Silencing of ST6GalNAc I suppresses the proliferation, migration and invasion of hepatocarcinoma cells through PI3K/AKT/NF-κB pathway

Tumour Biol. 2016 Sep;37(9):12213-12221. doi: 10.1007/s13277-016-5086-y. Epub 2016 May 27.

Abstract

ST6GalNAc I is the major Sialyl-Tn antigen (STn) synthase that is highly correlated with tumor invasion and metastasis. However, the roles and molecular mechanisms by which ST6GalNAc I mediates the malignant phenotypes of hepatocarcinoma cells still remain poorly unknown. In this study, we investigated the expression of STn and ST6GalNAc I in mouse hepatocarcinoma cell lines Hca-F, Hca-P, and Hepa1-6, which have different metastatic potential, as compared with normal mouse liver cell line IAR-20. The results showed that the expression of ST6GalNAc I and STn in Hca-F and Hca-P cells was much higher than that in Hepa1-6 and IAR20 cells. Knockdown of ST6GalNAc I by shRNA in Hca-F cells significantly decreased the expression of STn and inhibited the growth of tumor cells in vitro and in vivo. This reduction of ST6GalNAc I expression also led to the decreased migration and invasion of Hca-F cells. Furthermore, we found that ST6GalNAc I knockdown inhibited the expression levels of PI3k, p-Akt473, p-Akt308, NF-κB, and their downstream molecules. Together, our results suggest a role of ST6GalNAc I in promoting the growth and invasion of hepatocarcinoma cells through regulating PI3K/AKT signaling, and ST6GalNAc I might be a promising marker for the prognosis and therapy of hepatocarcinoma.

Keywords: Hepatocarcinoma; Invasion; Migration; Proliferation; ST6GalNAc I; STn.

MeSH terms

  • Animals
  • Antigens, Tumor-Associated, Carbohydrate / metabolism
  • Blotting, Western
  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / metabolism
  • Carcinoma, Hepatocellular / therapy
  • Cell Movement / genetics*
  • Cell Proliferation / genetics*
  • Immunohistochemistry
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / therapy
  • Mice, Inbred Strains
  • Microscopy, Fluorescence
  • NF-kappa B / metabolism
  • Neoplasm Invasiveness
  • Neoplasms, Experimental / genetics
  • Neoplasms, Experimental / metabolism
  • Neoplasms, Experimental / therapy
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • RNA Interference*
  • RNAi Therapeutics / methods
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sialyltransferases / genetics*
  • Sialyltransferases / metabolism
  • Signal Transduction

Substances

  • Antigens, Tumor-Associated, Carbohydrate
  • NF-kappa B
  • sialosyl-Tn antigen
  • Sialyltransferases
  • CMP-N-acetylneuraminate-alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt