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Identification of PTPRZ as a drug target for cancer stem cells in glioblastoma

07.18.17 | National Institutes of Natural Sciences

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Glioblastoma is the most malignant brain tumor with high mortality. Cancer stem cells are thought to be crucial for tumor initiation and its recurrence after standard therapy with radiation and temozolomide (TMZ) chemotherapy. Protein tyrosine phosphatase receptor type Z (PTPRZ) is an enzyme that is highly expressed in glioblastoma, especially in cancer stem cells.

The research group of Professor Masaharu Noda and Researcher Akihiro Fujikawa of the National Institute for Basic Biology (NIBB) showed that the enzymatic activity of PTPRZ is requisite for the maintenance of stem cell properties and tumorigenicity in glioblastoma cells. PTPRZ knockdown strongly inhibited tumor growth of C6 glioblastoma cells in a mouse xenograft model. In addition, the research team discovered NAZ2329, an allosteric inhibitor of PTPRZ, in collaboration with ASUBIO Pharma Co. Ltd.. NAZ2329 efficiently suppressed stem cell-like properties of glioblastoma cells in culture, and tumor growth in C6 glioblastoma xenografts. These results indicate that pharmacological inhibition of PTPRZ is a promising strategy for the treatment of malignant gliomas.

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The results of this research were published in Scientific Reports on June 17th, 2017.

Scientific Reports

10.1038/s41598-017-05931-8

Keywords

Article Information

Contact Information

Masaharu Noda
madon@nibb.ac.jp

Source

How to Cite This Article

APA:
National Institutes of Natural Sciences. (2017, July 18). Identification of PTPRZ as a drug target for cancer stem cells in glioblastoma. Brightsurf News. https://www.brightsurf.com/news/8JXJ97RL/identification-of-ptprz-as-a-drug-target-for-cancer-stem-cells-in-glioblastoma.html
MLA:
"Identification of PTPRZ as a drug target for cancer stem cells in glioblastoma." Brightsurf News, Jul. 18 2017, https://www.brightsurf.com/news/8JXJ97RL/identification-of-ptprz-as-a-drug-target-for-cancer-stem-cells-in-glioblastoma.html.