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pmid:38404710

Comprehensive integration of single-cell RNA and transcriptome RNA sequencing to establish a pyroptosis-related signature for improving prognostic prediction of gastric cancer.

Jie Li · Tian Yu · Juan Sun · Mingwei Ma · Zicheng Zheng · Weiming Kang · Xin Ye

Computational and structural biotechnology journal · 2024 doi:10.1016/j.csbj.2024.02.002

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Experiment

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Data

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title
Comprehensive integration of single-cell RNA and transcriptome RNA sequencing to establish a pyroptosis-related signature for improving prognostic prediction of gastric cancer.
doi
10.1016/j.csbj.2024.02.002
pmid
38404710
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Jie Li
[1]
Tian Yu
[2]
Juan Sun
[3]
Mingwei Ma
[4]
Zicheng Zheng
[5]
Weiming Kang
[6]
Xin Ye
journal
Computational and structural biotechnology journal
year
2024
abstract
Cell pyroptosis, a Gasdermin-dependent programmed cell death characterized by inflammasome, plays a complex and dynamic role in Gastric cancer (GC), a serious threat to human health. Therefore, the value of pyroptosis-related genes (PRGs) as prognostic biomarkers and therapeutic indicators for patients needs to be exploited in GC. This study integrates single-cell RNA sequencing (scRNA-seq) dataset GSE183904 with GC transcriptome data from the TCGA database, focusing on the expression and distribution of PRGs in GC at the single-cell level. The prognostic signature of PRGs was established by using Cox and LASSO analyses. The differences in long-term prognosis, immune infiltration, mutation profile, CD274 and response to chemotherapeutic drugs between the two groups were analyzed and evaluated. A tissue array was used to verify the expression of six PRGs, CD274, CD163 and FoxP3. C12orf75, VCAN, RGS2, MKNK2, SOCS3 and TNFAIP2 were successfully screened out to establish a signature to potently predict the survival time of GC patients. A webserver (https://pumc.shinyapps.io/GastricCancer/) for prognostic prediction in GC patients was developed based on this signature. High-risk score patients typically had worse prognoses, resistance to classical chemotherapy, and a more immunosuppressive tumor microenvironment. VCAN, TNFAIP2 and SOCS3 were greatly elevated in the GC while RGS2 and MKNK2 were decreased in the tumor samples. Further, VCAN was positively related to the infiltrations of Tregs and M2 TAMs in GC TME and the CD274 in tumor cells. In summary, a potent pyroptosis-related signature was established to accurately forecast the survival time and treatment responsiveness of GC patients.
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Univariate Cox analysis was used to preliminarily identify PRGs associated with the overall survival (OS) of GC patients. Subsequently, LASSO analysis was used to screen out the prominent genes, and multivariate Cox analysis was further used to construct a prognostic signature.
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sections[9] "Construction of a prognostic signature" paragraph 2
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Univariate Cox analysis was used to preliminarily identify PRGs associated with the overall survival (OS) of GC patients. Subsequently, LASSO analysis was used to screen out the prominent genes, and multivariate Cox analysis was further used to construct a prognostic signature.
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In this study, we selected 24 primary gastric cancer tumor samples from the GSE183904 dataset [18].
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In this study, we selected 24 primary gastric cancer tumor samples from the GSE183904 dataset [18].
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Then, LASSO and multivariate Cox analysis were used to screen out the 6 prominent genes (C12orf75, VCAN, RGS2, MKNK2, SOCS3 and TNFAIP2), and calculate the coefficient of each gene in formula of risk score (Figs. 5A and 5B).
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sections[21] "Construction and validation of prognostic models based on PRGs" paragraph 2
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Then, LASSO and multivariate Cox analysis were used to screen out the 6 prominent genes (C12orf75, VCAN, RGS2, MKNK2, SOCS3 and TNFAIP2), and calculate the coefficient of each gene in formula of risk score (Figs. 5A and 5B).
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Then, LASSO and multivariate Cox analysis were used to screen out the 6 prominent genes (C12orf75, VCAN, RGS2, MKNK2, SOCS3 and TNFAIP2), and calculate the coefficient of each gene in formula of risk score (Figs. 5A and 5B).
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The paper names GSE183904, GSE62254 in GSE183904 dataset and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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gration of single-cell RNA and transcriptome RNA sequencing to establish a pyroptosis-related signature
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ted in GC. This study integrates single-cell RNA sequencing (scRNA-seq) dataset GSE183904 with GC transc
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rehensive integration of single-cell RNA and transcriptome RNA sequencing to establish a pyroptosis-rel
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to be exploited in GC. This study integrates single-cell RNA sequencing (scRNA-seq) dataset GSE183904 with GC transc
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study integrates single-cell RNA sequencing (scRNA-seq) dataset GSE183904 with GC transcriptome dat
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Therefore, the value of pyroptosis-related genes (PRGs) as prognostic biomarkers and therapeutic indicators for patients needs to be exploited in GC. This study integrates single-cell RNA sequencing (scRNA-seq) dataset GSE183904 with GC transcriptome data from the TCGA database, focusing on the expression and distribution of PRGs in GC at the single-cell level. The prognostic signature of PRGs was established by using Cox and LASSO analyses. The differences in long-term prognosis, immune infiltration, mutation profile, CD274 and response to chemotherapeutic drugs between the two groups were analyzed and evaluated. A tissue array was used to verify the expression of six PRGs, CD274, CD163 and FoxP3. C12orf75, VCAN, RGS2, MKNK2, SOCS3 and TNFAIP2 were successfully screened out to establish a signature to potently predict the survival time of GC patients. A webserver (https://pumc.shinyapps.io/GastricCancer/) for prognostic prediction in GC patients was developed based on this signature. High-risk score patients typically had worse prognoses, resistance to classical chemotherapy, and a more immunosuppressive tumor microenvironment. VCAN, TNFAIP2 and SOCS3 were greatly elevated in the GC while RGS2 and MKNK2 were decreased in the tumor samples. Further, VCAN was positively related to the infiltrations of Tregs and M2 TAMs in GC TME and the CD274 in tumor cells. In summary, a potent pyroptosis-related signature was established to accurately forecast the survival time and treatment responsiveness of GC patients.", "claims": [{"id": "claim-method", "statement": "Univariate Cox analysis was used to preliminarily identify PRGs associated with the overall survival (OS) of GC patients. 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