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Gli1 regulates stemness characteristics in gastric adenocarcinoma
BACKGROUND: Glioma-associated oncogene homolog 1 (Gli1), affects the progression and the stemness characteristics of malignant carcinoma. The aim of the present study was to identify the relation between Glioma-associated oncogene homolog 1 (Gli1) and stemness and determine its clinical significance...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236965/ https://www.ncbi.nlm.nih.gov/pubmed/32430068 http://dx.doi.org/10.1186/s13000-020-00949-5 |
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author | Qi, Wenbo Yang, Zhaoting Feng, Ying Li, Haoyue Che, Nan Liu, Lan Xuan, Yanhua |
author_facet | Qi, Wenbo Yang, Zhaoting Feng, Ying Li, Haoyue Che, Nan Liu, Lan Xuan, Yanhua |
author_sort | Qi, Wenbo |
collection | PubMed |
description | BACKGROUND: Glioma-associated oncogene homolog 1 (Gli1), affects the progression and the stemness characteristics of malignant carcinoma. The aim of the present study was to identify the relation between Glioma-associated oncogene homolog 1 (Gli1) and stemness and determine its clinical significance in gastric adenocarcinoma (GA). We investigated Gli1 expression and its correlation with other stemness-associated proteins in 169 GA samples and 5 GA cell lines. METHODS: To elucidate the role of Gli1 in the clinicopathological significance and stemness of GA, tissues samples from 169 GA patients were collected for immunohistochemistry (IHC). Additionally, MKN74, MKN28, NCI-N87, SNU638, AGS cells were collected for western blotting, MKN28 cells were collected for spheroid formation assay. RESULTS: Results showed that Gli1 expression was closely related to tumor grade, primary tumor (pT) stage, distant metastasis, clinical stage, gross type, microvessel density, and shorter overall survival (OS). Cox regression analysis verified that Gli1 was an independent prognostic factor for OS. Furthermore, Gli1 expression correlated with the expression of stemness-related genes, CD44, LSD1, and Sox9. Gli1 inhibitor GANT61 significantly decreased the expression of CD44 and LSD1, and spheroid formation ability of the MKN28 cells. CONCLUSIONS: In conclusion, Gli1 may be a poor prognostic indicator and a potential cancer stemness-related protein in GA. |
format | Online Article Text |
id | pubmed-7236965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72369652020-05-27 Gli1 regulates stemness characteristics in gastric adenocarcinoma Qi, Wenbo Yang, Zhaoting Feng, Ying Li, Haoyue Che, Nan Liu, Lan Xuan, Yanhua Diagn Pathol Research BACKGROUND: Glioma-associated oncogene homolog 1 (Gli1), affects the progression and the stemness characteristics of malignant carcinoma. The aim of the present study was to identify the relation between Glioma-associated oncogene homolog 1 (Gli1) and stemness and determine its clinical significance in gastric adenocarcinoma (GA). We investigated Gli1 expression and its correlation with other stemness-associated proteins in 169 GA samples and 5 GA cell lines. METHODS: To elucidate the role of Gli1 in the clinicopathological significance and stemness of GA, tissues samples from 169 GA patients were collected for immunohistochemistry (IHC). Additionally, MKN74, MKN28, NCI-N87, SNU638, AGS cells were collected for western blotting, MKN28 cells were collected for spheroid formation assay. RESULTS: Results showed that Gli1 expression was closely related to tumor grade, primary tumor (pT) stage, distant metastasis, clinical stage, gross type, microvessel density, and shorter overall survival (OS). Cox regression analysis verified that Gli1 was an independent prognostic factor for OS. Furthermore, Gli1 expression correlated with the expression of stemness-related genes, CD44, LSD1, and Sox9. Gli1 inhibitor GANT61 significantly decreased the expression of CD44 and LSD1, and spheroid formation ability of the MKN28 cells. CONCLUSIONS: In conclusion, Gli1 may be a poor prognostic indicator and a potential cancer stemness-related protein in GA. BioMed Central 2020-05-19 /pmc/articles/PMC7236965/ /pubmed/32430068 http://dx.doi.org/10.1186/s13000-020-00949-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Qi, Wenbo Yang, Zhaoting Feng, Ying Li, Haoyue Che, Nan Liu, Lan Xuan, Yanhua Gli1 regulates stemness characteristics in gastric adenocarcinoma |
title | Gli1 regulates stemness characteristics in gastric adenocarcinoma |
title_full | Gli1 regulates stemness characteristics in gastric adenocarcinoma |
title_fullStr | Gli1 regulates stemness characteristics in gastric adenocarcinoma |
title_full_unstemmed | Gli1 regulates stemness characteristics in gastric adenocarcinoma |
title_short | Gli1 regulates stemness characteristics in gastric adenocarcinoma |
title_sort | gli1 regulates stemness characteristics in gastric adenocarcinoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236965/ https://www.ncbi.nlm.nih.gov/pubmed/32430068 http://dx.doi.org/10.1186/s13000-020-00949-5 |
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