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pmid:36072903
Epithelial-Mesenchymal Transition Gene Signature Is Associated with Neoadjuvant Chemoradiotherapy Resistance and Prognosis of Esophageal Squamous Cell Carcinoma.
Kewei Song · Baohong Gu · Chenhui Ma · Bofang Wang · Na Wang · Rong Yu · Hao Chen
Disease markers · 2022 doi:10.1155/2022/3534433
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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However, the benefits of neo-CRT are diverse among patients. Consequently, the development of new biomarkers that correlate with neo-CRT might be important for the treatment of ESCC.\nMethods: The differentially expressed genes (DEG) between responsive and resistant samples from the GSE45670 dataset were obtained. On the TCGA dataset, survival analysis was performed to identify prognosis-related-EMT-genes. For EMT score model construction, lasso regression analysis in the TCGA cohort was used to identify the genes. In the TCGA-ESCC cohort, age, stage, and EMT score were used to construct a nomogram.\nResults: In total, 10 prognosis-related-EMT-genes were obtained. These 10 genes consisted of 6 risky genes and 4 protective genes. Based on the lasso analysis and univariate Cox regression, an EMT score model consisting of 7 genes (CLEC18A, PIR, KCNN4, MST1R, CAPG, ALDH5A1, and COX7B) was identified. ESCC patients with a high EMT score have a worse prognosis. These genes were differentially expressed between responsive and resistant patients and had a high accuracy for distinguishing resistant and responsive patients.\nConclusions: The identified genes have the potential to function as molecular biomarkers for predicting ESCC patients' resistance to neo-CRT. This research may aid in the elucidation of the molecular processes driving resistance and the identification of targets for improving the prognosis for ESCC.", "claims": [{"id": "claim-method", "statement": "We have determined the candidate prognostic genes by applying lasso regression analysis in the TCGA-ESCC cohort by using the glmnet package [28]. We then used univariate Cox regression analysis to calculate the coefficients for each gene.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36072903", "locator": "sections[6] \"2.4. 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