miR-27a induced by colon cancer cells in HLECs promotes lymphangiogenesis by targeting SMAD4

PLoS One. 2017 Oct 24;12(10):e0186718. doi: 10.1371/journal.pone.0186718. eCollection 2017.

Abstract

Aim: Metastasis of tumor cells occurs through lymphatic vessels, blood vessels and transcoelomic spreading. Growing evidence from in vivo and in vitro studies has indicated that tumor lymphangiogenesis facilitates metastasis. However, the regulation of lymphangiogenesis in colon cancer remains unclear. The aims of this study were to identify key miRNAs in colon cancer lymphangiogenesis and to investigate its target and mechanism.

Methods: miRNA microarray analysis was conducted to identify miRNAs in human lymphatic endothelial cells (HLECs) that were regulated by co-cultured human colon cancer cells. Gain- and loss-of-function studies were performed to determine the function of miR-27a, a top hint, on lymphangiogenesis and migration in HLECs. Furthermore, bioinformatics prediction and experimental validation were performed to identify miR-27a target genes in lymphangiogenesis.

Results: We found that expression of miR-27a in HLECs was induced by co-culturing with colon cancer cells. Over-expression of miR-27a in HLECs enhanced lymphatic tube formation and migration, whereas inhibition of miR-27a reduced lymphatic tube formation and migration. Luciferase reporter assays showed that miR-27a directly targeted SMAD4, a pivotal component of the TGF-β pathway. In addition, gain-of-function and loss-of-function experiments showed that SMAD4 negatively regulated the length of lymphatic vessels formed by HLECs and migration.

Conclusions: Our data indicated that colon cancer cell induced the expression of miR-27a in HLECs, which promoted lymphangiogenesis by targeting SMAD4. Our finding implicated miR-27a as a potential target for new anticancer therapies in colon cancer.

MeSH terms

  • Cells, Cultured
  • Coculture Techniques
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • Humans
  • Lymphangiogenesis / physiology*
  • Lymphatic Vessels / cytology*
  • MicroRNAs / biosynthesis
  • MicroRNAs / physiology*
  • Signal Transduction
  • Transforming Growth Factor beta / metabolism

Substances

  • MIRN27 microRNA, human
  • MicroRNAs
  • Transforming Growth Factor beta

Grants and funding

This work was supported by the National Natural Science Foundation of China (No. 81000929 to JLT, 81401437 to CPZ; https://isisn.nsfc.gov.cn/egrantindex/funcindex/prjsearch-list#). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.