Integrated single-cell and bulk RNA sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancer

Abstract Ferroptosis is an iron-dependent form of cell death induced by lipid oxidation with an essential role in diseases, including cancer. Since prognostic value of ferroptosis-dependent related genes (FDRGs) in colorectal cancer (CRC) remains unclear, we explored the significance of FDRGs in CRC...

Full description

Bibliographic Details
Main Authors: Xiaochen Xu, Xinwen Zhang, Qiumei Lin, Yuling Qin, Yihao Liu, Weizhong Tang
Format: Article
Language:English
Published: Nature Portfolio 2023-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-39412-y
_version_ 1797576790794829824
author Xiaochen Xu
Xinwen Zhang
Qiumei Lin
Yuling Qin
Yihao Liu
Weizhong Tang
author_facet Xiaochen Xu
Xinwen Zhang
Qiumei Lin
Yuling Qin
Yihao Liu
Weizhong Tang
author_sort Xiaochen Xu
collection DOAJ
description Abstract Ferroptosis is an iron-dependent form of cell death induced by lipid oxidation with an essential role in diseases, including cancer. Since prognostic value of ferroptosis-dependent related genes (FDRGs) in colorectal cancer (CRC) remains unclear, we explored the significance of FDRGs in CRC through comprehensive single-cell analysis. We downloaded the GSE161277 dataset for single-cell analyses and calculated the ferroptosis-dependent gene score (FerrScore) for each cell type. According to each cell type-specific median FerrScore, we categorized the cells into low- and high-ferroptosis groups. By analyzing differentially-expressed genes across the two groups, we identified FDRGs. We further screened these prognosis-related genes used to develop a prognostic signature and calculated its correlation with immune infiltration. We also compared immune checkpoint gene efficacy among different risk groups, and qRT-PCR was performed in colorectal normal and cancer cell lines to explore whether the signature genes could be used as clinical prognostic indicators. In total, 523 FDRGs were identified. A prognostic signature including five signature genes was constructed, and patients were divided into two risk groups. The high-risk group had poor survival rates and displayed high levels of immune infiltration. Our newly developed ferroptosis-based prognostic signature possessed a high predictive ability for CRC.
first_indexed 2024-03-10T21:57:46Z
format Article
id doaj.art-bae51d5875a04ff380c7cc310cd440b1
institution Directory Open Access Journal
issn 2045-2322
language English
last_indexed 2024-03-10T21:57:46Z
publishDate 2023-08-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj.art-bae51d5875a04ff380c7cc310cd440b12023-11-19T13:03:37ZengNature PortfolioScientific Reports2045-23222023-08-0113111410.1038/s41598-023-39412-yIntegrated single-cell and bulk RNA sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancerXiaochen Xu0Xinwen Zhang1Qiumei Lin2Yuling Qin3Yihao Liu4Weizhong Tang5Department of Gastrointestinal Surgery, Guangxi Medical University Cancer HospitalDepartment of Gastrointestinal Surgery, Affiliated Hospital of Guilin Medical UniversityDepartment of Clinical Laboratory, Guangxi Medical University Cancer HospitalDepartment of Clinical Laboratory, Guangxi Medical University Cancer HospitalDepartment of Gastrointestinal Surgery, Affiliated Hospital of Guilin Medical UniversityDepartment of Gastrointestinal Surgery, Guangxi Medical University Cancer HospitalAbstract Ferroptosis is an iron-dependent form of cell death induced by lipid oxidation with an essential role in diseases, including cancer. Since prognostic value of ferroptosis-dependent related genes (FDRGs) in colorectal cancer (CRC) remains unclear, we explored the significance of FDRGs in CRC through comprehensive single-cell analysis. We downloaded the GSE161277 dataset for single-cell analyses and calculated the ferroptosis-dependent gene score (FerrScore) for each cell type. According to each cell type-specific median FerrScore, we categorized the cells into low- and high-ferroptosis groups. By analyzing differentially-expressed genes across the two groups, we identified FDRGs. We further screened these prognosis-related genes used to develop a prognostic signature and calculated its correlation with immune infiltration. We also compared immune checkpoint gene efficacy among different risk groups, and qRT-PCR was performed in colorectal normal and cancer cell lines to explore whether the signature genes could be used as clinical prognostic indicators. In total, 523 FDRGs were identified. A prognostic signature including five signature genes was constructed, and patients were divided into two risk groups. The high-risk group had poor survival rates and displayed high levels of immune infiltration. Our newly developed ferroptosis-based prognostic signature possessed a high predictive ability for CRC.https://doi.org/10.1038/s41598-023-39412-y
spellingShingle Xiaochen Xu
Xinwen Zhang
Qiumei Lin
Yuling Qin
Yihao Liu
Weizhong Tang
Integrated single-cell and bulk RNA sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancer
Scientific Reports
title Integrated single-cell and bulk RNA sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancer
title_full Integrated single-cell and bulk RNA sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancer
title_fullStr Integrated single-cell and bulk RNA sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancer
title_full_unstemmed Integrated single-cell and bulk RNA sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancer
title_short Integrated single-cell and bulk RNA sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancer
title_sort integrated single cell and bulk rna sequencing analysis identifies a prognostic signature related to ferroptosis dependence in colorectal cancer
url https://doi.org/10.1038/s41598-023-39412-y
work_keys_str_mv AT xiaochenxu integratedsinglecellandbulkrnasequencinganalysisidentifiesaprognosticsignaturerelatedtoferroptosisdependenceincolorectalcancer
AT xinwenzhang integratedsinglecellandbulkrnasequencinganalysisidentifiesaprognosticsignaturerelatedtoferroptosisdependenceincolorectalcancer
AT qiumeilin integratedsinglecellandbulkrnasequencinganalysisidentifiesaprognosticsignaturerelatedtoferroptosisdependenceincolorectalcancer
AT yulingqin integratedsinglecellandbulkrnasequencinganalysisidentifiesaprognosticsignaturerelatedtoferroptosisdependenceincolorectalcancer
AT yihaoliu integratedsinglecellandbulkrnasequencinganalysisidentifiesaprognosticsignaturerelatedtoferroptosisdependenceincolorectalcancer
AT weizhongtang integratedsinglecellandbulkrnasequencinganalysisidentifiesaprognosticsignaturerelatedtoferroptosisdependenceincolorectalcancer