Affordable Access

Access to the full text

ATF5 and HIF1α cooperatively activate HIF1 signaling pathway in esophageal cancer

Authors
  • He, Feng1
  • Xiao, Hang1
  • Cai, Yixin1
  • Zhang, Ni1
  • 1 Tongji Medical College Huazhong University of Science and Technology, Wuhan, 430030, China , Wuhan (China)
Type
Published Article
Journal
Cell Communication and Signaling
Publisher
BioMed Central
Publication Date
May 12, 2021
Volume
19
Issue
1
Identifiers
DOI: 10.1186/s12964-021-00734-x
Source
Springer Nature
Keywords
License
Green

Abstract

BackgroundEsophageal cancer (ESCA) is one of the most common cancers worldwide and has a very poor prognosis. Hypoxia-inducible factor 1 (HIF1) signaling pathway plays a critical role in tumorigenesis and is therefore considered a potential therapeutic target in the treatment of many cancers. Activating transcription factor 5 (ATF5) facilitates the expression of various genes and has been extensively studied for its potential role in cancer treatment.MethodsThe expression level of ATF5 in clinic sample was detected by quantitative real time PCR and immunohistochemistry. ATF5 biological function was investigated by western blot, cell cycle analysis, cell viability assay, luciferase reporter assays, colony formation assay, transwell assay, wound healing assay, tube formation assay, and ELISA assay. CHIP and Re-CHIP assay, GST-pulldown, and RNA-sequencing were used to study the cross-talks between ATF5 and HIF1 complex. Mouse xenograft study was utilized to study the correlation of ATF5 and tumor growth in vivo. Student’s t-test or Chi-square test was used for statistical analysis.ResultsHere, we first found ATF5 was dramatically upregulated in ESCA cancer and related with poor survival time. Next, we found that the expression level of ATF5 had a positive relationship with the proliferation, migration, and invasion ability of ESCA cells. Besides, we innovatively found that ATF5 functions as a novel coactivator in HIF1 transcription complex by binding to HIF1α. Further, we demonstrated that silencing ATF5 phenocopies HIF1α knockdown in tumorigenic properties in vitro and inhibited ESCA tumor angiogenesis and proliferation in vivo.ConclusionHerein, we found ATF5 as a novel component of the HIF1 transcription complex. The findings of the present study may provide new insights into the development of a novel and more efficient therapeutic strategy against ESCA.AdnowYwCvGQPELyR7fEPboVideo abstract

Report this publication

Statistics

Seen <100 times