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Mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer
The Notch signalling pathway is involved in the development of several cancers, including colorectal cancer (CRC). However, whether mutations in this pathway could alter the CRC immunophenotype remains unknown. Here, we investigated the relationship between Notch signalling pathway mutations and the...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579712/ https://www.ncbi.nlm.nih.gov/pubmed/32924269 http://dx.doi.org/10.1111/jcmm.15867 |
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author | Wang, Fei Long, Jie Li, Liang Zhao, Zhi‐bin Wei, Fang Yao, Yuan Qiu, Wen‐Jing Wu, Zi‐Xin Luo, Qing‐Qing Liu, Wei Quan, Yi‐Bo Lian, Zhe‐Xiong Cao, Jie |
author_facet | Wang, Fei Long, Jie Li, Liang Zhao, Zhi‐bin Wei, Fang Yao, Yuan Qiu, Wen‐Jing Wu, Zi‐Xin Luo, Qing‐Qing Liu, Wei Quan, Yi‐Bo Lian, Zhe‐Xiong Cao, Jie |
author_sort | Wang, Fei |
collection | PubMed |
description | The Notch signalling pathway is involved in the development of several cancers, including colorectal cancer (CRC). However, whether mutations in this pathway could alter the CRC immunophenotype remains unknown. Here, we investigated the relationship between Notch signalling pathway mutations and the tumour immune microenvironment by analysing gene expression data from the GSE108989 single T cell RNA sequencing data set and The Cancer Genome Atlas (TCGA) data set. We found that Notch signalling pathway mutations were associated with an increased number of tumour‐specific CD8(+) T cells and decreased number of inhibitory regulatory T (Treg) cells, representing an enhanced anti‐tumour response in the GSE108989 data set. In TCGA data set, we also found that Notch signalling pathway mutations were associated with enrichment of genes associated with immune activation pathways and higher expressions of PDCD1, GZMB and PRF1. Although Notch signalling pathway mutations did not affect the overall survival and disease‐free survival of CRC patients, they were associated with earlier disease stages and lower rates of metastasis. These results demonstrated that Notch signalling pathway mutations can enhance anti‐tumour immunity in CRC, as validated by the two data sets, suggesting that they may be promising biomarkers for immune checkpoint blockade therapies for CRC patients. |
format | Online Article Text |
id | pubmed-7579712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75797122020-10-27 Mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer Wang, Fei Long, Jie Li, Liang Zhao, Zhi‐bin Wei, Fang Yao, Yuan Qiu, Wen‐Jing Wu, Zi‐Xin Luo, Qing‐Qing Liu, Wei Quan, Yi‐Bo Lian, Zhe‐Xiong Cao, Jie J Cell Mol Med Original Articles The Notch signalling pathway is involved in the development of several cancers, including colorectal cancer (CRC). However, whether mutations in this pathway could alter the CRC immunophenotype remains unknown. Here, we investigated the relationship between Notch signalling pathway mutations and the tumour immune microenvironment by analysing gene expression data from the GSE108989 single T cell RNA sequencing data set and The Cancer Genome Atlas (TCGA) data set. We found that Notch signalling pathway mutations were associated with an increased number of tumour‐specific CD8(+) T cells and decreased number of inhibitory regulatory T (Treg) cells, representing an enhanced anti‐tumour response in the GSE108989 data set. In TCGA data set, we also found that Notch signalling pathway mutations were associated with enrichment of genes associated with immune activation pathways and higher expressions of PDCD1, GZMB and PRF1. Although Notch signalling pathway mutations did not affect the overall survival and disease‐free survival of CRC patients, they were associated with earlier disease stages and lower rates of metastasis. These results demonstrated that Notch signalling pathway mutations can enhance anti‐tumour immunity in CRC, as validated by the two data sets, suggesting that they may be promising biomarkers for immune checkpoint blockade therapies for CRC patients. John Wiley and Sons Inc. 2020-09-14 2020-10 /pmc/articles/PMC7579712/ /pubmed/32924269 http://dx.doi.org/10.1111/jcmm.15867 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Wang, Fei Long, Jie Li, Liang Zhao, Zhi‐bin Wei, Fang Yao, Yuan Qiu, Wen‐Jing Wu, Zi‐Xin Luo, Qing‐Qing Liu, Wei Quan, Yi‐Bo Lian, Zhe‐Xiong Cao, Jie Mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer |
title | Mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer |
title_full | Mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer |
title_fullStr | Mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer |
title_full_unstemmed | Mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer |
title_short | Mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer |
title_sort | mutations in the notch signalling pathway are associated with enhanced anti‐tumour immunity in colorectal cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579712/ https://www.ncbi.nlm.nih.gov/pubmed/32924269 http://dx.doi.org/10.1111/jcmm.15867 |
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