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pmid:34735373

A prognostic fibroblast-related risk signature in colorectal cancer.

Hao Xu · Yisheng Pan

Aging · 2021 doi:10.18632/aging.203677

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

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pmid:34735373
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title
A prognostic fibroblast-related risk signature in colorectal cancer.
doi
10.18632/aging.203677
pmid
34735373
authors array · 2 items
[0]
Hao Xu
[1]
Yisheng Pan
journal
Aging
year
2021
abstract
Colorectal cancer (CRC) is the third most common cancer in the world. The accessibility of the Cancer Genome Atlas (TCGA) and Gene Expression Omnibus data allows the prognostic evaluation of CRC. Fibroblasts play a key role in the development and progression of tumors while fibroblast-related risk signature in CRC patients has rarely been mentioned. In this study, TCGA data was classified into high-fibroblast and low-fibroblast groups according to the median of fibroblast content. Among 3845 differentially expressed genes between two groups, 14 prognostic genes commonly expressed in GSE39582 and TCGA were identified by LASSO-COX analysis. Then we established a fibroblast-related risk signature in TCGA training group and validated in the GSE39582 testing group. The risk score was significantly associated with the overall survival (OS), and the poor prognosis of patients in high-risk group might relate to the immune cell infiltration in the tumor microenvironment, epithelial-mesenchymal transition, and extracellular matrix related processes. Overall, we proved that the fibroblast-related signature could predict the prognosis of patients which might shed light on the treatment of CRC.
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Univariate Cox was used to obtain 222 prognostic genes in training set through traversing all DEGs in fibroblast high/low condition, and LASSO-penalized Cox regression was used to construct optimal prognostic risk signatures in training group. R package survival and survminer were applied to investigate the difference of prognosis between two groups by log-rank test.
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sections[7] "Development and validation of the prognostic signature" paragraph 2
quote
Univariate Cox was used to obtain 222 prognostic genes in training set through traversing all DEGs in fibroblast high/low condition, and LASSO-penalized Cox regression was used to construct optimal prognostic risk signatures in training group.
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sections[8] "Survival analysis" paragraph 2
quote
R package survival and survminer were applied to investigate the difference of prognosis between two groups by log-rank test.
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sections[12] "Data availability statement" paragraph 2
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All data for this study are available from the corresponding public database.
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The study established a 14-gene fibroblast-related risk signature whose risk score was significantly associated with overall survival in the TCGA training cohort and the GSE39582 testing cohort.
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sections[15] "Development of a fibroblast-related risk signature" paragraph 2
quote
Then 14 genes identified by LASSO-COX analysis were used to establish a fibroblast-related risk signature of CRC in TCGA.
[1] object · 3 fields
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source:pmid:34735373
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sections[15] "Development of a fibroblast-related risk signature" paragraph 2
quote
The results confirmed that the fibroblast-related risk signature was significantly associated with the OS of CRC patients in the testing group (Figure 2E).
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The study established a 14-gene fibroblast-related risk signature whose risk score was significantly associated with overall survival in the TCGA training cohort and the GSE39582 testing cohort.
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sample_count
585
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics [Expression]
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2026-11-01T15:39:54Z
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Univariate Cox was used to obtain 222 prognostic genes in training set through traversing all DEGs in fibroblast high/low condition, and LASSO-penalized Cox regression was used to construct optimal prognostic risk signatures in training group. R package survival and survminer were applied to investigate the difference of prognosis between two groups by log-rank test.
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Automated Assays Laravel application and simulated adapters
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
capability object · 4 fields
tier
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capability_id
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availability_state
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The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
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All data for this study are available from the corresponding public database.
basis
The paper names GSE39582 in NCBI Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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minimax
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GEO GSE39582
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Univariate Cox was used to obtain 222 prognostic genes in training set through traversing all DEGs in fibroblast high/low condition, and LASSO-penalized Cox regression was used to construct optimal prognostic risk signatures in training group. R package survival and survminer were applied to investigate the difference of prognosis between two groups by log-rank test.
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Complete file
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Fibroblasts play a key role in the development and progression of tumors while fibroblast-related risk signature in CRC patients has rarely been mentioned. In this study, TCGA data was classified into high-fibroblast and low-fibroblast groups according to the median of fibroblast content. Among 3845 differentially expressed genes between two groups, 14 prognostic genes commonly expressed in GSE39582 and TCGA were identified by LASSO-COX analysis. Then we established a fibroblast-related risk signature in TCGA training group and validated in the GSE39582 testing group. The risk score was significantly associated with the overall survival (OS), and the poor prognosis of patients in high-risk group might relate to the immune cell infiltration in the tumor microenvironment, epithelial-mesenchymal transition, and extracellular matrix related processes. 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