BAG2 overexpression correlates with growth and poor prognosis of esophageal squamous cell carcinoma

Abstract: Previous studies have suggested that Bcl2-associated athanogene 2 (BAG2) serves as a crucial regulator for tumorigenesis in multiple tumors. However, little is known about the effect of BAG2 on esophageal squamous cell carcinoma (ESCC). This study focused on investigating whether BAG2 functions as a cancer-promoting gene in ESCC. In this work, gene expression data and clinical information from the NCBI Gene Expression Omnibus (GEO), Oncomine and The Cancer Genome Atlas (TCGA) were collected and analyzed. Expression of BAG2 in ESCC was determined using quantitative reverse transcription polymerase chain reaction (qRT-PCR). BAG2 was knocked down using small interference RNA (si-RNA) approach. Cell proliferation, migration and invasion were assessed by Cell Counting Kit-8 (CCK-8) and transwell assays. Molecular mechanism was detected by western blotting assay. The expression of BAG2 both in ESCC tissues and cells was upregulated and overexpression was associated with worsened prognosis. BAG2 silencing inhibited ESCC cell proliferation, migration and invasion, which was regulated by the phosphatidylinositol-3-kinase (PI3K)/protein kinase B (AKT) signaling pathway. These results reveal contributions of BAG2 as a predictor and potential therapeutic target in ESCC.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
BAG2 overexpression correlates with growth and poor prognosis of esophageal squamous cell carcinoma ; volume:13 ; number:1 ; year:2018 ; pages:582-588 ; extent:7
Open life sciences ; 13, Heft 1 (2018), 582-588 (gesamt 7)

Creator
Hong, Ying-Cai
Wang, Zheng
Peng, Bin
Xia, Li-Gang
Lin, Lie-Wen
Xu, Zheng-Lei

DOI
10.1515/biol-2018-0069
URN
urn:nbn:de:101:1-2409201646555.895642344756
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:39 AM CEST

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Associated

  • Hong, Ying-Cai
  • Wang, Zheng
  • Peng, Bin
  • Xia, Li-Gang
  • Lin, Lie-Wen
  • Xu, Zheng-Lei

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