Frontiers in Oncology (Feb 2021)

LRIG3 Suppresses Angiogenesis by Regulating the PI3K/AKT/VEGFA Signaling Pathway in Glioma

  • Chenghao Peng,
  • Chenghao Peng,
  • Hanmin Chen,
  • Youwei Li,
  • Hang Yang,
  • Peizhong Qin,
  • Baojun Ma,
  • Qiuhong Duan,
  • Baofeng Wang,
  • Feng Mao,
  • Dongsheng Guo

DOI
https://doi.org/10.3389/fonc.2021.621154
Journal volume & issue
Vol. 11

Abstract

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High levels of microvessel density (MVD) indicate poor prognosis in patients with malignant glioma. Leucine-rich repeats and immunoglobulin-like domains (LRIG) 3, a potential tumor suppressor, plays an important role in tumor progression and may serve as a biomarker in many human cancers. However, its role and underlying mechanism of action in glioma angiogenesis remain unclear. In the present study, we used loss- and gain-of-function assays to show that LRIG3 significantly suppressed glioma-induced angiogenesis, both in vitro and in vivo. Mechanistically, LRIG3 inhibited activation of the PI3K/AKT signaling pathway, downregulating vascular endothelial growth factor A (VEGFA) in glioma cells, thereby inhibiting angiogenesis. Notably, LRIG3 had a significant negative correlation with VEGFA expression in glioma tissues. Taken together, our results suggest that LRIG3 is a novel regulator of glioma angiogenesis and may be a promising option for developing anti-angiogenic therapy.

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