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Knockdown of DSPP inhibits the migration and invasion of glioma cells. | LitMetric

Knockdown of DSPP inhibits the migration and invasion of glioma cells.

Pathol Res Pract

Department of Neurosurgery, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, China. Electronic address:

Published: December 2018

AI Article Synopsis

  • Dentin sialophosphoprotein (DSPP) is part of the SIBLING family and is linked to the movement of solid tumor cells, but its role in glioma is not well understood.
  • This study found that DSPP is overexpressed in glioma tissues compared to normal brain tissues and that reducing DSPP levels with siRNA significantly decreased glioma cell migration and invasion.
  • Additionally, the down-regulation of DSPP was shown to inhibit the activation of the AKT/mTOR/p70S6K signaling pathway, suggesting that targeting DSPP could be a promising approach for glioma treatment.

Article Abstract

Dentin sialophosphoprotein (DSPP) is a member of the SIBLING (Small integrin-binding ligand N-linked glycoproteins) family of phosphoglycoproteins and has been proved to contribute to the migration of a variety of solid tumor cells. However, whether DSPP participates in the pathogenic process of glioma remains unknown. In this study, we aimed to investigate the expression and biological function of DSPP in human glioma cells. We demonstrated through Western blot that DSPP is overexpressed in glioma tissues comparing to normal brain tissues. To investigate the role of DSPP in glioma carcinogenesis, we reduced the DSPP expression by small interfering RNA (siRNA) and found that DSPP silencing significantly inhibited the migration and invasion of glioma cells, the critical characteristics of glioma. Furthermore, we showed that DSPP down-regulation significantly decreased the activation of the AKT/mTOR/p70S6K pathway in glioma cells. Taken together, these findings indicate that knockdown of DSPP inhibits glioma cells migration and invasion, suggesting that targeting DSPP might be a potentially effective therapeutic strategy for treating glioma.

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Source
http://dx.doi.org/10.1016/j.prp.2018.09.024DOI Listing

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