The correlation of circulating pro‐angiogenic mi RNA s’ expressions with disease risk, clinicopathological features, and survival profiles in gastric cancer

This study aimed to explore the correlation of circulating pro‐angiogenic mi RNA s’ expressions with risk, clinicopathological features, and survival profiles in gastric cancer ( GC ). Three hundred and thirty‐three GC patients underwent radical resection and 117 health controls ( HC s) were recruited for this study. Plasma samples were obtained from GC patients before the operation and from HC s after enrollment. Fourteen pro‐angiogenic mi RNA s were asseassed by quantitative polymerase chain reaction ( qPCR ). Disease‐free survival ( DFS ) and overall survival ( OS ) of GC patients were calculated and the median follow‐up duration was 36.0 months. Seven out of 14 pro‐angiogenic mi RNA s including let‐7f, miR‐17‐5p, miR‐18a, miR‐19b‐1, miR‐20a, miR‐210, and miR‐296 were observed to be elevated in GC patients compared with HC s. MiR‐18a, miR‐20a, and miR‐210 disclosed good predictive values of GC risk. Six pro‐angiogenic mi RNA s including miR‐17‐5p, miR‐92a, miR‐210, miR‐20a, miR‐18a, and miR‐296 expressions were positively while 1 pro‐angiogenic mi RNA (miR‐130a) was negatively correlated with tumor malignancy degree in GC patients. K‐M curve disclosed that 5 pro‐angiogenic mi RNA s including miR‐17‐5p, miR‐18a, miR‐20a, miR‐92a, and miR‐210 correlated with worse DFS , while 4 pro‐angiogenic mi RNA s including miR‐17‐5p, miR‐18a, miR‐20a, and miR‐210 associated with shorter OS . Further multivariate Cox's analysis revealed that miR‐17‐5p, miR‐18a, miR‐20a, and miR‐210 were independent predictive factors for unfavorable DFS and OS . In conclusion, circulating pro‐angiogenic mi RNA s could serve as novel noninvasive biomarkers for disease risk and malignancy degree, and miR‐17‐5p, miR‐18a, miR‐20a, and miR‐210 are independent factors predicting poor prognosis in GC patients.