Identification of microRNA-135b in Stool as a Potential Noninvasive Biomarker for Colorectal Cancer and Adenoma

被引:114
|
作者
Wu, Chung Wah [1 ,2 ,5 ]
Ng, Siew Chien [1 ,2 ]
Dong, Yujuan [1 ,2 ,3 ]
Tian, Linwei [4 ]
Ng, Simon Siu Man [3 ]
Leung, Wing Wa [3 ]
Law, Wai Tak [1 ,2 ]
Yau, Tung On [1 ,2 ,5 ]
Chan, Francis Ka Leung [1 ,2 ]
Sung, Joseph Jao Yiu [1 ,2 ]
Yu, Jun [1 ,2 ,5 ]
机构
[1] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Inst Digest Dis, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Dept Med & Therapeut, State Key Lab Digest Dis, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Dept Surg, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Stanley Ho Ctr Emerging Infect Dis, Hong Kong, Hong Kong, Peoples R China
[5] CUHK Shenzhen Res Inst, Gastrointestinal Canc Biol & Therapeut Lab, Shenzhen, Peoples R China
关键词
FECAL OCCULT BLOOD; HUMAN COLON-CANCER; CT COLONOGRAPHY; EXPRESSION; COLONOSCOPY; DNA; MIR-21;
D O I
10.1158/1078-0432.CCR-13-1750
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Detecting microRNA (miRNA) in stool is a novel approach for colorectal cancer (CRC) screening. This study aimed to identify stool-based miRNA as noninvasive biomarkers for detection of CRC and adenoma. Experimental Design: A miRNA expression array covering 667 human miRNAs was performed on five pairs of CRC and two pairs of advanced adenoma tissues. The most upregulated miRNAs were validated in 40 pairs of CRC tissues, 16 pairs of advanced adenoma tissues, and 424 stool samples, including 104 CRCs, 169 adenomas, 42 inflammatory bowel diseases (IBD), and 109 healthy controls. miRNA levels were followed-up after removal of lesions. Results: In an array analysis, miR-31 and miR-135b were the most upregulated miRNAs in CRC and advanced adenoma as compared with their adjacent normal tissues (>13-fold increase). In stool samples, level of miR-135b was significantly higher in subjects with CRC (P < 0.0001) or adenomas (P < 0.0001), but not in patients with IBD compared with controls. miR-135b showed a significant increasing trend across the adenoma to cancer sequence (P < 0.0001). Levels of miR-31 were not significantly different among groups. The sensitivity of stool mR-135b was 78% for CRC, 73% for advanced adenoma, and 65% for any adenoma, respectively, with a specificity of 68%. No significant difference in the miR-135b level was found between proximal and distal colorectal lesions. Stool miR-135b dropped significantly upon removal of CRC or advanced adenoma (P < 0.0001). Conclusion: Stool-based miR-135b can be used as a noninvasive biomarker for the detection of CRC and advanced adenoma.(C) 2014 AACR.
引用
收藏
页码:2994 / 3002
页数:9
相关论文
共 50 条
  • [1] MicroRNA-135b is associated with tumor progression in colorectal cancer
    Kan, Shi-Feng
    Yang, Jun-Sheng
    Sun, Guan-Xin
    Sun, Jin-Jun
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2016, 9 (03): : 6533 - 6538
  • [2] Detection of MicroRNA-135b in Stool of Patients With Advanced Neoplasm: A Potential Non-Invasive Screening Biomarker?
    Ng, Siew C.
    Law, Wai Tak W.
    Wu, Chung-Wah
    Suen, Bing-Yee
    Lau, James Y.
    Chan, Francis K. L.
    Sung, Joseph J.
    Yu, Jun
    GASTROENTEROLOGY, 2012, 142 (05) : S32 - S33
  • [3] MicroRNA-135b and its circuitry networks as potential therapeutic targets in colon cancer
    Khatri, Rohini
    Subramanian, Subbaya
    FRONTIERS IN ONCOLOGY, 2013, 3
  • [4] Targeting microRNA-135b in cardiac hypertrophy
    Tian, Bing
    Liu, Jingwen
    Tang, Lina
    INTERNATIONAL JOURNAL OF CARDIOLOGY, 2021, 329 : 176 - 176
  • [5] MicroRNA-135b regulates metastasis suppressor 1 expression and promotes migration and invasion in colorectal cancer
    Wu, Weiyun
    Wang, Zhuang
    Yang, Pengchun
    Yang, Jingfang
    Liang, Jian
    Chen, Yuanhong
    Wang, Hao
    Wei, Guoli
    Ye, Shicai
    Zhou, Yu
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2014, 388 (1-2) : 249 - 259
  • [6] MicroRNA-135b regulates metastasis suppressor 1 expression and promotes migration and invasion in colorectal cancer
    Weiyun Wu
    Zhuang Wang
    Pengchun Yang
    Jingfang Yang
    Jian Liang
    Yuanhong Chen
    Hao Wang
    Guoli Wei
    Shicai Ye
    Yu Zhou
    Molecular and Cellular Biochemistry, 2014, 388 : 249 - 259
  • [7] MicroRNA-135b regulates apoptosis and chemoresistance in colorectal cancer by targeting large tumor suppressor kinase 2
    He, Yuqi
    Wang, Jianxun
    Wang, Jiheng
    Yung, Victoria Yee-Wa
    Hsu, Emily
    Li, Aiqin
    Kang, Qian
    Ma, Junbiao
    Han, Qingfeng
    Jin, Peng
    Xing, Rui
    Lu, Youyong
    Sheng, Jianqiu
    AMERICAN JOURNAL OF CANCER RESEARCH, 2015, 5 (04): : 1382 - 1395
  • [8] STAT3 UPREGULATES EXPRESSION OF MICRORNA-135B IN COLON CANCER
    Khatri, R.
    Subramanian, S.
    DISEASES OF THE COLON & RECTUM, 2014, 57 (05) : E298 - E299
  • [9] microRNA-135b promotes cancer progression acting as a downstream effector of oncogenic pathways in colon cancer
    Valeri, Nicola
    Braconi, Chiara
    Gasparini, Pierluigi
    Hart, Jonathan
    Grivennikov, Sergei
    Lovat, Francesca
    Lanza, Giovanni
    Gafa, Roberta
    Nuovo, Gerard
    Frankel, Wendy
    Groden, Joanna
    Vogt, Peter K.
    Karin, Michael
    Croce, Carlo M.
    LANCET, 2013, 381 : 17 - 17
  • [10] MicroRNA-135b Promotes Cancer Progression by Acting as a Downstream Effector of Oncogenic Pathways in Colon Cancer
    Valeri, Nicola
    Braconi, Chiara
    Gasparini, Pierluigi
    Murgia, Claudio
    Lampis, Andrea
    Paulus-Hock, Viola
    Hart, Jonathan R.
    Ueno, Lynn
    Grivennikov, Sergei I.
    Lovat, Francesca
    Paone, Alessio
    Cascione, Luciano
    Sumani, Khlea M.
    Veronese, Angelo
    Fabbri, Muller
    Carasi, Stefania
    Alder, Hansjuerg
    Lanza, Giovanni
    Gafa', Roberta
    Moyer, Mary P.
    Ridgway, Rachel A.
    Cordero, Julia
    Nuovo, Gerard J.
    Frankel, Wendy L.
    Rugge, Massimo
    Fassan, Matteo
    Groden, Joanna
    Vogt, Peter K.
    Karin, Michael
    Sansom, Owen J.
    Croce, Carlo M.
    CANCER CELL, 2014, 25 (04) : 469 - 483