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pmid:39430816
Telomere-related prognostic signature for survival assessments in lung adenocarcinoma.
Hong Lin · Weiguo Yin
Translational cancer research · 2024 doi:10.21037/tcr-24-767
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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This study is to investigate the prognostic value of TRGs in LUAD and to develop a TRG signature that can predict patient survival.\nMethods: A total of 2,086 TRGs were obtained from a database of genes involved in telomere maintenance (TelNet), while the clinical information and tumor RNA expression profiles of 513 LUAD patients were acquired from The Cancer Genome Atlas (TCGA) database. Statistical methodologies, such as least absolute shrinkage and selection operator (LASSO)-Cox, were employed to construct a prognostic model with predictive capabilities.\nResults: We analyzed 1,339 telomere-associated differentially expressed genes and identified a ten-gene predictive signature for LUAD. This signature exhibited effective prognostic classification capabilities across multiple datasets, including GSE3141 (58 samples), GSE8894 (63 samples), GSE50081 (127 samples), and GSE72094 (398 samples). Furthermore, we screened tumor-sensitive drugs targeting this signature. High telomere levels were associated with reduced survival in lung cancer patients who underwent surgery. Compared to the traditional TNM (tumor node metastasis classification) grading method, our telomere-associated gene panel demonstrated superior prediction accuracy. Notably, patients in the high-risk group, defined by the telomere-associated signature, exhibited improved responses to immunotherapy, suggesting potential benefits for this subgroup of patients.\nConclusions: This study presents a comprehensive molecular signature comprising TRGs, which holds potential for functional and therapeutic investigations. Additionally, it serves as an integrated tool to identify crucial molecules for immunotherapy in lung cancer.", "claims": [{"id": "claim-method", "statement": "Statistical methodologies, such as least absolute shrinkage and selection operator (LASSO)-Cox, were employed to construct a prognostic model with predictive capabilities.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39430816", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Statistical methodologies, such as least absolute shrinkage and selection operator (LASSO)-Cox, were employed to construct a prognostic model with predictive capabilities."}], "state": "complete"}, {"id": "claim-data-access", "statement": "We used The Cancer Genome Atlas (TCGA) (15) to obtain RNA-seq data and clinical information for LUAD patients, providing a reliable basis for conducting thorough genomic and clinical analysis.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39430816", "locator": "sections[4] \"Data sources and study population\" paragraph 2", "quote": "We used The Cancer Genome Atlas (TCGA) (15) to obtain RNA-seq data and clinical information for LUAD patients, providing a reliable basis for conducting thorough genomic and clinical analysis."}], "state": "complete"}, {"id": "claim-target-result", "statement": "A ten-gene prognostic signature based on 1,339 telomere-associated differentially expressed genes was developed and validated as a survival-prediction tool for lung adenocarcinoma.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:39430816", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "We analyzed 1,339 telomere-associated differentially expressed genes and identified a ten-gene predictive signature for LUAD."}, {"asset": "source:pmid:39430816", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "This signature exhibited effective prognostic classification capabilities across multiple datasets, including GSE3141 (58 samples), GSE8894 (63 samples), GSE50081 (127 samples), and GSE72094 (398 samples)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "A ten-gene prognostic signature based on 1,339 telomere-associated differentially expressed genes was developed and validated as a survival-prediction tool for lung adenocarcinoma.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:39430816"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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