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Expression, Prognosis, and Immune Infiltrates Analyses of E2F-Related Transcription Factor Family in Human Brain and CNS Cancer

33 Pages Posted: 25 Jun 2020

See all articles by Pan Liao

Pan Liao

Department of Neurology, Inner Mongolia Forestry General Hospital

Shuzhen Han

Inner Mongolia Forestry General Hospital - Department of Neurology

Honglan Qu

Inner Mongolia Forestry General Hospital - Department of Oncology

More...

Abstract

Background: We investigated the expression patterns, potential functions, unique prognostic value, and potential therapeutic targets of E2Fs in brain and CNS cancer and tumor-infiltrating immune cell microenvironments.

Methods: We analyzed E2Fs mRNA expression levels in diverse cancer types via Oncomine and GEPIA databases and diverse cancer cell lines via CCLE and EMBL-EBI databases, respectively. Furthermore, we evaluated the prognostic values using GEPIA database and the correlation of E2Fs expression with the abundance of immune infiltrates and the correlation between immune cell infiltration and GBM and LGG prognosis via TIMER database.

Findings: E2F1–8 expressions increased in most cancers compared with normal tissues, especially in brain and CNS cancer. E2F1–8 were highly expressed in most cancer cell lines, particularly neuroblastomas and gliomas. The higher expression of E2F1, -2, -4, -6, -7, and 8 indicated poor overall survival, and that of E2F2, -4, -7, and -8 indicated poor disease-free survival (both, p < 0·05) of all patients with LGG, but no significant correlation was found in GBM patients. Increased E2F3–6 and E2F1–8 expressions correlated with poor prognosis and increased immune infiltration levels in CD8+ T-cells, macrophages, neutrophils, and DCs in GBM and B-cells, CD8+ T-cells, CD4+ T-cells, macrophages, neutrophils, and DCs in LGG, respectively.

Interpretation: The E2F family showed significant expression differences between brain and CNS cancer and normal tissues. E2F1–8 and E2F2–8 could be hopeful prognostic biomarkers for GBM, and LGG, respectively. E2F3–6 and E2F1–8 could be likely therapeutic targets in patients with immune cell infiltration of GBM and LGG, respectively.

Funding Statement: No source of funding.

Declaration of Interests: No conflict of interest.

Keywords: Therapeutic target; Prognosis biomarker; Immune infiltrates; E2Fs; Brain and CNS cancer

Suggested Citation

Liao, Pan and Han, Shuzhen and Qu, Honglan, Expression, Prognosis, and Immune Infiltrates Analyses of E2F-Related Transcription Factor Family in Human Brain and CNS Cancer (4/3/2020). Available at SSRN: https://ssrn.com/abstract=3569825 or http://dx.doi.org/10.2139/ssrn.3569825

Pan Liao

Department of Neurology, Inner Mongolia Forestry General Hospital

United States

Shuzhen Han

Inner Mongolia Forestry General Hospital - Department of Neurology ( email )

Yakeshi
China

Honglan Qu (Contact Author)

Inner Mongolia Forestry General Hospital - Department of Oncology ( email )

Yakeshi
China

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