PTPRM methylation induced by FN1 promotes the development of glioblastoma by activating STAT3 signalling

The phosphorylation of signal transducer and activator of transcription protein 3 (STAT3) is up-regulated in glioblastoma (GBM) cells and is regulated by protein tyrosine phosphatase receptor type M (PTPRM). Fibronectin-1 (FN1) is also reported to be up-regulated in GBM. We explored the role of FN1-...

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Veröffentlicht in:Pharmaceutical biology 2021-01, Vol.59 (1), p.902-909
Hauptverfasser: Song, Jian, Zhao, Di, Sun, Guozhu, Yang, Jiankai, Lv, Zhongqiang, Jiao, Baohua
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Sprache:eng
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Zusammenfassung:The phosphorylation of signal transducer and activator of transcription protein 3 (STAT3) is up-regulated in glioblastoma (GBM) cells and is regulated by protein tyrosine phosphatase receptor type M (PTPRM). Fibronectin-1 (FN1) is also reported to be up-regulated in GBM. We explored the role of FN1-induced PTPRM methylation in GBM. The lentivirus particles of oe-PTPRM, sh-PTPRM, oe-FN1, sh-FN1, or their negative controls (NSCs) were transfected into GBM cells with or without stattic (0.5 μM, 24 h) or 5-aza (1 μM, 0, 2, 4 h) treatments. Methylation-specific PCR was performed to detect PTPRM methylation levels. PTPRM was down-regulated (0.373 ± 0.124- and 0.455 ± 0.109-fold), FN1 and p-STAT3 were up-regulated (p 
ISSN:1388-0209
1744-5116
DOI:10.1080/13880209.2021.1944220