Downregulation of MAGE family member H1 enhances hepatocellular carcinoma progression and serves as a biomarker for patient prognosis

Future Oncol. 2018 May;14(12):1177-1186. doi: 10.2217/fon-2017-0672. Epub 2018 Jan 10.

Abstract

Aim: The MAGE family member H1 (MAGEH1) belongs to melanoma-associated antigen (MAGE) superfamily. The role of MAGEH1 in hepatocellular carcinoma (HCC) is largely undefined.

Materials & methods: We used quantitative reverse transcription PCR and immunohistochemistry to detect MAGEH1 expression in HCC tissues. CCK-8 assay, wound healing migration assay and Transwell Matrigel invasion assay were used to measure HCC cell proliferation, migration and invasion ability.

Results: MAGEH1 expression was downregulated in HCC tumor tissues compared with adjacent normal liver tissues and in samples from patients with tumor recurrence. MAGEH1 reduced HCC cell proliferation, migration and invasion ability. Low MAGEH1 expression was significantly correlated with poor prognosis in HCC patients.

Conclusion: MAGEH1 may serve as a potential biomarker and a new prognostic factor for HCC.

Keywords: MAGEH1; hepatocellular carcinoma; prognosis.

MeSH terms

  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Carcinoma, Hepatocellular / mortality
  • Carcinoma, Hepatocellular / pathology*
  • Carcinoma, Hepatocellular / surgery
  • Cell Line, Tumor
  • Disease Progression
  • Down-Regulation
  • Female
  • Gene Knockdown Techniques
  • Humans
  • Liver / pathology
  • Liver / surgery
  • Liver Neoplasms / mortality
  • Liver Neoplasms / pathology*
  • Liver Neoplasms / surgery
  • Male
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism*
  • Middle Aged
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Neoplasm Recurrence, Local / diagnosis*
  • Neoplasm Recurrence, Local / epidemiology
  • Prognosis
  • Survival Rate

Substances

  • Biomarkers, Tumor
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • cytoplasmic linker protein 170