PLoS ONE (Jan 2014)

ADAM9 up-regulates N-cadherin via miR-218 suppression in lung adenocarcinoma cells.

  • Yuh-Pyng Sher,
  • Li-Ju Wang,
  • Li-Ling Chuang,
  • Mong-Hsun Tsai,
  • Ting-Ting Kuo,
  • Cheng-Chung Huang,
  • Eric Y Chuang,
  • Liang-Chuan Lai

DOI
https://doi.org/10.1371/journal.pone.0094065
Journal volume & issue
Vol. 9, no. 4
p. e94065

Abstract

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Lung cancer is the leading cause of cancer death worldwide, and brain metastasis is a major cause of morbidity and mortality in lung cancer. CDH2 (N-cadherin, a mesenchymal marker of the epithelial-mesenchymal transition) and ADAM9 (a type I transmembrane protein) are related to lung cancer brain metastasis; however, it is unclear how they interact to mediate this metastasis. Because microRNAs regulate many biological functions and disease processes (e.g., cancer) by down-regulating their target genes, microRNA microarrays were used to identify ADAM9-regulated miRNAs that target CDH2 in aggressive lung cancer cells. Luciferase assays and western blot analysis showed that CDH2 is a target gene of miR-218. MiR-218 was generated from pri-mir-218-1, which is located in SLIT2, in non-invasive lung adenocarcinoma cells, whereas its expression was inhibited in aggressive lung adenocarcinoma. The down-regulation of ADAM9 up-regulated SLIT2 and miR-218, thus down-regulating CDH2 expression. This study revealed that ADAM9 activates CDH2 through the release of miR-218 inhibition on CDH2 in lung adenocarcinoma.