Development and Validation of a Novel Metabolic Signature-Based Prognostic Model for Uveal Melanoma.
Development and Validation of a Novel Metabolic Signature-Based Prognostic Model for Uveal Melanoma.
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基于代谢特征的新型葡萄膜黑色素瘤预后模型的开发和验证
DOI:
10.1167/tvst.11.5.9
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发表时间:
2022-05-02
影响因子:
3
通讯作者:
Sun, Xiaodong
中科院分区:
文献类型:
--
作者:
Shi, Ke;Li, Xinxin;Zhang, Jingfa;Sun, Xiaodong
Uveal melanoma (UM) is the most common primary malignant tumor with poor prognosis. The role of metabolism-related genes in the prognosis of UM remains unrevealed. This study aimed to establish and validate a prognostic prediction model for UM based on metabolism-related genes. Gene expression profiles and clinicopathological information were downloaded from The Cancer Genome Atlas, and the Gene Expression Omnibus database. Univariable Cox regression, least absolute shrinkage and selection operator Cox regression, and stepwise regression were performed to establish the model. Kaplan-Meier survival analysis, receiver operating characteristic (ROC) curve analysis, and calibration and discrimination analyses were used to evaluate the prognostic model. Three metabolism-related genes, carbonic anhydrase 12, acyl-CoA synthetase long-chain family member 3, and synaptojanin 2, and three clinicopathological parameters (i.e., age, gender, and metastasis staging) were identified to establish the model. The risk score was found to be an independent prognostic factor for UM survival. High-risk patients demonstrated significantly poorer prognosis than low-risk patients. ROC analysis suggested the promising prognostic efficiency of the model. The calibration curve manifested satisfactory agreement between the predicted and observed risk. A nomogram and online survival calculator were developed to predict the survival probability. The novel metabolism-based prognostic model could accurately predict the prognosis of UM patients, which facilitates the prediction of the survival probability by both ophthalmologists and patients with the online dynamic nomogram. The dynamic nomogram links gene expression profiles to clinical prognosis of UM and is useful to evaluate the survival probability.
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影响因子:
6.6
作者:
Fernández LP;Merino M;Colmenarejo G;Moreno-Rubio J;Sánchez-Martínez R;Quijada-Freire A;Gómez de Cedrón M;Reglero G;Casado E;Sereno M;Ramírez de Molina A
通讯作者:
Ramírez de Molina A
DOI:
10.3390/diagnostics11020219
发表时间:
2021-02-02
期刊:
Diagnostics (Basel, Switzerland)
影响因子:
--
作者:
Luo H;Ma C
通讯作者:
Ma C
影响因子:
--
作者:
Shields, Carol L.;Furuta, Minoru;Shields, Jerry A.
通讯作者:
Shields, Jerry A.
影响因子:
45.3
作者:
Rietschel, P;Panageas, KS;Chapman, PB
通讯作者:
Chapman, PB
影响因子:
21.3
作者:
Boroughs LK;DeBerardinis RJ
通讯作者:
DeBerardinis RJ