Cargando…
Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture
Gecko (Gekko japonicus) extracts have been used in traditional Chinese medicine for many years. It has been proven that the gecko polypeptide mixture (GPM) extracted from gecko can inhibit the growth of multiple types of tumor cells. In order to investigate the possible anti-tumor molecular mechanis...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072819/ https://www.ncbi.nlm.nih.gov/pubmed/30087713 http://dx.doi.org/10.7150/jca.26339 |
_version_ | 1783344064415924224 |
---|---|
author | Duan, Yi-Meng Jin, Ying Guo, Meng-Li Duan, Leng-Xin Wang, Jian-Gang |
author_facet | Duan, Yi-Meng Jin, Ying Guo, Meng-Li Duan, Leng-Xin Wang, Jian-Gang |
author_sort | Duan, Yi-Meng |
collection | PubMed |
description | Gecko (Gekko japonicus) extracts have been used in traditional Chinese medicine for many years. It has been proven that the gecko polypeptide mixture (GPM) extracted from gecko can inhibit the growth of multiple types of tumor cells. In order to investigate the possible anti-tumor molecular mechanisms of GPM, we used RNA-seq technology to identify the differentially expressed genes (DEGs) of human hepatocellular carcinoma (HCC) HepG2 cells treated with or without GPM. MTT assay was used to detect the viability of HepG2 cells. DAPI fluorescence staining was performed to observe morphological changes in the nuclei of HepG2 cells. Western blot analysis was applied to observe the expressions of apoptosis-related and endoplasmic reticulum stress (ERS)-related proteins in HepG2 cells. Flow cytometry assay was performed to detect the apoptosis and reactive oxygen species (ROS) in HepG2 cells. Our results showed that GPM inhibited HepG2 cells proliferation and induced the apoptosis of HepG2 cells. RNA-seq analysis suggested that the ER-nucleus signaling pathway involved in the anti-cancer molecular mechanism of GPM. Therefore, GPM may induce apoptosis in HepG2 cells via the ERs pathway. |
format | Online Article Text |
id | pubmed-6072819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-60728192018-08-07 Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture Duan, Yi-Meng Jin, Ying Guo, Meng-Li Duan, Leng-Xin Wang, Jian-Gang J Cancer Research Paper Gecko (Gekko japonicus) extracts have been used in traditional Chinese medicine for many years. It has been proven that the gecko polypeptide mixture (GPM) extracted from gecko can inhibit the growth of multiple types of tumor cells. In order to investigate the possible anti-tumor molecular mechanisms of GPM, we used RNA-seq technology to identify the differentially expressed genes (DEGs) of human hepatocellular carcinoma (HCC) HepG2 cells treated with or without GPM. MTT assay was used to detect the viability of HepG2 cells. DAPI fluorescence staining was performed to observe morphological changes in the nuclei of HepG2 cells. Western blot analysis was applied to observe the expressions of apoptosis-related and endoplasmic reticulum stress (ERS)-related proteins in HepG2 cells. Flow cytometry assay was performed to detect the apoptosis and reactive oxygen species (ROS) in HepG2 cells. Our results showed that GPM inhibited HepG2 cells proliferation and induced the apoptosis of HepG2 cells. RNA-seq analysis suggested that the ER-nucleus signaling pathway involved in the anti-cancer molecular mechanism of GPM. Therefore, GPM may induce apoptosis in HepG2 cells via the ERs pathway. Ivyspring International Publisher 2018-06-23 /pmc/articles/PMC6072819/ /pubmed/30087713 http://dx.doi.org/10.7150/jca.26339 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Duan, Yi-Meng Jin, Ying Guo, Meng-Li Duan, Leng-Xin Wang, Jian-Gang Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture |
title | Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture |
title_full | Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture |
title_fullStr | Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture |
title_full_unstemmed | Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture |
title_short | Differentially expressed genes of HepG2 cells treated with gecko polypeptide mixture |
title_sort | differentially expressed genes of hepg2 cells treated with gecko polypeptide mixture |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072819/ https://www.ncbi.nlm.nih.gov/pubmed/30087713 http://dx.doi.org/10.7150/jca.26339 |
work_keys_str_mv | AT duanyimeng differentiallyexpressedgenesofhepg2cellstreatedwithgeckopolypeptidemixture AT jinying differentiallyexpressedgenesofhepg2cellstreatedwithgeckopolypeptidemixture AT guomengli differentiallyexpressedgenesofhepg2cellstreatedwithgeckopolypeptidemixture AT duanlengxin differentiallyexpressedgenesofhepg2cellstreatedwithgeckopolypeptidemixture AT wangjiangang differentiallyexpressedgenesofhepg2cellstreatedwithgeckopolypeptidemixture |