Overexpression of CXCL2 inhibits cell proliferation and promotes apoptosis in hepatocellular carcinoma

BMB Rep. 2018 Dec;51(12):630-635. doi: 10.5483/BMBRep.2018.51.12.140.


C-X-C motif chemokine ligand 2 (CXCL2) is a small secreted protein that exhibits a structure similar to the proangiogenic subgroup of the CXC chemokine family. Recently, accumulating evidence suggests that chemokines play a pivotal role in cancer progression and carcinogenesis. We examined the expression levels of 7 types of ELR+ CXCLs messenger RNA (mRNA) in 264 clinical samples. We found that CXCL2 expression was stably down-regulated in 94% of hepatocellular carcinoma (HCC) specimens compared with paired adjacent normal liver tissues and some HCC cell lines. Moreover, CXCL2 overexpression profoundly attenuated HCC cell proliferation and growth and induced apoptosis in vitro. In animal studies, we found that overexpressing CXCL2 by lentivirus also apparently inhibited the size and weight of subcutaneous tumours in nude mice. Furthermore, we demonstrated that CXCL2 induced HCC cell apoptosis via both nuclear and mitochondrial apoptosis pathways. Our results indicate that CXCL2 negatively regulates the cell cycle in HCC cells via the ERK1/2 signalling pathway. These results provide new insights into HCC and may ultimately lead to the discovery of innovative therapeutic approaches of HCC. [BMB Reports 2018; 51(12): 630-635].

MeSH terms

  • Animals
  • Apoptosis*
  • Carcinoma, Hepatocellular / metabolism
  • Carcinoma, Hepatocellular / pathology*
  • Cell Cycle Checkpoints
  • Cell Line, Tumor
  • Cell Proliferation*
  • Chemokine CXCL2 / antagonists & inhibitors
  • Chemokine CXCL2 / genetics
  • Chemokine CXCL2 / metabolism*
  • Down-Regulation
  • Female
  • Humans
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Middle Aged
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Signal Transduction


  • CXCL2 protein, human
  • Chemokine CXCL2
  • RNA, Small Interfering
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3