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Anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo

PURPOSE: : Carrimycin is a newly synthesized macrolide antibiotic with good antibacterial effect. Exploratory experiments found its function in regulating cell physiology, proliferation and immunity, suggesting its potential anti-tumor capacity. The aim of this study is to investigate the anti-tumor...

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Autores principales: Liang, Si-yuan, Zhao, Tong-chao, Zhou, Zhi-hang, Ju, Wu-tong, Liu, Ying, Tan, Yi-ran, Zhu, Dong-wang, Zhang, Zhi-yuan, Zhong, Lai-ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985557/
https://www.ncbi.nlm.nih.gov/pubmed/33744726
http://dx.doi.org/10.1016/j.tranon.2021.101074
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author Liang, Si-yuan
Zhao, Tong-chao
Zhou, Zhi-hang
Ju, Wu-tong
Liu, Ying
Tan, Yi-ran
Zhu, Dong-wang
Zhang, Zhi-yuan
Zhong, Lai-ping
author_facet Liang, Si-yuan
Zhao, Tong-chao
Zhou, Zhi-hang
Ju, Wu-tong
Liu, Ying
Tan, Yi-ran
Zhu, Dong-wang
Zhang, Zhi-yuan
Zhong, Lai-ping
author_sort Liang, Si-yuan
collection PubMed
description PURPOSE: : Carrimycin is a newly synthesized macrolide antibiotic with good antibacterial effect. Exploratory experiments found its function in regulating cell physiology, proliferation and immunity, suggesting its potential anti-tumor capacity. The aim of this study is to investigate the anti-tumor effect of carrimycin against human oral squamous cell carcinoma cells in vitro and in vivo. METHODS: : Human oral squamous cell carcinoma cells (HN30/HN6/Cal27/HB96 cell lines) were treated with gradient concentration of carrimycin. Cell proliferation, colony formation and migration ability were analyzed. Cell cycle and apoptosis were assessed by flow cytometry. The effect of carrimycin on OSCC in vivo was investigated in tumor xenograft models. Immunohistochemistry, western blot assay and TUNEL assays of tissue samples from xenografts were performed. The key proteins in PI3K/AKT/mTOR pathway and MAPK pathway were examined by western blot. RESULTS: : As the concentration of carrimycin increased, the proliferation, colony formation and migration ability of OSCC cells were inhibited. After treating with carrimycin, cell cycle was arrested in G0/G1 phase and cell apoptosis was promoted. The tumor growth of xenografts was significantly suppressed. Furthermore, the expression of p-PI3K, p-AKT, p-mTOR, p-S6K, p-4EBP1, p-ERK and p-p38 were down-regulated in vitro and in vivo. CONCLUSIONS: : Carrimycin can inhibit the biological activities of OSCC cells in vitro and in vivo, and regulate the PI3K/AKT/mTOR and MAPK pathways.
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spelling pubmed-79855572021-04-01 Anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo Liang, Si-yuan Zhao, Tong-chao Zhou, Zhi-hang Ju, Wu-tong Liu, Ying Tan, Yi-ran Zhu, Dong-wang Zhang, Zhi-yuan Zhong, Lai-ping Transl Oncol Original Research PURPOSE: : Carrimycin is a newly synthesized macrolide antibiotic with good antibacterial effect. Exploratory experiments found its function in regulating cell physiology, proliferation and immunity, suggesting its potential anti-tumor capacity. The aim of this study is to investigate the anti-tumor effect of carrimycin against human oral squamous cell carcinoma cells in vitro and in vivo. METHODS: : Human oral squamous cell carcinoma cells (HN30/HN6/Cal27/HB96 cell lines) were treated with gradient concentration of carrimycin. Cell proliferation, colony formation and migration ability were analyzed. Cell cycle and apoptosis were assessed by flow cytometry. The effect of carrimycin on OSCC in vivo was investigated in tumor xenograft models. Immunohistochemistry, western blot assay and TUNEL assays of tissue samples from xenografts were performed. The key proteins in PI3K/AKT/mTOR pathway and MAPK pathway were examined by western blot. RESULTS: : As the concentration of carrimycin increased, the proliferation, colony formation and migration ability of OSCC cells were inhibited. After treating with carrimycin, cell cycle was arrested in G0/G1 phase and cell apoptosis was promoted. The tumor growth of xenografts was significantly suppressed. Furthermore, the expression of p-PI3K, p-AKT, p-mTOR, p-S6K, p-4EBP1, p-ERK and p-p38 were down-regulated in vitro and in vivo. CONCLUSIONS: : Carrimycin can inhibit the biological activities of OSCC cells in vitro and in vivo, and regulate the PI3K/AKT/mTOR and MAPK pathways. Neoplasia Press 2021-03-18 /pmc/articles/PMC7985557/ /pubmed/33744726 http://dx.doi.org/10.1016/j.tranon.2021.101074 Text en © 2021 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Liang, Si-yuan
Zhao, Tong-chao
Zhou, Zhi-hang
Ju, Wu-tong
Liu, Ying
Tan, Yi-ran
Zhu, Dong-wang
Zhang, Zhi-yuan
Zhong, Lai-ping
Anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo
title Anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo
title_full Anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo
title_fullStr Anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo
title_full_unstemmed Anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo
title_short Anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo
title_sort anti-tumor effect of carrimycin on oral squamous cell carcinoma cells in vitro and in vivo
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985557/
https://www.ncbi.nlm.nih.gov/pubmed/33744726
http://dx.doi.org/10.1016/j.tranon.2021.101074
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