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pmid:38684858

Importance of CD8 Tex cell-associated gene signatures in the prognosis and immunology of osteosarcoma.

Yining Lu · Nana Cao · Ming Zhao · Guochuan Zhang · Qi Zhang · Ling Wang

Scientific reports · 2024 doi:10.1038/s41598-024-60539-z

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complete

Experiment

complete

Data

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Analysis

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absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Importance of CD8 Tex cell-associated gene signatures in the prognosis and immunology of osteosarcoma.
doi
10.1038/s41598-024-60539-z
pmid
38684858
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[0]
Yining Lu
[1]
Nana Cao
[2]
Ming Zhao
[3]
Guochuan Zhang
[4]
Qi Zhang
[5]
Ling Wang
journal
Scientific reports
year
2024
abstract
As a highly aggressive bone malignancy, osteosarcoma poses a significant therapeutic challenge, especially in the setting of metastasis or recurrence. This study aimed to investigate the potential of CD8-Tex cell-associated genes as prognostic biomarkers to reveal the immunogenomic profile of osteosarcoma and guide therapeutic decisions. mRNA expression data and clinical details of osteosarcoma patients were obtained from the TCGA database (TARGET-OS dataset). The GSE21257 dataset (from the GEO database) was used as an external validation set to provide additional information on osteosarcoma specimens. 84 samples from the TARGET-OS dataset were used as the training set, and 53 samples from the GSE21257 dataset served as the external validation cohort. Univariate Cox regression analysis was utilized to identify CD8 Tex cell genes associated with prognosis. The LASSO algorithm was performed for 1000 iterations to select the best subset to form the CD8 Tex cell gene signature (TRS). Final genes were identified using the multivariate Cox regression model of the LASSO algorithm. Risk scores were calculated to categorize patients into high- and low-risk groups, and clinical differences were explored by Kaplan-Meier survival analysis to assess model performance. Prediction maps were constructed to estimate 1-, 3-, and 5 year survival rates for osteosarcoma patients, including risk scores for CD8 Texcell gene markers and clinicopathologic factors. The ssGSEA algorithm was used to assess the differences in immune function between TRS-defined high- and low-risk groups. TME and immune cell infiltration were further assessed using the ESTIMATE and CIBERSORT algorithms. To explore the relationship between immune checkpoint gene expression levels and the two risk-defined groups. A CD8 Tex cell-associated gene signature was extracted from the TISCH database and prognostic markers including two genes were developed. The high-risk group showed lower survival, and model performance was validated by ROC curves and C-index. Predictive plots were constructed to demonstrate survival estimates, combining CD8 Tex cell gene markers and clinical factors. This study provides valuable insights into the molecular and immune characteristics of osteosarcoma and offers potential avenues for advances in therapeutic approaches.
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Using the LASSO Cox regression model to select the optimal subset of prognostic genes, by iterating the LASSO algorithm 1000 times in the training set, we identified the optimal subset of genes that form the CD8 Tex cell gene signature (TRS).
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sections[12] "Development of prognostic genes signature" paragraph 2
quote
Using the LASSO Cox regression model to select the optimal subset of prognostic genes, by iterating the LASSO algorithm 1000 times in the training set, we identified the optimal subset of genes that form the CD8 Tex cell gene signature (TRS).
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As shown in Fig. 1, we searched the single-cell RNA sequencing data of osteosarcoma in the TISCH database (GSE162454) and extracted differential genes for the CD8Tex cell population.
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sections[3] "Extraction of CD8 Tex cell-associated gene signature" paragraph 2
quote
As shown in Fig. 1, we searched the single-cell RNA sequencing data of osteosarcoma in the TISCH database (GSE162454) and extracted differential genes for the CD8Tex cell population.
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A two-gene CD8 Tex cell-associated prognostic signature, comprising GJA1 and HLA-DQA1, was developed, and the high-risk group showed lower survival.
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sections[3] "Extraction of CD8 Tex cell-associated gene signature" paragraph 2
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After applying the LASSO algorithm, a multivariate Cox regression model was used to identify the final gene set, which consisted of two robust genes (GJA1 and HLA-DQA1) that formed a prognostic signature for overall survival (Fig. 2).
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The high-risk group showed lower survival, and model performance was validated by ROC curves and C-index.
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A two-gene CD8 Tex cell-associated prognostic signature, comprising GJA1 and HLA-DQA1, was developed, and the high-risk group showed lower survival.
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Using the LASSO Cox regression model to select the optimal subset of prognostic genes, by iterating the LASSO algorithm 1000 times in the training set, we identified the optimal subset of genes that form the CD8 Tex cell gene signature (TRS).
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Using the LASSO Cox regression model to select the optimal subset of prognostic genes, by iterating the LASSO algorithm 1000 times in the training set, we identified the optimal subset of genes that form the CD8 Tex cell gene signature (TRS).
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Complete file
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This study aimed to investigate the potential of CD8-Tex cell-associated genes as prognostic biomarkers to reveal the immunogenomic profile of osteosarcoma and guide therapeutic decisions. mRNA expression data and clinical details of osteosarcoma patients were obtained from the TCGA database (TARGET-OS dataset). The GSE21257 dataset (from the GEO database) was used as an external validation set to provide additional information on osteosarcoma specimens. 84 samples from the TARGET-OS dataset were used as the training set, and 53 samples from the GSE21257 dataset served as the external validation cohort. Univariate Cox regression analysis was utilized to identify CD8 Tex cell genes associated with prognosis. The LASSO algorithm was performed for 1000 iterations to select the best subset to form the CD8 Tex cell gene signature (TRS). Final genes were identified using the multivariate Cox regression model of the LASSO algorithm. Risk scores were calculated to categorize patients into high- and low-risk groups, and clinical differences were explored by Kaplan-Meier survival analysis to assess model performance. Prediction maps were constructed to estimate 1-, 3-, and 5 year survival rates for osteosarcoma patients, including risk scores for CD8 Texcell gene markers and clinicopathologic factors. The ssGSEA algorithm was used to assess the differences in immune function between TRS-defined high- and low-risk groups. TME and immune cell infiltration were further assessed using the ESTIMATE and CIBERSORT algorithms. To explore the relationship between immune checkpoint gene expression levels and the two risk-defined groups. A CD8 Tex cell-associated gene signature was extracted from the TISCH database and prognostic markers including two genes were developed. The high-risk group showed lower survival, and model performance was validated by ROC curves and C-index. Predictive plots were constructed to demonstrate survival estimates, combining CD8 Tex cell gene markers and clinical factors. 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