Published online Nov 26, 2022. doi: 10.12998/wjcc.v10.i33.12089
Peer-review started: June 18, 2022
First decision: August 6, 2022
Revised: August 18, 2022
Accepted: October 9, 2022
Article in press: October 9, 2022
Published online: November 26, 2022
Processing time: 157 Days and 18.5 Hours
Despite many breakthroughs in treatment, the general prognosis for esophageal cancer, one of the least responsive malignancies to cancer therapy, remains poor. As a result, identifying biomarkers and understanding the molecular mechanisms of esophageal cancer were critical for improving patient outcomes.
A nomogram for predicting the prognosis of esophageal cancer would be developed by evaluating cuproprosis-related genes features and their correlation with prognosis in order to predict the prognosis of esophageal cancer.
Considering cuproprosis-related genes expression was linked to patient prognosis, we intended to develop a nomogram to predict prognosis based on cuproprosis-related genes characteristics and evaluate its prediction performance.
Cuproprosis-related genes were found to be linked with esophageal cancer prognosis using univariate COX regression analysis on 151 esophageal cancer samples. The C-index, calibration curve, and receiver operator characteristic (ROC) curve were used to evaluate the prediction ability of a prognostic nomogram created by combining clinicopathological variables and cuproprosis-related genes.
Univariate COX regression analysis of 19 Cuproprosis-related genes revealed that the expression of pyruvate dehydrogenase A1 (PDHA1) was associated with the prognosis of esophageal cancer. The low PDHA1 expression group had a better prognosis of esophageal cancer, according to the log-rank test. There was no statistical correlation between PDHA1 expression and 22 immune cells; however there was a correlation between PDHA1 expression and several immune checkpoint genes. The C-index, calibration curve, and ROC curve were used to confirm the predictive ability of the esophageal cancer prognostic nomogram, which was developed by combining pathological type, tumor-node-metastasis stage, and PDHA1 expression.
Cuproprosis-related genes are correlated to esophageal cancer prognosis, and a deep understanding of its molecular mechanism might contribute to novel cancer treatments in the future.
To enhance the overall survival of esophageal cancer patients, researchers must investigate cuproprosis biomarkers and anticipate possible therapy targets.