Long Non-Coding RNA Signatures Associated with Ferroptosis Predict Prognosis in Colorectal Cancer

被引:31
|
作者
Li, Na [1 ]
Shen, Jiangli [1 ]
Qiao, Ximin [2 ]
Gao, Yuan [3 ]
Su, Hong-Bo [4 ]
Zhang, Shuai [5 ]
机构
[1] Xianyang Cent Hosp, Dept Anorectal Surg, Xianyang, Shaanxi, Peoples R China
[2] Xianyang Cent Hosp, Deans Off, Xianyang, Shaanxi, Peoples R China
[3] Xianyang Cent Hosp, Surg Dept, Xianyang, Shaanxi, Peoples R China
[4] Xian Hosp TCM, Anorectal Hosp, Ward 2, Xian, Shaanxi, Peoples R China
[5] Hebei Univ Chinese Med, Journal Editorial Board, Shijiazhuang, Hebei, Peoples R China
来源
INTERNATIONAL JOURNAL OF GENERAL MEDICINE | 2022年 / 15卷
关键词
colorectal cancer; ferroptosis; lncRNAs; immune infiltration; TCGA; PROMOTES; LNCRNAS;
D O I
10.2147/IJGM.S331378
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Currently, colorectal cancer has become a common gastrointestinal malignancy that usually occurs in the colon and rectum, and ferroptosis plays a vital role in the pathology and progression of colorectal tumors. Methods: A total of 627 patients (51 normal and 644 tumor samples) from The Cancer Genome Atlas (TCGA)-COAD and TCGA-READ were included in the study. Lasso and Cox's regression was employed to analyze the characteristic lncRNAs in colorectal cancer samples, and a distinctive prognostic model of ferroptosis-related lncRNAs was established. By analyzing the divergence between the high and low-risk groups of ferroptosis-related lncRNAs, 15 characteristic lncRNAs related to the prognosis of colorectal cancer were evaluated. Kaplan-Meier analysis, operation characteristic curve (ROC), nomogram, and gene set enrichment analyses (GSEA) further confirmed the validity of the characteristic prognostic model with ferroptosis-related lncRNAs. Results: Kaplan-Meier analysis confirmed a high-risk group of ferroptosis-related lncRNA interrelated with a poor prognosis in colorectal cancer. AUC estimates of 1 -, 3 -, and 5-year survival rates for ferroptosis-related lncRNA characteristic models were 0.745, 0.767 and 0.789. GSEA analysis showed that immune and malignancy-related pathways were active in the high-risk score group. In addition, differential analyses of immune function, including Checkpoint, cytolytic, HLA, and T cell co-inhibition, differed significantly betwixt low - and high-risk groups.CD160, TNFRSF18, CD27, PDCD1, CD200R1, ADORA2A, TNFRSF14, LAIR1, CD244, CD40, TNFRSF4, CD70, TNFSF14, TNFRSF25, CD276, HHLA2, VTCN1, LAGS, TNFSF18, and other immune checkpoints had different expressions betwixt the high- and low-risk group. Conclusion: Fifteen kinds of lncRNAs with different expressions (AP003555.1, AC099850.3, AL031985.3, LINC01857, STPG3-AS1, AL137782.1, AC124067.4, AC012313.5, AC083900.1, AC010973.2, ALMS1-IT1, AC013652.1, AC133540.1, AP006621.2, AC018653.3) were closely associated with poor prognosis of colorectal cancer. These indicators were significantly correlated with the overall survival (OS) rate and could be used as prognostic evaluation criteria.
引用
收藏
页码:33 / 43
页数:11
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