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microRNA arm-imbalance in part from complementary targets mediated decay promotes gastric cancer progression
microRNA arm-imbalance in part from complementary targets mediated decay promotes gastric cancer progression
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microRNA arm-imbalance in part from complementary targets mediated decay promotes gastric cancer progression
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microRNA arm-imbalance in part from complementary targets mediated decay promotes gastric cancer progression
microRNA arm-imbalance in part from complementary targets mediated decay promotes gastric cancer progression

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microRNA arm-imbalance in part from complementary targets mediated decay promotes gastric cancer progression
microRNA arm-imbalance in part from complementary targets mediated decay promotes gastric cancer progression
Journal Article

microRNA arm-imbalance in part from complementary targets mediated decay promotes gastric cancer progression

2019
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Overview
Strand-selection is the final step of microRNA biogenesis in which functional mature miRNAs are generated from one or both arms of precursor. The preference of strand-selection is diverse during development and tissue formation, however, its pathological effect is still unknown. Here we find that two miRNA arms from the same precursor, miR-574-5p and miR-574-3p, are inversely expressed and play exactly opposite roles in gastric cancer progression. Higher-5p with lower-3p expression pattern is significantly correlated with higher TNM stages and poor prognosis of gastric cancer patients. The increase of miR-574-5p/-3p ratio, named miR-574 arm-imbalance is partially due to the dynamic expression of their highly complementary targets in gastric carcinogenesis, moreover, the arm-imbalance of miR-574 is in turn involved and further promotes gastric cancer progression. Our results indicate that miR-574 arm-imbalance contribute to gastric cancer progression and re-modification of the miR-574-targets homeostasis may represent a promising strategy for gastric cancer therapy. Functional miRNAs derived from the 5p or 3p arm of some miRNA duplexes have opposite roles in cancer progression. Here, the authors show that oncogenic miR-574-5p has greater preference in aggressive gastric cancer as compared with miR-574-3p and this arm preference is partly dependent on complementary targets mediated miRNA decay.