Serum miR-1301-3p, miR-335-5p, miR-28-5p, and their target B7-H3 may serve as novel biomarkers for colorectal cancer

被引:4
|
作者
Wang, Lei [1 ]
Zhao, Yajuan [2 ]
Xu, Minyi [1 ]
Zhou, Fangfang [1 ]
Yan, Ji [2 ]
机构
[1] Shanghai Sixth Peoples Hosp, Xuhui Branch, Shanghai Peoples Hosp 8, Dept Clin Lab, 8 Caobao Rd, Shanghai 200235, Peoples R China
[2] Shanghai Sixth Peoples Hosp, Xuhui Branch, Shanghai Peoples Hosp 8, Dept Pathol, Shanghai 200235, Peoples R China
来源
JOURNAL OF BUON | 2019年 / 24卷 / 03期
关键词
colorectal cancer; B7-H3; biomarker; microRNA; LIVER METASTASES; EXPRESSION; DIAGNOSIS; CA125; IDENTIFICATION; ASSOCIATION; MICRORNA; CA72-4; CA199; CEA;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: B7-H3, a member of the B7 family of immune regulatory ligands, plays a critical role in the T cell-mediated immune response. It is broadly expressed in several human cancers and leads to poor prognosis. Nevertheless, the clinical significance of B7-H3 expression in colorectal cancer (CRC) remains unclear. Methods: The serum B7-H3,137-H1, cancer-associated carbohydrate antigen-50 (CA-50) and carcinoembryonic antigen (CEA) expressions in patients with CRC, benign gastrointestinal diseases, and healthy controls were measured by ELISA. The miRNAs that target B7-H3 were predicted by using the miRTarBase. Real-time PCR was performed to examine their expressions in patients with CRC. Results: B7-H3, B7-H1, and CA-50 expressions were higher in patients with CRC than those in healthy controls and the patients with benign gastrointestinal diseases. B7-H3 expression was correlated with TNM stage and metastasis. It was predicted that B7-H3 was a target of miR-1301-3p, miR-335-5p, and miR-28-5p and its expression was negatively related to these three miRNAs expressions. Serum miR1301-3p, miR-335-5p, and miR-28-5p expressions were also correlated with the TNM stage and metastasis. Conclusion: Our results indicated that serum miR-1301-3p, miR-28-5p, miR-335-5p, and B7-H3 expressions were correlated with pathological stages of CRC and metastasis and may therefore serve as novel biomarkers for CRC diagnosis and treatment.
引用
收藏
页码:1120 / 1127
页数:8
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