4.5 Article

Serum Exosomal miRNA-1226 as Potential Biomarker of Pancreatic Ductal Adenocarcinoma

Journal

ONCOTARGETS AND THERAPY
Volume 14, Issue -, Pages 1441-1451

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/OTT.S296816

Keywords

exosome; miRNA; pancreatic ductal adenocarcinoma; miRNA-1226-3p

Funding

  1. National Natural Science Foundation of China [81771899, 81773460]
  2. Key Program of Research and Development of Jiangsu Province [BE2017772]
  3. Jiangsu Provincial Hospital of Chinese Medicine Peak Academic Talent Project [y2018rc04]
  4. Jiangsu Provincial Traditional Chinese Medicine Science and Technology Development Plan [ZD201907]

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The study identified miRNA-1226-3p as a potential biomarker for detecting PDAC and predicting tumor invasion or metastases. Experimental results demonstrated that miRNA-1226-3p can inhibit proliferation, promote apoptosis, and suppress migration of PDAC cells.
Background: Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer-related mortality and it is urgent to find biomarkers for early detection of PDAC. Exosomal miRNAs are useful biomarkers for cancer detection. The aims of this study were to investigate the potential role of serum exosomal miRNA in detection of PDAC and to analyze the correlation between the levels of exosome miRNA and the tumor biological behaviors. Materials and Methods: Thirteen serum samples were collected from five patients with PDACs, three healthy individuals (HIs) and five benign pancreatic lesions (BP) for a high throughput profiling analysis to identify an altered miRNA expression patterns in PDAC. Candidate exosomal miRNAs were filtered based on a second independent cohort that included 17 PDACs and 12 benign pancreatic lesions by quantitative real-time polymerase chain reaction (qRT-PCR). Four miRNAs were selected for miRNA validation as PDAC biomarkers in a subsequent set of samples. The association between candidate exosomal miRNA and tumor behavior (tumor invasion or metastases) was evaluated in 17 PDACs. In vitro studies were performed to evaluate the role of candidate exosomal miRNA on cell viability, apoptosis and cell migration in two PDAC cell lines. Results: The expression of 11 miRNAs showed same trend between PDAC and BP, and between PDAC and His. Six of them were upregulated (miR-203b-5p, miR-342-5p, miR-337-5p, miR-149-5p, miR-877-5p, miR-203a-3p), and five were downregulated (miR-1226-3p, miR-3182, miR-625-3p, miR-624-5p, miR-664a-5p). miR-1226-3p was selected as the candidate exosomal biomarker for the PDAC detection. The expression of serum exosomal miRNA-1226-3p was downregulated in PDACs compared to the BPs (p = 0.025). miR-1226-3p had acceptable performance in predicting [area under the curve (AUC) = 0.74] PDAC. Exosomal miRNA-1226-3p level in PDAC with invasion or metastases was lower than that without invasion or metastases (p = 0.028). Transfection of miRNA-1226-3p significantly inhibited the proliferation of PANC-1 and BXP-3 cells, stimulated cell apoptosis and inhibited cell migration. Conclusion: Serum exosomal miRNA-1226-3p is a potential biomarker in diagnosing and predicting the tumor invasion or metastases of PDAC.

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