Circular RNA ciRS-7-A Promising Prognostic Biomarker and a Potential Therapeutic Target in Colorectal Cancer

被引:455
|
作者
Weng, Wenhao [1 ,2 ,3 ]
Wei, Qing [4 ]
Toden, Shusuke [1 ,2 ]
Yoshida, Kazuhiro [1 ,2 ]
Nagasaka, Takeshi [5 ]
Fujiwara, Toshiyoshi [5 ]
Cai, Sanjun [6 ,7 ]
Qin, Huanlong [8 ]
Ma, Yanlei [6 ,7 ]
Goel, Ajay [1 ,2 ]
机构
[1] Baylor Univ, Med Ctr, Ctr Gastrointestinal Res, 3410 Worth St,Suite 610, Dallas, TX 75246 USA
[2] Baylor Univ, Med Ctr, Ctr Translat Genom & Oncol, Baylor Scott & White Res Inst,Charles A Sammons C, 3410 Worth St,Suite 610, Dallas, TX 75246 USA
[3] Tongji Univ, Shanghai Peoples Hosp 10, Dept Clin Lab, Shanghai, Peoples R China
[4] Tongji Univ, Shanghai Peoples Hosp 10, Dept Pathol, Shanghai, Peoples R China
[5] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Gastroenterol Surg & Surg Oncol, Okayama, Japan
[6] Fudan Univ, Shanghai Canc Ctr, Dept Colorectal Surg, Shanghai, Peoples R China
[7] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai, Peoples R China
[8] Tongji Univ, Shanghai Peoples Hosp 10, Dept Gastrointestinal Surg, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
STEM-LIKE CELLS; TUMOR-SUPPRESSOR; LUNG-CANCER; MICRORNA-7; GROWTH; EXPRESSION; RECEPTOR; MIR-7; PROLIFERATION; MECHANISMS;
D O I
10.1158/1078-0432.CCR-16-2541
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Colorectal cancer is one of themost common malignancies worldwide. Recently, a novel circular RNA, ciRS-7, was proposed to be a potential miR-7 sponge. As miR-7, a putative tumor-suppressor, regulates the expression of several important drivers of colorectal cancer, we analyzed the clinical significance of ciRS-7 in colorectal cancer patients. Experimental Design: Initially, we evaluated the expression levels of ciRS-7 in a training cohort comprising of 153 primary colorectal cancer tissues and 44 matched normal mucosae. We subsequently confirmed its clinical relevance in an independent validation cohort (n = 165), and evaluated the effect of ciRS-7 on miR-7, and its target genes EGFR and RAF1. Functional analyses were performed in cell lines and an animal model to support clinical findings. Results: Our data revealed that ciRS-7 was significantly upregulated in colorectal cancer tissues compared with matched normal mucosae (P = 0.0018), and its overexpression was associated with poor patient survival (P = 0.0224 and 0.0061 in the training and validation cohorts, respectively). Multivariate survival analysis revealed that ciRS-7 emerged as an independent risk factor for overall survival (P = 0.0656 and 0.0324 in the training and validation cohorts, respectively). Overexpression of ciRS-7 in HCT116 and HT29 cells led to the blocking of miR-7 and resulted in a more aggressive oncogenic phenotype, and ciRS-7 overexpression permitted the inhibition of miR-7 and subsequent activation of EGFR and RAF1 oncogenes. Conclusions: CiRS-7 is a promising prognostic biomarker in colorectal cancer patients and may serve as a therapeutic target for reducing EGFR-RAF1 activity in colorectal cancer patients. (C) 2017 AACR.
引用
收藏
页码:3918 / 3928
页数:11
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