Notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cells
Abstract Background Hemangiosarcoma (HSA) is a malignant tumor derived from endothelial cells which usually shows poor prognosis due to its high invasiveness, metastatic rate and severe hemorrhage from tumor ruptures. Since the pathogenesis of HSA is not yet complete, further understanding of its mo...
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doaj-b17f41bc7745495aa87a3451f4072fca2020-11-24T20:42:49ZengBMCBMC Veterinary Research1746-61482018-10-0114111610.1186/s12917-018-1624-8Notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cellsKeisuke Aoshima0Yuki Fukui1Kevin Christian Montecillo Gulay2Ochbayar Erdemsurakh3Atsuya Morita4Atsushi Kobayashi5Takashi Kimura6Laboratory of Comparative Pathology, Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido UniversityLaboratory of Comparative Pathology, Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido UniversityLaboratory of Comparative Pathology, Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido UniversityLaboratory of Comparative Pathology, Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido UniversityLaboratory of Comparative Pathology, Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido UniversityLaboratory of Comparative Pathology, Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido UniversityLaboratory of Comparative Pathology, Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido UniversityAbstract Background Hemangiosarcoma (HSA) is a malignant tumor derived from endothelial cells which usually shows poor prognosis due to its high invasiveness, metastatic rate and severe hemorrhage from tumor ruptures. Since the pathogenesis of HSA is not yet complete, further understanding of its molecular basis is required. Results Here, we identified Notch2 signal as a key factor in maintaining canine HSA cancer stem cell (CSC)-like cells. We first cultured HSA cell lines in adherent serum-free condition and confirmed their CSC-like characteristics. Notch signal was upregulated in the CSC-like cells and Notch signal inhibition by a γ-secretase inhibitor significantly repressed their growth. Notch2, a Notch receptor, was highly expressed in the CSC-like cells. Constitutive activation of Notch2 increased clonogenicity and number of cells which were able to survive in serum-free condition. In contrast, inhibition of Notch2 activity showed opposite effects. These results suggest that Notch2 is an important factor for maintaining HSA CSC-like cells. Neoplastic cells in clinical cases also express Notch2 higher than endothelial cells in the normal blood vessels in the same slides. Conclusion This study provides foundation for further stem cell research in HSA and can provide a way to develop effective treatments to CSCs of endothelial tumors.http://link.springer.com/article/10.1186/s12917-018-1624-8Cancer stem cell-like cellsHemangiosarcomaNotch2OncologyTumor Biology |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Keisuke Aoshima Yuki Fukui Kevin Christian Montecillo Gulay Ochbayar Erdemsurakh Atsuya Morita Atsushi Kobayashi Takashi Kimura |
spellingShingle |
Keisuke Aoshima Yuki Fukui Kevin Christian Montecillo Gulay Ochbayar Erdemsurakh Atsuya Morita Atsushi Kobayashi Takashi Kimura Notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cells BMC Veterinary Research Cancer stem cell-like cells Hemangiosarcoma Notch2 Oncology Tumor Biology |
author_facet |
Keisuke Aoshima Yuki Fukui Kevin Christian Montecillo Gulay Ochbayar Erdemsurakh Atsuya Morita Atsushi Kobayashi Takashi Kimura |
author_sort |
Keisuke Aoshima |
title |
Notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cells |
title_short |
Notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cells |
title_full |
Notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cells |
title_fullStr |
Notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cells |
title_full_unstemmed |
Notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cells |
title_sort |
notch2 signal is required for the maintenance of canine hemangiosarcoma cancer stem cell-like cells |
publisher |
BMC |
series |
BMC Veterinary Research |
issn |
1746-6148 |
publishDate |
2018-10-01 |
description |
Abstract Background Hemangiosarcoma (HSA) is a malignant tumor derived from endothelial cells which usually shows poor prognosis due to its high invasiveness, metastatic rate and severe hemorrhage from tumor ruptures. Since the pathogenesis of HSA is not yet complete, further understanding of its molecular basis is required. Results Here, we identified Notch2 signal as a key factor in maintaining canine HSA cancer stem cell (CSC)-like cells. We first cultured HSA cell lines in adherent serum-free condition and confirmed their CSC-like characteristics. Notch signal was upregulated in the CSC-like cells and Notch signal inhibition by a γ-secretase inhibitor significantly repressed their growth. Notch2, a Notch receptor, was highly expressed in the CSC-like cells. Constitutive activation of Notch2 increased clonogenicity and number of cells which were able to survive in serum-free condition. In contrast, inhibition of Notch2 activity showed opposite effects. These results suggest that Notch2 is an important factor for maintaining HSA CSC-like cells. Neoplastic cells in clinical cases also express Notch2 higher than endothelial cells in the normal blood vessels in the same slides. Conclusion This study provides foundation for further stem cell research in HSA and can provide a way to develop effective treatments to CSCs of endothelial tumors. |
topic |
Cancer stem cell-like cells Hemangiosarcoma Notch2 Oncology Tumor Biology |
url |
http://link.springer.com/article/10.1186/s12917-018-1624-8 |
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