| Literature DB >> 32575464 |
Kirsten Strømme Kierulf-Vieira1,2,3, Cecilie Jonsgar Sandberg1,2, Jo Waaler4,5, Kaja Lund4,5, Erlend Skaga1,2,3, Birthe Mikkelsen Saberniak1,2, Ioannis Panagopoulos6, Petter Brandal6,7,8, Stefan Krauss4,5, Iver Arne Langmoen1,2,3,8,9, Einar Osland Vik-Mo1,2,3,8,9.
Abstract
Evidence suggests that the growth and therapeutic resistance of glioblastoma (GBM) may be enabled by a population of glioma stem cells (GSCs) that are regulated by typical stem cell pathways, including the WNT/β-catenin signaling pathway. We wanted to explore the effect of treating GSCs with a small-molecule inhibitor of tankyrase, G007-LK, which has been shown to be a potent modulator of the WNT/β-catenin and Hippo pathways in colon cancer. Four primary GSC cultures and two primary adult neural stem cell cultures were treated with G007-LK and subsequently evaluated through the measurement of growth characteristics, as well as the expression of WNT/β-catenin and Hippo signaling pathway-related proteins and genes. Treatment with G007-LK decreased in vitro proliferation and sphere formation in all four primary GSC cultures in a dose-dependent manner. G007-LK treatment altered the expression of key downstream WNT/β-catenin and Hippo signaling pathway-related proteins and genes. Finally, cotreatment with the established GBM chemotherapeutic compound temozolomide (TMZ) led to an additive reduction in sphere formation, suggesting that WNT/β-catenin signaling may contribute to TMZ resistance. These observations suggest that tankyrase inhibition may serve as a supplement to current GBM therapy, although more work is needed to determine the exact downstream mechanisms involved.Entities:
Keywords: Hippo; WNT; glioblastoma; glioma stem cells; tankyrase; temozolomide; β-catenin
Year: 2020 PMID: 32575464 DOI: 10.3390/cancers12061630
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639