Identification of retinoic acid-regulated nuclear matrix-associated protein as a novel regulator of gastric cancer

Br J Cancer. 2009 Aug 18;101(4):691-8. doi: 10.1038/sj.bjc.6605202.

Abstract

Background: Retinoic acid-regulated nuclear matrix-associated protein (RAMP) is a WD40 repeat-containing protein that is involved in various biological functions, but little is known about its role in human cancer. This study aims to delineate the oncogenic role of RAMP in gastric carcinogenesis.

Methods: RAMP expression was examined by real-time quantitative RT-PCR, immunohistochemistry and western blotting. Inhibition of RAMP expression was performed by siRNA-mediated knockdown. The functional effects of RAMP on cell kinetics were measured by cell viability assay, colony formation assay and flow cytometry. Cell lines stably expressing RAMP were established to investigate the oncogenic effects of RAMP in vitro.

Results: Ramp was readily expressed in all seven gastric cancer cell lines and was significantly increased in human gastric cancer tissues when compared with their adjacent non-cancerous tissues (P<0.001). In keeping with this, expression of RAMP protein was higher in gastric cancer tissues compared with their adjacent non-cancerous tissues, whereas moderate protein expression were noted in intestinal metaplasia. Knockdown of RAMP in gastric cancer cells significantly reduced cell proliferation (P<0.01) and soft agar colony formation (P<0.001), but induced apoptosis and G(2)/M arrest. In additional, knockdown RAMP induced cell apoptosis is dependent on functional accumulation of p53 and p21 and induction of cleaved caspases-9, caspases-3 and PARP. Strikingly, overexpression of RAMP promoted anchorage-independent cell growth in soft agar.

Conclusion: Our findings demonstrate that RAMP plays an oncogenic role in gastric carcinogenesis. Inhibition of RAMP may be a promising approach for gastric cancer therapy.

MeSH terms

  • Apoptosis / physiology
  • Biomarkers, Tumor / analysis*
  • Blotting, Western
  • Cell Line, Tumor
  • Flow Cytometry
  • Gene Expression
  • Humans
  • Immunohistochemistry
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism*
  • RNA, Messenger / analysis
  • RNA, Small Interfering
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / metabolism*
  • Tissue Array Analysis
  • Ubiquitin-Protein Ligases

Substances

  • Biomarkers, Tumor
  • DTL protein, human
  • Nuclear Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Ubiquitin-Protein Ligases