Hypomethylation-mediated activation of cancer/testis antigen KK-LC-1 facilitates hepatocellular carcinoma progression through activating the Notch1/Hes1 signalling

Cell Prolif. 2019 May;52(3):e12581. doi: 10.1111/cpr.12581. Epub 2019 Mar 20.

Abstract

Objectives: Kita-Kyushu lung cancer antigen-1 (KK-LC-1) is a cancer/testis antigen reactivated in several human malignancies. So far, the major focus of studies on KK-LC-1 has been on its potential as diagnostic biomarker and immunotherapy target. However, its biological functions and molecular mechanisms in cancer progression remain unknown.

Materials and methods: Expression of KK-LC-1 in HCC was analysed using RT-qPCR, Western blot and immunohistochemistry. The roles of KK-LC-1 on HCC progression were examined by loss-of-function and gain-of-function approaches. Pathway inhibitor DAPT was employed to confirm the regulatory effect of KK-LC-1 on the downstream Notch signalling. The interaction of KK-LC-1 with presenilin-1 was determined by co-immunoprecipitation. The association of CpG island methylation status with KK-LC-1 reactivation was evaluated by methylation-specific PCR, bisulphite sequencing PCR and 5-Aza-dC treatment.

Results: We identified that HCC tissues exhibited increased levels of KK-LC-1. High KK-LC-1 level independently predicted poor survival outcome. KK-LC-1 promoted cell growth, migration, invasion and epithelial-mesenchymal transition in vitro and in vivo. KK-LC-1 modulated the Notch1/Hes1 pathway to exacerbate HCC progression through physically interacting with presenilin-1. Upregulation of KK-LC-1 in HCC was attributed to hypomethylated CpG islands.

Conclusions: This study identified that hypomethylation-induced KK-LC-1 overexpression played an important role in HCC progression and independently predicted poor survival. We defined the KK-LC-1/presenilin-1/Notch1/Hes1 as a novel signalling pathway that was involved in the growth and metastasis of HCC.

Keywords: Cancer/testis antigen; KK-LC-1; epithelial-mesenchymal transition; hepatocellular carcinoma; methylation.

MeSH terms

  • Animals
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / metabolism*
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / metabolism*
  • Carcinoma, Hepatocellular / pathology
  • Cell Line, Tumor
  • CpG Islands
  • DNA Methylation
  • Disease Progression
  • Epithelial-Mesenchymal Transition
  • Gene Knockdown Techniques
  • Hep G2 Cells
  • Heterografts
  • Humans
  • Liver Neoplasms / genetics
  • Liver Neoplasms / metabolism*
  • Liver Neoplasms / pathology
  • Male
  • Mice
  • Mice, Nude
  • Presenilin-1 / metabolism
  • Prognosis
  • RNA, Small Interfering / genetics
  • Receptor, Notch1 / metabolism*
  • Signal Transduction
  • Transcription Factor HES-1 / metabolism*
  • Up-Regulation

Substances

  • Antigens, Neoplasm
  • CT83 protein, human
  • NOTCH1 protein, human
  • PSEN1 protein, human
  • Presenilin-1
  • RNA, Small Interfering
  • Receptor, Notch1
  • Transcription Factor HES-1
  • HES1 protein, human