Cargando…
Rhein Induces Oral Cancer Cell Apoptosis and ROS via Suppresse AKT/mTOR Signaling Pathway In Vitro and In Vivo
Oral cancer remains the leading cause of death worldwide. Rhein is a natural compound extracted from the traditional Chinese herbal medicine rhubarb, which has demonstrated therapeutic effects in various cancers. However, the specific effects of rhein on oral cancer are still unclear. This study aim...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218067/ https://www.ncbi.nlm.nih.gov/pubmed/37239855 http://dx.doi.org/10.3390/ijms24108507 |
_version_ | 1785048685502005248 |
---|---|
author | Zhang, Haibo Ma, Lei Kim, Eungyung Yi, Junkoo Huang, Hai Kim, Hyeonjin Raza, Muhammad Atif Park, Sijun Jang, Soyoung Kim, Kirim Kim, Sung-Hyun Lee, Youngkyun Kim, Eunkyong Ryoo, Zae Young Kim, Myoung Ok |
author_facet | Zhang, Haibo Ma, Lei Kim, Eungyung Yi, Junkoo Huang, Hai Kim, Hyeonjin Raza, Muhammad Atif Park, Sijun Jang, Soyoung Kim, Kirim Kim, Sung-Hyun Lee, Youngkyun Kim, Eunkyong Ryoo, Zae Young Kim, Myoung Ok |
author_sort | Zhang, Haibo |
collection | PubMed |
description | Oral cancer remains the leading cause of death worldwide. Rhein is a natural compound extracted from the traditional Chinese herbal medicine rhubarb, which has demonstrated therapeutic effects in various cancers. However, the specific effects of rhein on oral cancer are still unclear. This study aimed to investigate the potential anticancer activity and underlying mechanisms of rhein in oral cancer cells. The antigrowth effect of rhein in oral cancer cells was estimated by cell proliferation, soft agar colony formation, migration, and invasion assay. The cell cycle and apoptosis were detected by flow cytometry. The underlying mechanism of rhein in oral cancer cells was explored by immunoblotting. The in vivo anticancer effect was evaluated by oral cancer xenografts. Rhein significantly inhibited oral cancer cell growth by inducing apoptosis and S-phase cell cycle arrest. Rhein inhibited oral cancer cell migration and invasion through the regulation of epithelial–mesenchymal transition-related proteins. Rhein induced reactive oxygen species (ROS) accumulation in oral cancer cells to inhibit the AKT/mTOR signaling pathway. Rhein exerted anticancer activity in vitro and in vivo by inducing oral cancer cell apoptosis and ROS via the AKT/mTOR signaling pathway in oral cancer. Rhein is a potential therapeutic drug for oral cancer treatment. |
format | Online Article Text |
id | pubmed-10218067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102180672023-05-27 Rhein Induces Oral Cancer Cell Apoptosis and ROS via Suppresse AKT/mTOR Signaling Pathway In Vitro and In Vivo Zhang, Haibo Ma, Lei Kim, Eungyung Yi, Junkoo Huang, Hai Kim, Hyeonjin Raza, Muhammad Atif Park, Sijun Jang, Soyoung Kim, Kirim Kim, Sung-Hyun Lee, Youngkyun Kim, Eunkyong Ryoo, Zae Young Kim, Myoung Ok Int J Mol Sci Article Oral cancer remains the leading cause of death worldwide. Rhein is a natural compound extracted from the traditional Chinese herbal medicine rhubarb, which has demonstrated therapeutic effects in various cancers. However, the specific effects of rhein on oral cancer are still unclear. This study aimed to investigate the potential anticancer activity and underlying mechanisms of rhein in oral cancer cells. The antigrowth effect of rhein in oral cancer cells was estimated by cell proliferation, soft agar colony formation, migration, and invasion assay. The cell cycle and apoptosis were detected by flow cytometry. The underlying mechanism of rhein in oral cancer cells was explored by immunoblotting. The in vivo anticancer effect was evaluated by oral cancer xenografts. Rhein significantly inhibited oral cancer cell growth by inducing apoptosis and S-phase cell cycle arrest. Rhein inhibited oral cancer cell migration and invasion through the regulation of epithelial–mesenchymal transition-related proteins. Rhein induced reactive oxygen species (ROS) accumulation in oral cancer cells to inhibit the AKT/mTOR signaling pathway. Rhein exerted anticancer activity in vitro and in vivo by inducing oral cancer cell apoptosis and ROS via the AKT/mTOR signaling pathway in oral cancer. Rhein is a potential therapeutic drug for oral cancer treatment. MDPI 2023-05-09 /pmc/articles/PMC10218067/ /pubmed/37239855 http://dx.doi.org/10.3390/ijms24108507 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Haibo Ma, Lei Kim, Eungyung Yi, Junkoo Huang, Hai Kim, Hyeonjin Raza, Muhammad Atif Park, Sijun Jang, Soyoung Kim, Kirim Kim, Sung-Hyun Lee, Youngkyun Kim, Eunkyong Ryoo, Zae Young Kim, Myoung Ok Rhein Induces Oral Cancer Cell Apoptosis and ROS via Suppresse AKT/mTOR Signaling Pathway In Vitro and In Vivo |
title | Rhein Induces Oral Cancer Cell Apoptosis and ROS via Suppresse AKT/mTOR Signaling Pathway In Vitro and In Vivo |
title_full | Rhein Induces Oral Cancer Cell Apoptosis and ROS via Suppresse AKT/mTOR Signaling Pathway In Vitro and In Vivo |
title_fullStr | Rhein Induces Oral Cancer Cell Apoptosis and ROS via Suppresse AKT/mTOR Signaling Pathway In Vitro and In Vivo |
title_full_unstemmed | Rhein Induces Oral Cancer Cell Apoptosis and ROS via Suppresse AKT/mTOR Signaling Pathway In Vitro and In Vivo |
title_short | Rhein Induces Oral Cancer Cell Apoptosis and ROS via Suppresse AKT/mTOR Signaling Pathway In Vitro and In Vivo |
title_sort | rhein induces oral cancer cell apoptosis and ros via suppresse akt/mtor signaling pathway in vitro and in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218067/ https://www.ncbi.nlm.nih.gov/pubmed/37239855 http://dx.doi.org/10.3390/ijms24108507 |
work_keys_str_mv | AT zhanghaibo rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT malei rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT kimeungyung rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT yijunkoo rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT huanghai rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT kimhyeonjin rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT razamuhammadatif rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT parksijun rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT jangsoyoung rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT kimkirim rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT kimsunghyun rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT leeyoungkyun rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT kimeunkyong rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT ryoozaeyoung rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo AT kimmyoungok rheininducesoralcancercellapoptosisandrosviasuppresseaktmtorsignalingpathwayinvitroandinvivo |