Development of a prognostic prediction model based on microRNA-1269a in esophageal cancer

被引:4
作者
Yu, Yong [1 ]
Ren, Kai-Ming [2 ]
机构
[1] China Med Univ, Dept Ophtalmol, Shengjing Hosp, Shenyang 110004, Liaoning, Peoples R China
[2] China Med Univ, Dept Thorac Surg, Shengjing Hosp, 36 Sanhao St, Shenyang 110004, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNA-1269a; Esophageal cancer; Prognosis; Overall survival; Cancer-specific survival; HEPATOCELLULAR-CARCINOMA; PROMOTES PROLIFERATION; NONCODING RNA; PREVENTION; BIOMARKERS; DIAGNOSIS; EDITION; EUS;
D O I
10.4251/wjgo.v13.i8.943
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND Esophageal cancer (ESCA) is a heterogeneous cancer with variable outcomes that are challenging to predict. MicroRNA (miR)-1269a is a newly discovered non-coding RNA that shows promising prognostic prediction in other cancers, but its clinical value in ESCA remains unclear. AIM To explore the relationship between miR-1269a and its clinical value and to develop a nomogram to succinctly display this relationship. METHODS We analyzed the expression of miR-1269a in 125 ESCA tissue samples with complete clinical data and 52 normal tissue samples. We determined the prognostic value of miR-1269a for overall survival (OS) and cancer-specific survival (CSS) and evaluated the association between miR-1269a and clinical variables including tumor location, histologic grade, metastatic stage, and American Joint Committee on Cancer (AJCC) stage using multivariate Cox analysis. Additionally, we developed a nomogram for OS and CSS based on miR-1269a expression using age and AJCC stage and assessed its prognostic performance. Using Gene Ontology and Kyoto Encyclopedia of Gene and Genomes analyses, we predicted the target genes of miR-1269a and analyzed their potential function in caner development. RESULTS The expression of miR-1269a was significantly higher in ESCA patients than healthy controls. Patients with high expression of miR-1269a showed poor prognosis in OS and CSS, suffered increased rates of low differentiation and metastasis, and exhibited tumor stage T3 + T4, positive lymph stage, and AJCC stage III + IV. The area under the receiver operating characteristic curve of miR-1269a was 0.716 for OS and 0.764 for CSS. Multivariate Cox analysis revealed that AJCC stage and miR-1269a were independent factors for OS and CSS. Combing with age, we constructed a nomogram for prognostic prediction. Additionally, our nomogram showed excellent predictive performance for OS and CSS after 3 years and 5 years and was easy to use. Ultimately, the functional analysis suggested that miR-1269a was mostly involved in the PI3K-AKT signaling pathway. CONCLUSION miR-1269a can be used as a potential indicator for the prognosis of ESCA patients. We developed an easy-to-use nomogram with excellent ESCA prognostic prediction for clinical use.
引用
收藏
页码:943 / 958
页数:16
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