Cargando…
Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression
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 IC(50) of GA stimulating T24 cells for 24, 48, and 72 h were 21.73, 18.62, and 11.59 µ...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468429/ https://www.ncbi.nlm.nih.gov/pubmed/32973496 http://dx.doi.org/10.3389/fphar.2020.01222 |
_version_ | 1783578215998029824 |
---|---|
author | Zeng, Maolin Su, Yang Li, Kuangyu Jin, Dan Li, Qiaoling Li, Yan Zhou, Benhong |
author_facet | Zeng, Maolin Su, Yang Li, Kuangyu Jin, Dan Li, Qiaoling Li, Yan Zhou, Benhong |
author_sort | Zeng, Maolin |
collection | PubMed |
description | 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 IC(50) of GA stimulating T24 cells for 24, 48, and 72 h were 21.73, 18.62, and 11.59 µg/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-IκBα, P-IKKα, and P-NF-κB 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-κB p65 genes expression (p < 0.001). However, on the basis of GA (IC(50)) 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-κB signaling suppression. Our study will help in finding a safe and effective treatment for bladder cancer. |
format | Online Article Text |
id | pubmed-7468429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74684292020-09-23 Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression Zeng, Maolin Su, Yang Li, Kuangyu Jin, Dan Li, Qiaoling Li, Yan Zhou, Benhong Front Pharmacol Pharmacology 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 IC(50) of GA stimulating T24 cells for 24, 48, and 72 h were 21.73, 18.62, and 11.59 µg/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-IκBα, P-IKKα, and P-NF-κB 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-κB p65 genes expression (p < 0.001). However, on the basis of GA (IC(50)) 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-κB signaling suppression. Our study will help in finding a safe and effective treatment for bladder cancer. Frontiers Media S.A. 2020-08-20 /pmc/articles/PMC7468429/ /pubmed/32973496 http://dx.doi.org/10.3389/fphar.2020.01222 Text en Copyright © 2020 Zeng, Su, Li, Jin, Li, Li and Zhou http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Zeng, Maolin Su, Yang Li, Kuangyu Jin, Dan Li, Qiaoling Li, Yan Zhou, Benhong Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression |
title | Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression |
title_full | Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression |
title_fullStr | Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression |
title_full_unstemmed | Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression |
title_short | Gallic Acid Inhibits Bladder Cancer T24 Cell Progression Through Mitochondrial Dysfunction and PI3K/Akt/NF-κB Signaling Suppression |
title_sort | gallic acid inhibits bladder cancer t24 cell progression through mitochondrial dysfunction and pi3k/akt/nf-κb signaling suppression |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468429/ https://www.ncbi.nlm.nih.gov/pubmed/32973496 http://dx.doi.org/10.3389/fphar.2020.01222 |
work_keys_str_mv | AT zengmaolin gallicacidinhibitsbladdercancert24cellprogressionthroughmitochondrialdysfunctionandpi3kaktnfkbsignalingsuppression AT suyang gallicacidinhibitsbladdercancert24cellprogressionthroughmitochondrialdysfunctionandpi3kaktnfkbsignalingsuppression AT likuangyu gallicacidinhibitsbladdercancert24cellprogressionthroughmitochondrialdysfunctionandpi3kaktnfkbsignalingsuppression AT jindan gallicacidinhibitsbladdercancert24cellprogressionthroughmitochondrialdysfunctionandpi3kaktnfkbsignalingsuppression AT liqiaoling gallicacidinhibitsbladdercancert24cellprogressionthroughmitochondrialdysfunctionandpi3kaktnfkbsignalingsuppression AT liyan gallicacidinhibitsbladdercancert24cellprogressionthroughmitochondrialdysfunctionandpi3kaktnfkbsignalingsuppression AT zhoubenhong gallicacidinhibitsbladdercancert24cellprogressionthroughmitochondrialdysfunctionandpi3kaktnfkbsignalingsuppression |