4.3 Article

HOXA13 is a potential GBM diagnostic marker and promotes glioma invasion by activating the Wnt and TGF-β pathways

Journal

ONCOTARGET
Volume 6, Issue 29, Pages 27778-27793

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.4813

Keywords

Homeobox (HOX) gene; HOXA13; glioma; smad; epithelial-to-mesenchymal transition (EMT)

Funding

  1. National High Technology Research and Development Program 863 [2014AA021102, 2012AA02A508]
  2. China National Natural Scientific Fund [81372703]
  3. Natural Science Foundation of Tianjin Municipal Science and Technology Commission [12ZCDZSY17300]

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Homeobox ( HOX) genes, including HOXA13, are involved in human cancer. We found that HOXA13 expression was associated with glioma grade and prognosis. Bioinformatics analysis revealed that most of the HOXA13-associated genes were enriched in cancer-related signaling pathways and mainly involved in the regulation of transcription. We transfected four glioma cell lines with Lenti-si HOXA13. HOXA13 increased cell proliferation and invasion and inhibited apoptosis. HOXA13 decreased beta-catenin, phospho-smad2, and phospho-smad3 in the nucleus and increased phospho-beta-catenin in the cytoplasm. Furthermore, downregulation of HOXA13 in orthotopic tumors decreased tumor growth. We suggest that HOXA13 promotes glioma progression in part via Wnt- and TGF-beta-induced EMT and is a potential diagnostic biomarker for glioblastoma and an independent prognostic factor in high-grade glioma.

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