4.6 Article

Exosomal miR-590-5p in Serum as a Biomarker for the Diagnosis and Prognosis of Gastric Cancer

Journal

FRONTIERS IN MOLECULAR BIOSCIENCES
Volume 8, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmolb.2021.636566

Keywords

exosome; miRNA-590-5p; gastric cancer; serum; biomarker

Funding

  1. National Natural Science Foundation [81573953, 81703753, 81973634, 81603340]
  2. Natural Science Foundation of Zhejiang Province [LY18H290006]
  3. Program of Zhejiang Provincial TCM Sci-tech Plan [2016ZZ012, 2018ZB044, 2018ZY006]
  4. Zhejiang Provincial Science and Technology Projects [2018C37045]
  5. Research Fund of Zhejiang Chinese Medicine University [2018ZY09]
  6. Zhejiang Medicine and Health Projects [2020365132]
  7. Medical Health Science and Technology Project of Zhejiang Provincial Health Commission [2017PY009]
  8. Zhejiang Provincial Research Center for Upper Gastrointestinal Tract Cancer [JBZX-202006]

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The study found that the expression of exosomal miR-590-5p is associated with the clinical stage, infiltration depth, and ki-67 expression level of GC. A decrease in exosomal miR-590-5p expression is correlated with a decrease in overall survival rate. As an independent predictor, miR-590-5p may inhibit cell migration and invasion, potentially serving as a biomarker for early detection and prediction of GC.
The purpose of this study is to explore the expression of miRNA-590-5p, an exosome of gastric cancer (GC), and to evaluate the suitability of miR-590-5p, an exosome with its own clinical characteristics. Serum samples from 168 gastric cancer patients and 50 matched controls were collected and exosomal RNAs were extracted. After that, miR-590-5p is analyzed by quantitative polymerase chain reaction (qRT-PCR), which is more related to clinical and pathological parameters and patient monitoring data. MGC-803 and HGC-27 cells were treated by miR-590-5p mimics, and then the changes of cell fluidity and invasiveness were monitored. The results showed that the expression level of miR-590-5p in exosomes of healthy observation group, early (I and II) stage group, and late stage (III) group was 30.34 +/- 6.35, 6.19 +/- 0.81, and 2.9 +/- 0.19, respectively (all p < 0.05). ROC (receiver-operating characteristic curve) showed that the AUC (area under the curve) of exosomal miR-590-5p was 0.810 with 63.7% sensitivity and 86% specificity. The expression of exosomal miR-590-5p in serum was related to clinical stage (p = 0.008), infiltration depth, and the expression level of ki-67 (p < 0.001). In addition, Kaplan-Meier analysis showed that the decrease of explicit level of exosomal miR-590-5p was related to the decrease of overall survival rate (p < 0.001). Cox regression analysis showed that miR-590-5p can be used as an independent predictor. Furthermore, upregulation of miR-590-5p inhibited cell migration and invasion in MGC-803 cells and HGC-27 cells. The serum expression level of exosomal miR-590-5p may be a biomarker, which is potentially useful and noninvasive for early detection and prediction of GC. In addition, miR-590-5p can play a role in eliminating carcinogens by actively regulating the malignant potential of gastric cancer.

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