4.7 Article

Circulating MicroRNAs in Small-bowel Neuroendocrine Tumors A Potential Tool for Diagnosis and Assessment of Effectiveness of Surgical Resection

期刊

ANNALS OF SURGERY
卷 274, 期 1, 页码 E1-E9

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/SLA.0000000000003502

关键词

biomarkers; microRNAs; neuroendocrine tumor; recurrent disease; serum; small bowel

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资金

  1. Cancer Research UK Imperial Centre
  2. Action Against Cancer
  3. Dr HeinzHorst Deichmann Foundation
  4. National Institute for Health Research (NIHR) Biomedical Research Centre at Imperial College Healthcare NHS Trust and Imperial College London
  5. European Neuroendocrine Tumor Society (ENETS)
  6. Cancer Research UK (CRUK)

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This study identified four serum miRNAs that were significantly up-regulated in SBNET, with miR-125b-5p and miR-362-5p showing potential to detect residual and recurrent disease. The longitudinal assessment revealed changes in miRNA expression after surgical resection, providing insights into disease progression and monitoring.
Objective: To discover serum-based microRNA (miRNA) biomarkers for small-bowel neuroendocrine tumors (SBNET) to help guide clinical decisions. Background: MiRNAs are small noncoding RNA molecules implicated in the initiation and progression of many cancers. MiRNAs are remarkably stable in bodily fluids, and can potentially be translated into clinically useful biomarkers. Novel biomarkers are needed in SBNET to determine disease aggressiveness, select patients for treatment, detect early recurrence, and monitor response. Methods: This study was performed in 3 stages (discovery, validation, and a prospective, longitudinal assessment). Discovery comprised of global profiling of 376 miRNA in sera from SBNET patients (n = 11) versus healthy controls (HCs; n = 3). Up-regulated miRNAs were subsequently validated in additional SBNET (n = 33) and HC sera (n = 14); and then longitudinally after SBNET resection (n = 12), with serial serum sampling (preoperatively day 0; postoperatively at 1 week, 1 month, and 12 months). Results: Four serum miRNAs (miR-125b-5p, -362- 5p, -425- 5p and -500a5p) were significantly up-regulated in SBNET (P < 0.05; fold-change >2) based on multiple normalization strategies, and were validated by RT-qPCR. This combination was able to differentiate SBNET from HC with an area under the curve of 0.951. Longitudinal assessment revealed that miR-125b-5p returned towards HC levels at 1 month postoperatively in patients without disease, whereas remaining up-regulated in those with residual disease (RSD). This was also true at 12 months postoperatively. In addition, miR-362-5p appeared up-regulated at 12 months in RSD and recurrent disease (RCD). Conclusions: Our study represents the largest global profiling of serum miRNAs in SBNET patients, and the first to evaluate ongoing serum miRNA expression changes after surgical resection. Serum miR-125b-5p and miR362-5p have potential to be used to detect RSD/RCD.

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