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Validating the role of PTGIS gene in colorectal cancer by bioinformatics analysis and in vitro experiments

Prostaglandin I2 synthase (PTGIS) is a member of the cytochrome P450 family. Studies have revealed that differential expression of the PTGIS gene is closely related to the pathological and physiological processes of many diseases, including breast cancer, oral squamous cell carcinoma, and head and n...

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Autores principales: Ding, Hui, Wang, Kai-yun, Chen, Si-yang, Guo, Kai-Wen, Qiu, Wen-hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543560/
https://www.ncbi.nlm.nih.gov/pubmed/37779109
http://dx.doi.org/10.1038/s41598-023-43289-2
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author Ding, Hui
Wang, Kai-yun
Chen, Si-yang
Guo, Kai-Wen
Qiu, Wen-hong
author_facet Ding, Hui
Wang, Kai-yun
Chen, Si-yang
Guo, Kai-Wen
Qiu, Wen-hong
author_sort Ding, Hui
collection PubMed
description Prostaglandin I2 synthase (PTGIS) is a member of the cytochrome P450 family. Studies have revealed that differential expression of the PTGIS gene is closely related to the pathological and physiological processes of many diseases, including breast cancer, oral squamous cell carcinoma, and head and neck cancer. However, the mechanism of action of the PTGIS gene in colorectal cancer is not fully understood. This study explored the role of PTGIS in colorectal cancer through comprehensive bioinformatics analysis and in vitro experiments, and found that the expression of PTGIS gene in colorectal cancer tissue was significantly lower than that in normal colorectal tissue (P < 0.05), and high expression of PTGIS gene was associated with poor prognosis in patients (P < 0.05). The KEGG results showed that PTGIS-related genes were mainly enriched in metabolic pathways, arachidonic acid metabolism, steroid biosynthesis, and cancer pathways. The expression of PTGIS may be related to immune infiltration. Cell experiments showed that PTGIS was expressed at a lower level in cancer. Overexpression of PTGIS inhibited apoptosis and promoted proliferation, invasion, and migration ability of SW480 colorectal cancer cells. Analysis of the PTGIS gene in this study provides a theoretical basis for further exploring the pathogenesis of colorectal cancer and finding more accurate new targets for early screening and treatment of the cancer.
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spelling pubmed-105435602023-10-03 Validating the role of PTGIS gene in colorectal cancer by bioinformatics analysis and in vitro experiments Ding, Hui Wang, Kai-yun Chen, Si-yang Guo, Kai-Wen Qiu, Wen-hong Sci Rep Article Prostaglandin I2 synthase (PTGIS) is a member of the cytochrome P450 family. Studies have revealed that differential expression of the PTGIS gene is closely related to the pathological and physiological processes of many diseases, including breast cancer, oral squamous cell carcinoma, and head and neck cancer. However, the mechanism of action of the PTGIS gene in colorectal cancer is not fully understood. This study explored the role of PTGIS in colorectal cancer through comprehensive bioinformatics analysis and in vitro experiments, and found that the expression of PTGIS gene in colorectal cancer tissue was significantly lower than that in normal colorectal tissue (P < 0.05), and high expression of PTGIS gene was associated with poor prognosis in patients (P < 0.05). The KEGG results showed that PTGIS-related genes were mainly enriched in metabolic pathways, arachidonic acid metabolism, steroid biosynthesis, and cancer pathways. The expression of PTGIS may be related to immune infiltration. Cell experiments showed that PTGIS was expressed at a lower level in cancer. Overexpression of PTGIS inhibited apoptosis and promoted proliferation, invasion, and migration ability of SW480 colorectal cancer cells. Analysis of the PTGIS gene in this study provides a theoretical basis for further exploring the pathogenesis of colorectal cancer and finding more accurate new targets for early screening and treatment of the cancer. Nature Publishing Group UK 2023-10-01 /pmc/articles/PMC10543560/ /pubmed/37779109 http://dx.doi.org/10.1038/s41598-023-43289-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ding, Hui
Wang, Kai-yun
Chen, Si-yang
Guo, Kai-Wen
Qiu, Wen-hong
Validating the role of PTGIS gene in colorectal cancer by bioinformatics analysis and in vitro experiments
title Validating the role of PTGIS gene in colorectal cancer by bioinformatics analysis and in vitro experiments
title_full Validating the role of PTGIS gene in colorectal cancer by bioinformatics analysis and in vitro experiments
title_fullStr Validating the role of PTGIS gene in colorectal cancer by bioinformatics analysis and in vitro experiments
title_full_unstemmed Validating the role of PTGIS gene in colorectal cancer by bioinformatics analysis and in vitro experiments
title_short Validating the role of PTGIS gene in colorectal cancer by bioinformatics analysis and in vitro experiments
title_sort validating the role of ptgis gene in colorectal cancer by bioinformatics analysis and in vitro experiments
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543560/
https://www.ncbi.nlm.nih.gov/pubmed/37779109
http://dx.doi.org/10.1038/s41598-023-43289-2
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