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Pathologic evolution-related Gene Analysis based on both single-cell and bulk transcriptomics in Colorectal Cancer
Purpose: The patients diagnosed with colorectal cancer (CRC) are likely to undergo differential outcomes in clinical survival owing to different pathologic stages. However, signatures in association with pathologic evolution and CRC prognosis are not clearly defined. This study aimed to identify pat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591993/ https://www.ncbi.nlm.nih.gov/pubmed/33123277 http://dx.doi.org/10.7150/jca.49262 |
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author | Li, Jiali Zeng, Zihang Chen, Jiarui Liu, Xingyu Jiang, Xueping Sun, Wenjie Luo, Yuan Ren, Jiangbo Gong, Yan Xie, Conghua |
author_facet | Li, Jiali Zeng, Zihang Chen, Jiarui Liu, Xingyu Jiang, Xueping Sun, Wenjie Luo, Yuan Ren, Jiangbo Gong, Yan Xie, Conghua |
author_sort | Li, Jiali |
collection | PubMed |
description | Purpose: The patients diagnosed with colorectal cancer (CRC) are likely to undergo differential outcomes in clinical survival owing to different pathologic stages. However, signatures in association with pathologic evolution and CRC prognosis are not clearly defined. This study aimed to identify pathologic evolution-related genes in CRC based on both single-cell and bulk transcriptomics. Patients and methods: The CRC single-cell transcriptomic dataset (GSE81861, n=590) with clinical information and tumor microenvironmental tissues was collected to identify the pathologic evolution-related genes. The colonic adenocarcinoma and rectum adenocarcinoma transcriptomics from The Cancer Genome Atlas were obtained as the training dataset (n=363) and 5 other CRC transcriptomics cohorts from Gene Expression Omnibus (n=1031) were acquired as validation data. Graph-based clustering analysis algorithm was applied to identify pathologic evolution-related cell populations. Pseudotime analysis was performed to construct the trajectory plot of pathologic evolution and to define hub genes in the evolution process. Cell-type identification by estimating relative subsets of RNA transcripts was then executed to build a novel cell infiltration classifier. The prediction efficacy of this classifier was validated in bulk transcriptomic datasets. Results: Epithelial and T cells were elucidated to be related to the pathologic stages in CRC tissues. Pseudotime analysis and survival analysis indicated that HOXC5, HOXC8 and BMP5 were the marker genes in pathologic evolution process. Our cell infiltration classifier exhibited excellent forecast efficacy in predicting pathologic stages and prognosis of CRC patients. Conclusion: We identified pathologic evolution-related genes in single-cell transcriptomic and proposed a novel specific cell infiltration classifier to forecast the prognosis of CRC patients based on pathologic stage-related hub genes HOXC6, HOXC8 and BMP5. |
format | Online Article Text |
id | pubmed-7591993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-75919932020-10-28 Pathologic evolution-related Gene Analysis based on both single-cell and bulk transcriptomics in Colorectal Cancer Li, Jiali Zeng, Zihang Chen, Jiarui Liu, Xingyu Jiang, Xueping Sun, Wenjie Luo, Yuan Ren, Jiangbo Gong, Yan Xie, Conghua J Cancer Research Paper Purpose: The patients diagnosed with colorectal cancer (CRC) are likely to undergo differential outcomes in clinical survival owing to different pathologic stages. However, signatures in association with pathologic evolution and CRC prognosis are not clearly defined. This study aimed to identify pathologic evolution-related genes in CRC based on both single-cell and bulk transcriptomics. Patients and methods: The CRC single-cell transcriptomic dataset (GSE81861, n=590) with clinical information and tumor microenvironmental tissues was collected to identify the pathologic evolution-related genes. The colonic adenocarcinoma and rectum adenocarcinoma transcriptomics from The Cancer Genome Atlas were obtained as the training dataset (n=363) and 5 other CRC transcriptomics cohorts from Gene Expression Omnibus (n=1031) were acquired as validation data. Graph-based clustering analysis algorithm was applied to identify pathologic evolution-related cell populations. Pseudotime analysis was performed to construct the trajectory plot of pathologic evolution and to define hub genes in the evolution process. Cell-type identification by estimating relative subsets of RNA transcripts was then executed to build a novel cell infiltration classifier. The prediction efficacy of this classifier was validated in bulk transcriptomic datasets. Results: Epithelial and T cells were elucidated to be related to the pathologic stages in CRC tissues. Pseudotime analysis and survival analysis indicated that HOXC5, HOXC8 and BMP5 were the marker genes in pathologic evolution process. Our cell infiltration classifier exhibited excellent forecast efficacy in predicting pathologic stages and prognosis of CRC patients. Conclusion: We identified pathologic evolution-related genes in single-cell transcriptomic and proposed a novel specific cell infiltration classifier to forecast the prognosis of CRC patients based on pathologic stage-related hub genes HOXC6, HOXC8 and BMP5. Ivyspring International Publisher 2020-10-22 /pmc/articles/PMC7591993/ /pubmed/33123277 http://dx.doi.org/10.7150/jca.49262 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Li, Jiali Zeng, Zihang Chen, Jiarui Liu, Xingyu Jiang, Xueping Sun, Wenjie Luo, Yuan Ren, Jiangbo Gong, Yan Xie, Conghua Pathologic evolution-related Gene Analysis based on both single-cell and bulk transcriptomics in Colorectal Cancer |
title | Pathologic evolution-related Gene Analysis based on both single-cell and bulk transcriptomics in Colorectal Cancer |
title_full | Pathologic evolution-related Gene Analysis based on both single-cell and bulk transcriptomics in Colorectal Cancer |
title_fullStr | Pathologic evolution-related Gene Analysis based on both single-cell and bulk transcriptomics in Colorectal Cancer |
title_full_unstemmed | Pathologic evolution-related Gene Analysis based on both single-cell and bulk transcriptomics in Colorectal Cancer |
title_short | Pathologic evolution-related Gene Analysis based on both single-cell and bulk transcriptomics in Colorectal Cancer |
title_sort | pathologic evolution-related gene analysis based on both single-cell and bulk transcriptomics in colorectal cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591993/ https://www.ncbi.nlm.nih.gov/pubmed/33123277 http://dx.doi.org/10.7150/jca.49262 |
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