Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression

被引:42
作者
Zeng, Maolin [1 ,2 ]
Su, Yang [3 ,4 ,5 ]
Li, Kuangyu [6 ,7 ]
Jin, Dan [1 ]
Li, Qiaoling [6 ]
Li, Yan [1 ]
Zhou, Benhong [1 ,6 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Pharm, Wuhan, Peoples R China
[2] Chongqing Med Univ, Yongchuan Hosp, Dept Pharm, Yongchuan, Peoples R China
[3] Anhui Med Univ, Affiliated Hosp 1, Dept Urol, Hefei, Peoples R China
[4] Anhui Med Univ, Anhui Prov Key Lab Genitourinary Dis, Hefei, Peoples R China
[5] Anhui Med Univ, Inst Urol, Hefei, Peoples R China
[6] Wuhan Univ, Sch Pharmaceut Sci, Wuhan, Peoples R China
[7] Jianghan Univ, Hubei Peoples Hosp 3, Dept Pharm, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
gallic acid; bladder cancer; proliferation; metastasis; apoptosis; GROWTH-FACTOR VEGF; APOPTOSIS; PATHWAY; CISPLATIN; PI3K/AKT; P53;
D O I
10.3389/fphar.2020.01222
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gallic acid (GA), a hydrolyzable tannin, has a wide range of pharmacological activities. This study revealed that, GA significantly inhibited T24 cells viability in a concentration- and time- dependent manner. The IC50 of GA stimulating T24 cells for 24, 48, and 72 h were 21.73, 18.62, and 11.59 mu g/ml respectively, and the inhibition rate was significantly higher than the positive control drug selected for CCK-8 assay. Meanwhile, after GA treatment, the morphology of T24 cells were changed significantly. Moreover, GA significantly inhibited T24 cells proliferation and blocked T24 cells cycle in S phase (p < 0.001). GA induced T24 cells apoptosis (p < 0.001), accompanied by reactive oxygen species (ROS) accumulation and mitochondrial membrane potential (MMP) depolarization. Western blotting analysis showed that GA significantly increased Cleaved caspase-3, Bax, P53, and Cytochrome C (Cyt-c) proteins expression, and decreased Bcl-2, P-PI3K, P-Akt, P-I kappa B alpha, P-IKK alpha, and P-NF-kappa B p65 proteins expression in T24 cells (p < 0.05). Real-Time PCR results verified that GA significantly promoted Caspase-3, Bax, P53, and Cyt-c genes expression, and inhibited Bcl-2, PI3K, Akt, and NF-kappa B p65 genes expression (p < 0.001). However, on the basis of GA (IC50) stimulation, NAC (an oxidative stress inhibitor) pretreatment reversed the apoptotic rate of T24 cells and the expression of Bax, Cleaved caspase-3, P53, Bcl-2 proteins, and the MMP level in T24 cells, as well as the expression of Cyt-c protein in T24 cells mitochondria and cytoplasm. In addition, GA significantly suppressed T24 cells migration and invasion ability with VEGF protein inhibition (p < 0.001). Briefly, GA can inhibit T24 cells proliferation, metastasis and promote apoptosis, and the pro-apoptotic activity is closely associated with mitochondrial dysfunction and PI3K/Akt/NF-kappa B signaling suppression. Our study will help in finding a safe and effective treatment for bladder cancer.
引用
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页数:17
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