STAT3 phosphorylation inhibitor Bt354 exhibits anti-neoplastic activity in glioblastoma multiforme cells.
Yi-Chun ChiangPadhmavathi SelvamYou-Xuan LiuPo-Chang ShihNan-Fu ChenHsiao-Mei KuoHugo You-Hsien LinZhi-Hong WenWu-Fu ChenPublished in: Environmental toxicology (2024)
The high mortality rate of glioblastoma multiforme (GBM), a lethal primary brain tumor, is attributable to postsurgical recurrence. STAT3, an oncogenic protein, is a signal transducer and transcription activator encourages cancer cell migration and proliferation, which results in resistance to therapy. STAT3 inhibition reduces cancer metastasis and improves patient prognosis. Bt354, a small molecule STAT inhibitor, exhibits significant cytotoxic and anti-proliferative activities against certain cancer types. Here, we demonstrated that exposure of GBM cells (U87 MG) to Bt354 had a significant, concentration-dependent growth suppression. Bt354 also induced apoptosis and downregulated the expression of the epithelial-mesenchymal transition genes. Therefore, this study suggests the potential of Bt354 for treating GBM owing to its ability to induce cytotoxicity.
Keyphrases
- induced apoptosis
- signaling pathway
- endoplasmic reticulum stress
- papillary thyroid
- epithelial mesenchymal transition
- small molecule
- oxidative stress
- cell migration
- cell proliferation
- squamous cell
- poor prognosis
- transcription factor
- type diabetes
- gene expression
- lymph node metastasis
- childhood cancer
- long non coding rna
- immune response
- risk factors
- climate change
- young adults
- pi k akt
- human health
- replacement therapy