Retinoic acid receptor antagonists inhibit miR-10a expression and block metastatic behavior of pancreatic cancer

Gastroenterology. 2009 Dec;137(6):2136-45.e1-7. doi: 10.1053/j.gastro.2009.08.065. Epub 2009 Sep 10.


Background & aims: The infiltrating ductal adenocarcinoma of the pancreas is among the most lethal of all solid malignancies, largely owing to a high frequency of early metastasis. We identified microRNA-10a (miR-10a) as an important mediator of metastasis formation in pancreatic tumor cells and investigated the upstream and downstream regulatory mechanisms of miR-10a.

Methods: Northern blot analysis revealed increased expression levels of miR-10a in metastatic pancreatic adenocarcinoma. The role of miR-10a was analyzed by Morpholino and short interfering RNA transfection of pancreatic carcinoma cell lines and resected specimens of human pancreatic carcinoma. Metastatic behavior of primary pancreatic tumors and cancer cell lines was tested in xenotransplantation experiments in zebrafish embryos.

Results: We show that miR-10a expression promotes metastatic behavior of pancreatic tumor cells and that repression of miR-10a is sufficient to inhibit invasion and metastasis formation. We further show that miR-10a is a retinoid acid target and that retinoic acid receptor antagonists effectively repress miR-10a expression and completely block metastasis. This antimetastatic activity can be prevented by specific knockdown of HOX genes, HOXB1 and HOXB3. Interestingly, suppression of HOXB1 and HOXB3 in pancreatic cancer cells is sufficient to promote metastasis formation.

Conclusions: These findings suggest that miR-10a is a key mediator of metastatic behavior in pancreatic cancer, which regulates metastasis via suppression of HOXB1 and HOXB3. Inhibition of miR-10a expression (with retinoic acid receptor antagonists) or function (with specific inhibitors) is a promising starting point for antimetastatic therapies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / secondary
  • Adenocarcinoma / therapy*
  • Animals
  • Antigens, CD
  • Benzoates / pharmacology*
  • Blotting, Northern
  • Cadherins / metabolism
  • Cell Line, Tumor
  • Chromans / pharmacology*
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Genetic Therapy* / methods
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Humans
  • MicroRNAs / metabolism*
  • Morpholines / metabolism
  • Neoplasm Invasiveness
  • Oligonucleotides, Antisense / metabolism
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / metabolism
  • Pancreatic Neoplasms / secondary
  • Pancreatic Neoplasms / therapy*
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Receptors, Retinoic Acid / antagonists & inhibitors*
  • Receptors, Retinoic Acid / genetics
  • Receptors, Retinoic Acid / metabolism
  • Retinoids / pharmacology
  • Transfection
  • Up-Regulation
  • Xenograft Model Antitumor Assays
  • Zebrafish / embryology
  • alpha Catenin / metabolism
  • beta Catenin / metabolism


  • Antigens, CD
  • Benzoates
  • CDH1 protein, human
  • CTNNB1 protein, human
  • Cadherins
  • Chromans
  • HOXB1 homeodomain protein
  • Homeodomain Proteins
  • HoxB3 protein, human
  • MicroRNAs
  • Morpholines
  • Oligonucleotides, Antisense
  • RNA, Small Interfering
  • Receptors, Retinoic Acid
  • Retinoids
  • alpha Catenin
  • beta Catenin
  • Ro 41-5253