Correlation Engine 2.0
Clear Search sequence regions


  • apoptosis (1)
  • cancers (3)
  • cell cycle (1)
  • factors (2)
  • gene (1)
  • glioma (14)
  • glioma brain (1)
  • heart (14)
  • humans (1)
  • lbh protein, human (1)
  • limb- bud (14)
  • patients (1)
  • protein human (1)
  • Sizes of these terms reflect their relevance to your search.

    Glioma is the predominant brain malignancy and is correlated with high mortality and severe morbidity. The transcription factor limb-bud and heart (LBH) has been reported to be involved in the development of several cancers, although its role in glioma development remains elusive. Here, we examined the effect of LBH on glioma progression. The expression of LBH was increased in glioma samples from The Cancer Genome Atlas database, and upregulation of LBH was observed to be correlated with the poor survival of glioma patients. We also report that expression of LBH was elevated in clinical glioma tissues compared to adjacent normal tissues, and was also enhanced in glioma cell lines. LBH promotes proliferation and inhibits cell cycle arrest and apoptosis in glioma cells. In addition, LBH increased the migration and invasion of glioma cells in vitro. Moreover, tumorigenicity analysis revealed that LBH could promote the tumor growth of glioma cells in vivo. In conclusion, our findings suggest that LBH contributes to glioma progression in vitro and in vivo. Our findings provide new insights into the mechanism by which LBH promotes the development of glioma, improving our understanding of the correlation between LBH with cancer. LBH may have potential as a target for glioma therapy. © 2021 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.

    Citation

    Luotong Liu, Qinglian Luo, Qian Xu, Yu Xiong, Huajiang Deng. Limb-bud and heart development (LBH) contributes to glioma progression in vitro and in vivo. FEBS open bio. 2022 Jan;12(1):211-220

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 34739189

    View Full Text