TCAF2 drives glioma cellular migratory/invasion properties through STAT3 signaling

Glioma is an intracranial tumor characterized by high mortality and recurrence rates. In the present study, the association of TRPM8 channel-associated factor 2 (TCAF2) in glioma was investigated using bioinformatics, showing significant relationships with age, WHO grade, IDH, and 1p/19q status, as well as being an independent predictor of prognosis. Immunohistochemistry of a glioma sample microarray showed markedly increased TCAF2 expression in glioblastoma relative to lower-grade glioma, with elevated expression predominating in the tumor center. Raised TCAF2 levels promote glioma cell migratory/invasion properties through the epithelial-to-mesenchymal transition-like (EMT-like) process, shown by Transwell and scratch assays and western blotting. It was further found that the effects of TCAF2 were mediated by the activation of STAT3. These results suggest that TCAF2 promotes glioma cell migration and invasion, rendering it a potential drug target in glioma therapy.

Automated summary

This study investigated the association of TRPM8 channel-associated factor 2 (TCAF2) in glioma and found significant relationships with age, WHO grade, IDH, and 1p/19q status. TCAF2 expression was markedly increased in glioblastoma compared to lower-grade glioma and promoted glioma cell migration and invasion through the activation of STAT3.