A Novel Ferroptosis-Related Gene Signature Predicts Overall Survival of Breast Cancer Patients.
A Novel Ferroptosis-Related Gene Signature Predicts Overall Survival of Breast Cancer Patients.
复制标题
一种新的铁死亡相关基因特征可预测乳腺癌患者的总体生存率
DOI:
10.3390/biology10020151
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发表时间:
2021-02-14
期刊:
影响因子:
4.2
通讯作者:
Shi Y
中科院分区:
文献类型:
--
作者:
Li H;Li L;Xue C;Huang R;Hu A;An X;Shi Y
Simple Summary Ferroptosis is an iron-dependent cell death which is distinctive from common forms of cell death. Accumulating evidence indicated the close relationship between ferroptosis and numerous human diseases. Regarding breast cancer, a related study indicated that some targeted medicines could induce ferroptosis, furthermore, some basic research found that ferroptosis-related genes were closely related to breast cancer. However, the correlation between ferroptosis-related genes and breast cancer patients’ prognosis remains unknown. We built an 8-ferroptosis-related-gene model to predict breast cancer patients’ prognosis. This model could stratify patients into high- or low-risk groups. Additionally, tumor microenvironment analyses displayed differently enriched immune cells and immune pathways between these two groups. This 8-gene model is believed to be of great value in predicting prognosis for breast cancer patients. Abstract Breast cancer is the second leading cause of death in women, thus a reliable prognostic model for overall survival (OS) in breast cancer is needed to improve treatment and care. Ferroptosis is an iron-dependent cell death. It is already known that siramesine and lapatinib could induce ferroptosis in breast cancer cells, and some ferroptosis-related genes were closely related with the outcomes of treatments regarding breast cancer. The relationship between these genes and the prognosis of OS remains unclear. The data of gene expression and related clinical information was downloaded from public databases. Based on the TCGA-BRCA cohort, an 8-gene prediction model was established with the least absolute shrinkage and selection operator (LASSO) cox regression, and this model was validated in patients from the METABRIC cohort. Based on the median risk score obtained from the 8-gene model, patients were stratified into high- or low-risk groups. Cox regression analyses identified that the risk score was an independent predictor for OS. The findings from CIBERSORT and ssGSEA presented noticeable differences in enrichment scores for immune cells and pathways between the abovementioned two risk groups. To sum up, this prediction model has potential to be widely applied in future clinical settings.
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影响因子:
14.8
作者:
Doll S;Proneth B;Tyurina YY;Panzilius E;Kobayashi S;Ingold I;Irmler M;Beckers J;Aichler M;Walch A;Prokisch H;Trümbach D;Mao G;Qu F;Bayir H;Füllekrug J;Scheel CH;Wurst W;Schick JA;Kagan VE;Angeli JP;Conrad M
通讯作者:
Conrad M
影响因子:
4.4
作者:
Martinez, Fernando O.;Gordon, Siamon;Mantovani, Alberto
通讯作者:
Mantovani, Alberto
影响因子:
5.5
作者:
Liu, Han-jie;Hu, Hui-min;Jiang, Tao
通讯作者:
Jiang, Tao
影响因子:
0.7
作者:
Nucera, Silvia;Biziato, Daniela;De Palma, Michele
通讯作者:
De Palma, Michele
影响因子:
64.8
作者:
Jiang, Le;Kon, Ning;Li, Tongyuan;Wang, Shang-Jui;Su, Tao;Hibshoosh, Hanina;Baer, Richard;Gu, Wei
通讯作者:
Gu, Wei