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MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis

  • Authors:
    • Mizuho Ishikawa
    • Mitsuhiko Osaki
    • Narumi Uno
    • Takahito Ohira
    • Hiroyuki Kugoh
    • Futoshi Okada
  • View Affiliations / Copyright

    Affiliations: Division of Experimental Pathology, Faculty of Medicine, Tottori University, Yonago, Tottori 683‑8503, Japan, Chromosome Engineering Research Center, Faculty of Medicine, Tottori University, Yonago, Tottori 683‑8503, Japan
    Copyright: © Ishikawa et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 11
    |
    Published online on: November 9, 2021
       https://doi.org/10.3892/mmr.2021.12527
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Abstract

Our previous study revealed that metastasis‑associated protein 1 (MTA1), which is expressed in vascular endothelial cells, acts as a tube formation promoting factor. The present study aimed to clarify the importance of MTA1 expression in tube formation using MTA1‑knockout (KO) endothelial cells (MTA1‑KO MSS31 cells). Tube formation was significantly suppressed in MTA1‑KO MSS31 cells, whereas MTA1‑overexpression MTA1‑KO MSS31 cells regained the ability to form tube‑like structures. In addition, western blotting analysis revealed that MTA1‑KO MSS31 cells showed significantly higher levels of phosphorylation of non‑muscle myosin heavy chain IIa, which resulted in suppression of tube formation. This effect was attributed to a decrease of MTA1/S100 calcium‑binding protein A4 complex formation. Moreover, inhibition of tube formation in MTA1‑KO MSS31 cells could not be rescued by stimulation with vascular endothelial growth factor (VEGF). These results demonstrated that MTA1 may serve as an essential molecule for angiogenesis in endothelial cells and be involved in different steps of the angiogenic process compared with the VEGF/VEGF receptor 2 pathway. The findings showed that endothelial MTA1 and its pathway may serve as promising targets for inhibiting tumor angiogenesis, further supporting the development of MTA1‑based antiangiogenic therapies.
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Copy and paste a formatted citation
Spandidos Publications style
Ishikawa M, Osaki M, Uno N, Ohira T, Kugoh H and Okada F: MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis. Mol Med Rep 25: 11, 2022.
APA
Ishikawa, M., Osaki, M., Uno, N., Ohira, T., Kugoh, H., & Okada, F. (2022). MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis. Molecular Medicine Reports, 25, 11. https://doi.org/10.3892/mmr.2021.12527
MLA
Ishikawa, M., Osaki, M., Uno, N., Ohira, T., Kugoh, H., Okada, F."MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis". Molecular Medicine Reports 25.1 (2022): 11.
Chicago
Ishikawa, M., Osaki, M., Uno, N., Ohira, T., Kugoh, H., Okada, F."MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis". Molecular Medicine Reports 25, no. 1 (2022): 11. https://doi.org/10.3892/mmr.2021.12527
Copy and paste a formatted citation
x
Spandidos Publications style
Ishikawa M, Osaki M, Uno N, Ohira T, Kugoh H and Okada F: MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis. Mol Med Rep 25: 11, 2022.
APA
Ishikawa, M., Osaki, M., Uno, N., Ohira, T., Kugoh, H., & Okada, F. (2022). MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis. Molecular Medicine Reports, 25, 11. https://doi.org/10.3892/mmr.2021.12527
MLA
Ishikawa, M., Osaki, M., Uno, N., Ohira, T., Kugoh, H., Okada, F."MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis". Molecular Medicine Reports 25.1 (2022): 11.
Chicago
Ishikawa, M., Osaki, M., Uno, N., Ohira, T., Kugoh, H., Okada, F."MTA1, a metastasis‑associated protein, in endothelial cells is an essential molecule for angiogenesis". Molecular Medicine Reports 25, no. 1 (2022): 11. https://doi.org/10.3892/mmr.2021.12527
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