SPNS2 promotes the malignancy of colorectal cancer cells via regulating Akt and ERK pathway

Clin Exp Pharmacol Physiol. 2019 Sep;46(9):861-871. doi: 10.1111/1440-1681.13124. Epub 2019 Jun 30.

Abstract

Colorectal cancer (CRC) is a prevalent malignant tumour that causes considerable cancer-related deaths globally. The sphingolipid transporter 2 (SPNS2), a sphingosine-1-phosphate (S1P) transporter, modulates multiple biological events including malignancy of cancer cells. In this study, the effects of SPNS2 on CRC progression were studied. We found that SPNS2 expression was significantly upregulated in CRC tissues compared to that in adjacent non-tumour tissues. To assess the role of SPNS2 in CRC cells, we performed loss- and gain-of-function experiments in SW480 and HCT116 cells, respectively. The results demonstrated that SPNS2 promoted proliferation, migration and invasion, and inhibited apoptosis in CRC cells. Additionally, SPNS2 enhanced the release of intracellular S1P, and increased S1P receptor 1 (S1PR1) and S1PR3 expression. Moreover, SPNS2 activated the Akt and ERK pathways, and the biological behaviours of SPNS2 were attenuated by Akt or ERK inhibitor in HCT116 cells. In conclusion, our results demonstrated that SPNS2 promoted proliferation, migration and invasion, and inhibited apoptosis by regulating S1P/S1PR1/3 axis and activating Akt and ERK pathway in CRC cells.

Keywords: ERK; Akt; apoptosis; colorectal cancer; proliferation; sphingolipid transporter 2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anion Transport Proteins / deficiency
  • Anion Transport Proteins / genetics
  • Anion Transport Proteins / metabolism*
  • Apoptosis
  • Base Sequence
  • Cell Movement
  • Cell Proliferation
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / pathology*
  • Female
  • Gene Expression Regulation, Neoplastic
  • Gene Knockdown Techniques
  • Gene Silencing
  • HCT116 Cells
  • Humans
  • MAP Kinase Signaling System*
  • Male
  • Middle Aged
  • Neoplasm Invasiveness
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Sphingosine-1-Phosphate Receptors / metabolism

Substances

  • Anion Transport Proteins
  • S1PR1 protein, human
  • Sphingosine-1-Phosphate Receptors
  • Spns2 protein, human
  • sphingosine-1-phosphate receptor-3, human
  • Proto-Oncogene Proteins c-akt