Identifying the Trends of Urinary microRNAs within Extracellular Vesicles for Esophageal Cancer

被引:1
作者
Hisaoka, Kazuhiko [1 ]
Matsuda, Satoru [1 ]
Minoura, Kodai [2 ]
Yamaguchi, Hiroki [2 ]
Ichikawa, Yuki [2 ]
Mizunuma, Mika [2 ]
Kobayashi, Ryota [1 ]
Morimoto, Yosuke [1 ]
Takeuchi, Masashi [1 ]
Fukuda, Kazumasa [1 ]
Nakamura, Rieko [1 ]
Hori, Shutaro [1 ]
Yamazaki, Taigi [3 ]
Sambe, Takehiko [4 ]
Kawakubo, Hirofumi [1 ]
Kitagawa, Yuko [1 ]
机构
[1] Keio Univ, Sch Med, Dept Surg, 35 Shinanomachi,Shinjuku Ku, Tokyo 1608582, Japan
[2] Craif Inc, Tokyo 1130034, Japan
[3] Showa Univ, Grad Sch Pharm, Dept Clin Res & Dev, Tokyo 1428555, Japan
[4] Showa Univ, Grad Sch Med, Dept Clin Pharmacol, Tokyo 1428555, Japan
关键词
urinary microRNAs; esophageal squamous cell carcinoma; liquid biopsy; biomarkers; SQUAMOUS-CELL CARCINOMA; CHEMORADIOTHERAPY;
D O I
10.3390/cancers16091698
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary The advancement of multidisciplinary treatment has increased the need to develop a test to monitor tumor burden during treatment. We herein analyzed urinary microRNAs within extracellular vesicles from patients with esophageal squamous cell carcinoma (ESCC) and normal individuals using a microarray, and identified 18 microRNAs which were significantly expressed in ESCC patients.Abstract Background: The advancement of multidisciplinary treatment has increased the need to develop tests to monitor tumor burden during treatment. We herein analyzed urinary microRNAs within extracellular vesicles from patients with esophageal squamous cell carcinoma (ESCC) and normal individuals using a microarray. Methods: Patients with advanced ESCC who underwent esophagectomy (A), endoscopic submucosal resection (ESD) (B), and healthy donors (C) were included. Based on microRNA expression among the groups (Analysis 1), microRNAs with significant differences between groups A and C were selected (Analysis 2). Of these candidates, microRNAs in which the change between A and C was consistent with the change between B and C were selected for downstream analysis (Analysis 3). Finally, microRNA expression was validated in patients with recurrence from A (exploratory analysis). Results: For analysis 1, 205 microRNAs were selected. For Analyses 2 and 3, the changes in 18 microRNAs were consistent with changes in tumor burden as determined by clinical imaging and pathological findings. The AUC for the detection of ESCC using 18 microRNAs was 0.72. In exploratory analysis, three of eighteen microRNAs exhibited a concordant trend with recurrence. Conclusions: The current study identified the urinary microRNAs which were significantly expressed in ESCC patients. Validation study is warranted to evaluate whether these microRNAs could reflect tumor burden during multidisciplinary treatment for ESCC.
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页数:10
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