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pmid:36077731

Integrative Analysis of Angiogenesis-Related Long Non-Coding RNA and Identification of a Six-DEARlncRNA Signature Associated with Prognosis and Therapeutic Response in Esophageal Squamous Cell Carcinoma.

Shasha Cao · Xiaomin Wang · Xiaohui Liu · Junkuo Li · Lijuan Duan · Zhaowei Gao · Shumin Lun · Yanju Zhu · Haijun Yang · Hao Zhang · Fuyou Zhou

Cancers · 2022 doi:10.3390/cancers14174195

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:36077731
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science-record
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2026-11-01T18:15:18Z
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paper object · 10 fields
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title
Integrative Analysis of Angiogenesis-Related Long Non-Coding RNA and Identification of a Six-DEARlncRNA Signature Associated with Prognosis and Therapeutic Response in Esophageal Squamous Cell Carcinoma.
doi
10.3390/cancers14174195
pmid
36077731
authors array · 11 items
[0]
Shasha Cao
[1]
Xiaomin Wang
[2]
Xiaohui Liu
[3]
Junkuo Li
[4]
Lijuan Duan
[5]
Zhaowei Gao
[6]
Shumin Lun
[7]
Yanju Zhu
[8]
Haijun Yang
[9]
Hao Zhang
[10]
Fuyou Zhou
journal
Cancers
year
2022
abstract
Esophageal squamous cell carcinoma (ESCC) is a lethal gastrointestinal malignancy worldwide. We aimed to identify an angiogenesis-related lncRNAs (ARlncRNAs) signature that could predict the prognosis in ESCC. The GSE53624 and GSE53622 datasets were derived from the GEO database. The differently expressed ARlncRNAs (DEARlncRNAs) were retrieved by the weighted gene co-expression network analysis (WGCNA), differential expression analysis, and correlation analysis. Optimal lncRNA biomarkers were screened from the training set and the six-DEARlncRNA signature comprising AP000696.2, LINC01711, RP11-70C1.3, AP000487.5, AC011997.1, and RP11-225N10.1 could separate patients into high- and low-risk groups with markedly different survival. The validation of the reliability of the risk model was performed by the Kaplan-Meier test, ROC curves, and risk curves in the test set and validation set. Predictive independence analysis indicated that risk score is an independent prognostic biomarker for predicting the prognosis of ESCC patients. Subsequently, a ceRNA regulatory network and functional enrichment analysis were performed. The IC50 test revealed that patients in the high-risk group were resistant to Gefitinib and Lapatinib. Finally, the six DEARlncRNAs were detected by qRT-PCR. In conclusion, we demonstrated a novel ARlncRNA signature as an independent prognostic factor to distinguish the risk of ESCC patients and benefit the personalized clinical applications.
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Our results showed that the six-DEARlncRNA could be used as an effective independent prognostic factor of ESCC.
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Our results showed that the six-DEARlncRNA could be used as an effective independent prognostic factor of ESCC.
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Our results showed that the six-DEARlncRNA could be used as an effective independent prognostic factor of ESCC.
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LncRNA profile study reveals a three-lncRNA signature associated with the survival of esophageal squamous cell carcinoma patients (independent set)
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LncRNA profile study reveals a three-lncRNA signature associated with the survival of esophageal squamous cell carcinoma patients (original)
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agent:corpus-assay-engine
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agent:minimax-reader
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activity-resolve-GSE53622
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agent:corpus-assay-engine
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capability_table_fingerprint
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lineage object · 4 fields
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assays array · 1 item
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Kaplan-Meier
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Complete file
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We aimed to identify an angiogenesis-related lncRNAs (ARlncRNAs) signature that could predict the prognosis in ESCC. The GSE53624 and GSE53622 datasets were derived from the GEO database. The differently expressed ARlncRNAs (DEARlncRNAs) were retrieved by the weighted gene co-expression network analysis (WGCNA), differential expression analysis, and correlation analysis. Optimal lncRNA biomarkers were screened from the training set and the six-DEARlncRNA signature comprising AP000696.2, LINC01711, RP11-70C1.3, AP000487.5, AC011997.1, and RP11-225N10.1 could separate patients into high- and low-risk groups with markedly different survival. The validation of the reliability of the risk model was performed by the Kaplan-Meier test, ROC curves, and risk curves in the test set and validation set. Predictive independence analysis indicated that risk score is an independent prognostic biomarker for predicting the prognosis of ESCC patients. Subsequently, a ceRNA regulatory network and functional enrichment analysis were performed. The IC50 test revealed that patients in the high-risk group were resistant to Gefitinib and Lapatinib. Finally, the six DEARlncRNAs were detected by qRT-PCR. 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