Wang Dong, Wang Zhijun, Dai Xuedong, Zhang Liang, Li Min
Department of Neurosurgery, The Affiliated Jiangning Hospital with Nanjing Medical University, Nanjing, People's Republic of China.
Clinical Medicine, Weifang Medical University, Weifang, People's Republic of China.
Cancer Biother Radiopharm. 2024 Mar;39(2):125-132. doi: 10.1089/cbr.2020.4283. Epub 2021 Jan 20.
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.
神经胶质瘤是一种毁灭性疾病,在人类恶性肿瘤中预后最差。尽管替莫唑胺(TMZ)可提高神经胶质瘤患者的总生存率,但仍有许多神经胶质瘤患者对TMZ耐药。在本研究中,我们聚焦于芹菜素(API)和TMZ对神经胶质瘤细胞的作用,并研究其潜在的分子机制。为了研究API对胶质母细胞瘤细胞增殖的影响,使用MTT法在神经胶质瘤细胞与不同浓度的API(有无TMZ)孵育后评估细胞活力。然后,我们探究了API和TMZ对神经胶质瘤细胞周期、凋亡和迁移的协同作用。为了研究API和TMZ协同作用背后的分子机制,我们通过蛋白质印迹法检测了神经胶质瘤发病机制中主要信号通路的相关基因。在本研究中,我们发现API以剂量和时间依赖性方式显著抑制神经胶质瘤细胞的增殖。与单独使用API或TMZ相比,联合使用API和TMZ显著诱导神经胶质瘤细胞停滞在G2期并抑制神经胶质瘤细胞增殖。此外,API增强了TMZ诱导神经胶质瘤细胞凋亡和抑制神经胶质瘤细胞侵袭的能力。此外,与单独使用药物治疗相比,API和TMZ联合使用显著抑制了小鼠皮下肿瘤的生长。这些结果表明,API与TMZ联合使用时可协同抑制神经胶质瘤细胞的生长。联合使用API和TMZ显著抑制了 、 、Bcl-2、基质金属蛋白酶2和基质金属蛋白酶9的蛋白表达。API和TMZ通过 / 途径协同抑制神经胶质瘤生长。