Long non-coding RNAs LOC285194, RP11-462C24.1 and Nbla12061 in serum provide a new approach for distinguishing patients with colorectal cancer from healthy controls

被引:34
作者
Wang, Chuanxi [1 ]
Yu, Jinyu [1 ]
Han, Yuping [2 ]
Li, Leping [3 ]
Li, Jie [4 ]
Li, Tao [4 ]
Qi, Peng [5 ,6 ,7 ]
机构
[1] Shandong Univ, Shandong Prov Hosp, Dept Oncol, Jinan, Shandong, Peoples R China
[2] Shandong Univ, Shandong Prov Hosp, Dept Emergency, Jinan, Shandong, Peoples R China
[3] Shandong Univ, Shandong Prov Hosp, Dept Gastrointestinal Surg, Jinan, Shandong, Peoples R China
[4] Shandong Univ, Shandong Prov Hosp, Dept Infect Dis, Jinan, Shandong, Peoples R China
[5] Fudan Univ, Dept Pathol, Shanghai Canc Ctr, Shanghai, Peoples R China
[6] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai, Peoples R China
[7] Fudan Univ, Inst Pathol, Shanghai, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
long non-coding RNA; serum; colorectal cancer; biomarker; POOR-PROGNOSIS; LOW EXPRESSION; CLINICAL-SIGNIFICANCE; BIOMARKERS; LNCRNA; DIAGNOSIS; MICRORNAS; PLASMA;
D O I
10.18632/oncotarget.12220
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) is currently the most prevalent malignant cancer worldwide. However, there is a lack of efficient biomarkers for CRC screening. Accumulating evidence reveals that long non-coding RNAs (lncRNAs) detectable in serum are associated with the genesis and development of various types of cancer. Therefore, we examined the diagnostic ability of lncRNAs in blood samples from patients with CRC by evaluating the levels of 17 CRC- or gastrointestinal cancer-related lncRNAs in serum samples from 71 CRC patients and 70 healthy individuals using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). We detected 13 lncRNAs in serum, three of which displayed significantly different levels between CRC patients and healthy controls. A three-lncRNA signature (LOC285194, RP11462C24.1 and Nbla12061) identified via stepwise regression analysis showed potential as a diagnostic marker for CRC. The area under the receiver operating characteristic curve of this signature for distinguishing CRC patients from healthy individuals was 0.793 (95% CI: 0.709 to 0.861). The diagnostic ability of this marker was much higher than that of conventional blood biomarkers such as carcinoembryonic antigen (CEA), carbohydrate antigen 199 (CA199), carbohydrate antigen 125 (CA125) and carbohydrate antigen 724 (CA724). Combining this novel marker with conventional biomarkers produced even greater diagnostic ability. Furthermore, the levels of the three lncRNAs decreased after the patients underwent surgical resection. The results of this study suggest an additional marker for CRC screening and provide new directions for further investigation.
引用
收藏
页码:70769 / 70778
页数:10
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