h-Prune is associated with poor prognosis and epithelial-mesenchymal transition in patients with colorectal liver metastases

Int J Cancer. 2016 Aug 15;139(4):812-23. doi: 10.1002/ijc.30118. Epub 2016 Apr 21.

Abstract

The prognosis of patients with colorectal liver metastases (CRLM) remains low despite advances in chemotherapy and surgery. The expression of h-prune (human homolog of Drosophila prune protein; HGNC13420), an exopolyphosphatase, is correlated with progression and aggressiveness in several cancers and promotes migration and invasion. We investigated the role of h-prune in CRLM. To investigate the role of h-prune, immunohistochemical analysis for h-prune was performed in 87 surgically resected specimens of CRLM obtained between 2001 and 2009 at the Hiroshima University Hospital. Immunohistochemical analysis revealed positive staining for h-prune in 24 (28%) cases. The overall survival rate was significantly lower in h-prune-positive cases than in h-prune-negative cases (p = 0.003). Multivariate analysis showed that h-prune positivity was the only independent factor related to poor overall survival of patients after curative hepatectomy of CRLM. In vitro and in vivo, h-prune-knocked-down and h-prune-overexpressing cells were analyzed. In vitro, h-prune was associated with increased cell motility and upregulation of epithelial-mesenchymal transition (EMT) markers. In a mouse model, h-prune was associated with invasion of the tumor and distant metastases. In summary, h-prune expression is a useful marker to identify high-risk patients for resectable colorectal liver metastasis. h-Prune expression is necessary for cancer cell motility and EMT and is associated with liver and lung metastasis in colorectal cancer cells. h-Prune could be a new prognostic marker and molecular target for CRLM.

Keywords: colorectal cancer; colorectal liver metastasis; epithelial-mesenchymal transition; h-prune; metastasis.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Biomarkers, Tumor*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / mortality*
  • Colorectal Neoplasms / pathology
  • Colorectal Neoplasms / surgery
  • Disease Models, Animal
  • Epithelial-Mesenchymal Transition* / genetics
  • Female
  • Humans
  • Immunohistochemistry
  • Liver Neoplasms / mortality*
  • Liver Neoplasms / secondary*
  • Male
  • Mice
  • Middle Aged
  • Neoplasm Grading
  • Neoplasm Metastasis
  • Phosphoric Monoester Hydrolases
  • Prognosis
  • Young Adult

Substances

  • Biomarkers, Tumor
  • Carrier Proteins
  • PRUNE1 protein, human
  • Phosphoric Monoester Hydrolases