| Literature DB >> 33718179 |
Chenghao Peng1,2, Hanmin Chen1, Youwei Li1, Hang Yang3, Peizhong Qin4, Baojun Ma5, Qiuhong Duan2, Baofeng Wang1, Feng Mao1, Dongsheng Guo1.
Abstract
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.Entities:
Keywords: LRIG3; PI3K/AKT; angiogenesis; glioma; vascular endothelial growth factor A
Year: 2021 PMID: 33718179 PMCID: PMC7946980 DOI: 10.3389/fonc.2021.621154
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244