4.3 Article

Low plasma levels of miR-101 are associated with tumor progression in gastric cancer

Journal

ONCOTARGET
Volume 8, Issue 63, Pages 106538-106550

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.20860

Keywords

gastric cancer; tumor suppressor microRNA; plasma; biomarker

Funding

  1. JSPS KAKENHI [15K10112]
  2. Grants-in-Aid for Scientific Research [15K10112] Funding Source: KAKEN

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Background: Several studies have identified the decreased expression of the tumor suppressor miR-101 in various cancers. In this study, we tested miR-101 as a potential therapeutic target and novel plasma biomarker for gastric cancer (GC). Results: The miR-101 expression level was significantly lower in GC tissues (P = 0.0038) and GC cell lines (P = 0.0238) than in normal gastric mucosa. Both exosomal and plasma miR-101 were significantly downregulated in GC patients compared with healthy volunteers (P = 0.0281 and P < 0.0001, respectively). Low miR-101 plasma level was significantly associated with advanced T factor, advanced disease stage, and peritoneal metastasis and predicted poor prognosis in GC patients (P = 0.0368; hazard ratio, 3.079; 95% confidence interval: 1.06-11.08). Overexpression of miR-101 in GC cells induced apoptosis by inhibiting MCL1 and suppressed cell migration and invasion by regulating ZEB1. Conclusions: Depletion of the tumor suppressor miRNA-101 in plasma is related to tumor progression and poor outcomes. Low plasma miR-101 may be a biomarker for GC, and its restoration might be a novel anticancer treatment strategy.

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