Apigenin and Temozolomide Synergistically Inhibit Glioma Growth Through the PI3K / AKT Pathway

• Published in: Cancer biotherapy & radiopharmaceuticals Vol. 39; no. 2; p. 125
• Main Authors: Wang, Dong, Wang, Zhijun, Dai, Xuedong, Zhang, Liang, Li, Min
• Format: Journal Article
• Language: English
• Published: United States 01.03.2024
• Subjects: Animals; Apigenin - pharmacology; Apigenin - therapeutic use; Apoptosis; Brain Neoplasms - genetics; Cell Line, Tumor; Cell Proliferation; Glioma - genetics; Humans; Metalloproteases - pharmacology; Mice; Phosphatidylinositol 3-Kinases - metabolism; Proto-Oncogene Proteins c-akt - metabolism; Temozolomide - pharmacology; Temozolomide - therapeutic use; temozolomide; apigenin; glioma; AKT; proliferation
• ISSN: 1557-8852
• DOI: 10.1089/cbr.2020.4283

Glioma is a devastating disease with the worst prognosis among human malignant tumors. Although temozolomide (TMZ) improves the overall survival of glioma patients, there are still many glioma patients who are resistant to TMZ. In this study, we focused on the effect of apigenin (API) and TMZ on glioma cells and , and we studied the underlying molecular mechanisms. To investigate the effect of API on glioblastoma cell proliferation, cell viability was assessed after glioma cells were incubated with various concentrations of API with or without TMZ using MTT assays. Then, we explored the synergistic effect of API and TMZ on glioma cell cycle, apoptosis, and migration. To investigate the molecular mechanism behind the synergism of API and TMZ, we examined the related genes of the major signaling pathways involved in glioma pathogenesis by Western blotting. In this study, we found that API significantly suppressed the proliferation of glioma cells in a dose- and time-dependent manner. Combining API and TMZ significantly induced glioma cells arrest at the G2 phase and inhibited glioma cells proliferation compared with API or TMZ alone. In addition, API promoted the ability of TMZ to induce glioma cells apoptosis and inhibit glioma cells invasion. Furthermore, compared with treatment with individual agents, the combination of API and TMZ significantly inhibited the growth of subcutaneous tumors in mice. These results implied that API could synergistically suppress the growth of glioma cells when combined with TMZ. Combining API and TMZ significantly inhibited the protein expression of , , Bcl-2, Matrix Metallopeptidase 2, and Matrix Metallopeptidase 9. API and TMZ synergistically inhibited glioma growth through the / pathway.