Home > Journals > Journal of Neurosurgical Sciences > Past Issues > Journal of Neurosurgical Sciences 2023 August;67(4) > Journal of Neurosurgical Sciences 2023 August;67(4):422-30

CURRENT ISSUE
 

JOURNAL TOOLS

Publishing options
eTOC
To subscribe
Submit an article
Recommend to your librarian
 

ARTICLE TOOLS

Publication history
Reprints
Permissions
Cite this article as
Share

 

ORIGINAL ARTICLE   

Journal of Neurosurgical Sciences 2023 August;67(4):422-30

DOI: 10.23736/S0390-5616.20.05107-3

Copyright © 2020 EDIZIONI MINERVA MEDICA

language: English

Early growth response 1 promoted the invasion of glioblastoma multiforme by elevating HMGB1

Kai DU 1, Xiaoyou WU 2, Xiaofei JI 2, Nan LIANG 3, Zheng LI 3

1 Department of Neurosurgery, Yidu Central Hospital of Weifang, Weifang, China; 2 Department of Pediatrics, Yidu Central Hospital of Weifang, Weifang, China; 3 Department of Neurosurgery, the Second Hospital of Shandong First Medical University, Taian, China



BACKGROUND: Glioblastoma multiforme (GBM) is the most common and deadly glioma subtype. Early growth response 1 (EGR1) participates in the progression of several cancer types, but the expression and function of EGR1 in GBM was rarely investigated.
METHODS: The expressions of EGR1 in GBM were detected with qRT-PCR and immunohistochemistry in 12 pairs of fresh GBM tissues and 116 paraffin-embedded specimens. The patients were divided into high and low EGR1 groups according to the IHC score of EGR1, and the prognostic significances of different groups were evaluated with univariate and multivariate analyses. With in-vitro experiments, we assessed the role of EGR1 in the proliferation and invasion of GBM cells.
RESULTS: In our study, EGR1 was up-regulated in GBM tissues compared with tumor-adjacent normal tissues. High expression of EGR1 or HMGB1 were unfavorable prognostic biomarkers of GBM. Coexpression of EGR1 and HMGB1 could predict the prognosis of GBM more sensitively. EGR1 facilitated the proliferation and invasion of GBM cells. Moreover, EGR1 promoted the invasion, instead of proliferation, of GBM cells by elevating the expression of HMGB1.
CONCLUSIONS: ERG1 was a prognostic biomarker of GBM, and ERG1 and HMGB1 synergistically could predict the GBM prognosis more precisely. ERG1 could promote GBM cell invasion by inducing HMGB1 expression.


KEY WORDS: Glioblastoma; Early growth response protein 1; Prognosis

top of page