| Literature DB >> 29616122 |
Xu-Feng Deng1,2, Dong Zhou1, Quan-Xing Liu1, Hong Zheng3, Yan Ding4, Wen-Yue Xu4, Jia-Xin Min1, Ji-Gang Dai1.
Abstract
Blocking the activation of nuclear factor κB (NF-κB) is a promising strategy for the treatment of non-small cell lung cancer. The circumsporozoite protein (CSP), a key component of the sporozoite stage of the malaria parasite, was previously reported to block NF-κB activation in hepatocytes. Therefore, in the present study, the effect of CSP on the growth of the human lung cancer cell line, A549, was investigated. It was demonstrated that transfection with a recombinant plasmid expressing CSP was able to inhibit the proliferation of A549 cells in a dose-dependent manner and induce the apoptosis of A549 cells. A NF-κB gene reporter assay indicated that CSP and its nuclear localization signal (NLS) motif were able to equally suppress the activation of NF-κB following stimulation with human recombinant tumor necrosis factor (TNF)-α in A549 cells. Furthermore, western blot analysis indicated that NLS did not affect the phosphorylation and degradation of IκB, but was able to markedly inhibit the nuclear translocation of NF-κB in TNF-α stimulated A549 cells. Therefore, the data suggest that CSP may be investigated as a potential novel NF-κB inhibitor for the treatment of lung cancer.Entities:
Keywords: apoptosis; circumsporozoite protein; human lung cancer cell line; nuclear transcription factor κb; proliferation
Year: 2018 PMID: 29616122 PMCID: PMC5876457 DOI: 10.3892/ol.2018.8115
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967