Upregulation of nemo-like kinase is an independent prognostic factor in colorectal cancer

World J Gastroenterol. 2015 Aug 7;21(29):8836-47. doi: 10.3748/wjg.v21.i29.8836.

Abstract

Aim: To investigate the expression and oncogenic role of nemo-like kinase (NLK) in colorectal cancer.

Methods: Expression of NLK protein was assessed by immunohistochemistry in tissue specimens from 56 cases of normal colorectal mucosa, 51 cases of colorectal adenoma, and 712 cases of colorectal cancer. In addition, NLK expression was knocked down using a lentivirus carrying NLK small hairpin RNA in colorectal cancer cells. Cell viability methylthiazoletetrazolium assays, colony formation assays, flow cytometry cell cycle assays, Transwell migration assays, and gene expression assays were performed to explore its role on proliferation and migration of colorectal cancer.

Results: Expression of NLK protein progressively increased in tissues from the normal mucosa through adenoma to various stages of colorectal cancer. Overexpression of NLK protein was associated with advanced tumor-lymph node-metastasis stages, poor differentiation, lymph node and distant metastases, and a higher recurrence rate of colorectal cancer (P < 0.05). Multivariate analyses showed that NLK expression was an independent prognostic factor to predict overall survival (hazard ratio 2.57, 95% confidence interval: 1.66-3.98; P < 0.001) and disease-free survival (hazard ratio 1.96, 95% confidence interval: 1.40-2.74: P < 0.001) of colorectal cancer patients. Furthermore, knockdown of NLK expression in colorectal cancer cell lines reduced cell viability, colony formation, and migration, and arrested tumor cells at the G0/G1 phase of the cell cycle. At the gene level, knockdown of NLK expression inhibited matrix metalloproteinase-2 expression in colorectal cancer cells.

Conclusion: NLK overexpression is an independent prognostic factor in colorectal cancer and knockdown of NLK expression inhibits colorectal cancer progression and metastasis.

Keywords: Colorectal cancer; Gene regulation; Nemo-like kinase; Prognosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenomatous Polyps / enzymology*
  • Adenomatous Polyps / genetics
  • Adenomatous Polyps / mortality
  • Adenomatous Polyps / pathology
  • Adenomatous Polyps / surgery
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Carcinoma / enzymology*
  • Carcinoma / genetics
  • Carcinoma / mortality
  • Carcinoma / secondary
  • Carcinoma / surgery
  • Cell Cycle Checkpoints
  • Cell Movement
  • Cell Proliferation
  • Cell Survival
  • Colonic Polyps / enzymology*
  • Colonic Polyps / genetics
  • Colonic Polyps / mortality
  • Colonic Polyps / pathology
  • Colonic Polyps / surgery
  • Colorectal Neoplasms / enzymology*
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / mortality
  • Colorectal Neoplasms / pathology
  • Colorectal Neoplasms / surgery
  • Disease Progression
  • Disease-Free Survival
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Neoplastic
  • HCT116 Cells
  • HEK293 Cells
  • HT29 Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Lymphatic Metastasis
  • Multivariate Analysis
  • Neoplasm Recurrence, Local
  • Neoplasm Staging
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • RNA Interference
  • Risk Factors
  • Transfection
  • Treatment Outcome
  • Up-Regulation

Substances

  • Biomarkers, Tumor
  • Intracellular Signaling Peptides and Proteins
  • NLK protein, human
  • Protein Serine-Threonine Kinases