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

Abstract
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.
AuthorsZhengyi Zhang, Jingnan Pi, Dongling Zou, Xiaoshuang Wang, Jiayue Xu, Shan Yu, Ting Zhang, Feng Li, Xianxie Zhang, Hualu Zhao, Fang Wang, Dong Wang, Yanni Ma, Jia Yu
JournalNature communications (Nat Commun) Vol. 10 Issue 1 Pg. 4397 (09 27 2019) ISSN: 2041-1723 [Electronic] England
PMID31562301 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • MIRN574 microRNA, human
  • MicroRNAs
Topics
  • Animals
  • Cell Line, Tumor
  • Cell Movement (genetics)
  • Cell Proliferation (genetics)
  • Disease Progression
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Male
  • Mice, Inbred BALB C
  • Mice, Inbred NOD
  • Mice, SCID
  • MicroRNAs (genetics)
  • Middle Aged
  • RNA Interference
  • RNAi Therapeutics (methods)
  • Stomach Neoplasms (genetics, pathology)
  • Xenograft Model Antitumor Assays (methods)

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