected by dozens of regulatory factors, but the potential underlying factors regulating glioblastoma progression remains unclear. The goal of this research was to determine how the ribonucleotide reductase M2 subunit (RRM2) influenced proliferation, invasion, migration, and apoptosis of human glioblastoma cells. The level of proliferation of human glioblastoma cells was measured through CCK8, colony formation assay and immunofluorescence stains. Flow cytometry (FCM), wound healing, and transwell assays were conducted to detect cell apoptosis, migration, and invasion. Apoptotic level of cells and invasion-related expression of protein were measured by Western blot. Xenograft tumor model was established to confirm effect of RRM2 on the proliferation of human glioblastoma cells in vivo. Silencing RRM2 inhibited proliferation, invasion, and migration of glioblastoma cells whereas enhanced apoptosis rate. Overexpressing RRM2 promoted proliferation, migration and invasion but suppressed apoptosis. In vivo, Overexpressing RRM2 accelerated the tumor growth in glioblastoma cells. The present study illustrated that RRM2 was overexpressed in human glioblastoma cells. RRM2 promoted proliferation, migration, and invasion but inhibited apoptosis of human glioblastoma cells.Entities:
Keywords: RRM2; apoptosis; human glioblastoma; invasion; migration; proliferation
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Year: 2018 PMID: 29667764 DOI: 10.1002/jcp.26529
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384