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pmid:36237238

Screening and verification of prognostic lncRNA markers related to immune infiltration in the metastasis of osteosarcoma.

Chuan He · Xiaolong Wang · Linying Ni · Chunyu Song · Wei Mai

Translational cancer research · 2022 doi:10.21037/tcr-22-1926

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

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
Screening and verification of prognostic lncRNA markers related to immune infiltration in the metastasis of osteosarcoma.
doi
10.21037/tcr-22-1926
pmid
36237238
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[0]
Chuan He
[1]
Xiaolong Wang
[2]
Linying Ni
[3]
Chunyu Song
[4]
Wei Mai
journal
Translational cancer research
year
2022
abstract
Background: We sought to screen and verify the long non-coding ribonucleic acids (lncRNAs) related to immune infiltration in metastatic osteosarcoma (OS). Methods: We downloaded the RNA-sequencing expression data from The Cancer Genome Atlas (TCGA) database as the training data set. We downloaded the GSE39055 data set from the National Center for Biotechnology Information, Gene Expression Omnibus as the validation data set. The least absolute shrinkage and selection operator (LASSO) regression algorithm was used to screen the optimized lncRNA combinations. Kaplan-Meier curves were used to evaluate the associations between the lncRNAs and actual prognosis. The independent survival prognosis clinical factors were obtained by univariate and multivariate Cox analyses. A nomogram was established to explore the correlation between survival rate and risk information. The Tumor IMmune Estimation Resource was applied to estimate the composition of 6 subtypes of immune infiltration cells. Results: In total, 1,398 lncRNAs and 14,631 messenger RNAs were screened from TCGA data set, and divided into the low and high immunity groups. The Estimation of STromal and Immune cells in MAlignant Tumour tissues using Expression data (ESTIMATE) scores differed significantly between the samples in the two groups. Additionally, 5 optimized lncRNA combinations were obtained using the LASSO algorithm. Risk factors including age, metastatic tumor, and risk-score (RS) were related to the prognosis of OS patients. The survival rates predicted by the nomogram model were consistent with the actual survival rates of OS patients. Finally, we found that RS was negatively correlated with the proportion of immune cells. Conclusions: In total, 5 feature lncRNAs were identified as novel biomarkers for OS. Next, a RS nomogram model was constructed based on the 5 identified lncRNAs. This model predicted the survival rates and prognoses of OS patients well.
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We downloaded the RNA-sequencing expression data from TCGA database, including 265 samples from the Illumina HiSeq 2000 RNA Sequencing platform. After the 265 samples were matched with the clinical information of the OS samples, the samples with information on metastasis were retained. In total, 176 OS samples were included in the analysis, and these were used as the training data set.
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We downloaded the RNA-sequencing expression data from TCGA database, including 265 samples from the Illumina HiSeq 2000 RNA Sequencing platform. After the 265 samples were matched with the clinical information of the OS samples, the samples with information on metastasis were retained. In total, 176 OS samples were included in the analysis, and these were used as the training data set.
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We downloaded the RNA-sequencing expression data from TCGA database, including 265 samples from the Illumina HiSeq 2000 RNA Sequencing platform. After the 265 samples were matched with the clinical information of the OS samples, the samples with information on metastasis were retained. In total, 176 OS samples were included in the analysis, and these were used as the training data set.
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mRNA profiling and clinical outcomes in human osteosarcoma (biopsies)
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We downloaded the GSE39055 data set from the National Center for Biotechnology Information, Gene Expression Omnibus as the validation data set. The least absolute shrinkage and selection operator (LASSO) regression algorithm was used to screen the optimized lncRNA combinations. Kaplan-Meier curves were used to evaluate the associations between the lncRNAs and actual prognosis. The independent survival prognosis clinical factors were obtained by univariate and multivariate Cox analyses. A nomogram was established to explore the correlation between survival rate and risk information. The Tumor IMmune Estimation Resource was applied to estimate the composition of 6 subtypes of immune infiltration cells.\nResults: In total, 1,398 lncRNAs and 14,631 messenger RNAs were screened from TCGA data set, and divided into the low and high immunity groups. 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