Microgreens: Functional Food with Antiproliferative Cancer Properties Influenced by Light.

The anti-proliferative/pro-oxidant efficacy of green pea, soybean, radish, Red Rambo radish, and rocket microgreens, cultivated under either fluorescent lighting (predominant spectral peaks in green and orange) or combination light-emitting diode (LED, predominant spectral peak in blue) was investigated using Ewing sarcoma lines, RD-ES and A673, respectively. All aqueous microgreen extracts significantly reduced cell proliferation (cancer prevention effect) to varying extents in two-dimensional sarcoma cell cultures. The effect of the polyphenol fraction in the aqueous food matrix was unrelated to total polyphenol content, which differed between species and light treatment. Only Pisum sativum (LED-grown) extracts exercised anti-proliferative and pro-apoptotic effects in both three-dimensional RD-ES and A673 spheroids (early tumor progression prevention), without cytotoxic effects on healthy L929 fibroblasts. A similar anti-tumor effect of Red Rambo radish (LED and fluorescent-grown) was evident only in the RD-ES spheroids. Aside from the promising anti-tumor potential of the polyphenol fraction of green pea microgreens, the latter also displayed favorable growth quality parameters, along with radish, under both light treatments over the 10 day cultivation period.

NKAP functions as an oncogene in Ewing sarcoma cells partly through the AKT signaling pathway.

NF-κB activating protein (NKAP) is a highly conserved protein involved in transcriptional repression, immune cell development, maturation, acquisition of functional competency and maintenance of hematopoiesis. In the present study, the function of NKAP in the progress of Ewing sarcoma (ES) was investigated. It was identified that NKAP is highly expressed in ES cells when compared with human mesenchymal stem cells (MSCs). NKAP was knocked-down in human ES cell lines A673 and RD-ES using small interfering (si)RNA transfection. The effectiveness of transfection was then verified using reverse transcription-quantitative PCR and western blot analysis to determine mRNA and protein levels, respectively. The results of the proliferation assays indicated that the knockdown of NKAP inhibited the proliferation and clonogenic abilities of human ES cells. Transwell assays further indicated that cell invasion and migration were significantly inhibited by NKAP knockdown, which may be mediated by downregulation of matrix metalloproteinase (MMP)-9 activity. Gain-of-function analysis also demonstrated the positive role NKAP played in the proliferation, invasion and migration of ES cells. Cell apoptosis was evaluated by flow cytometry, which identified that apoptotic cells were significantly increased when NKAP was silenced. In addition, downregulation of NKAP increased the levels of Bax and cleaved caspase 3, but decreased Bcl2 levels, which suggested that the mitochondrial apoptosis pathway was activated. To explore the action mechanism of NKAP, the status of the AKT signaling pathway in NKAP-silenced A673 and RD-ES cells was investigated. Results indicated that NKAP knockdown led to decreased phosphorylation of AKT and expression of cyclin D1, a down-stream effector of the AKT signaling pathway, suggesting inactivation of the AKT signaling pathway. In conclusion, the present study revealed that NKAP promoted the proliferation, migration and invasion of ES cells, at least partly, through the AKT signaling pathway, providing new approaches for the therapeutic application of NKAP in ES.

Inhibitory Effects of 5-aza-2'-deoxycytidine and Histone Deacetylase Inhibitors on RD-ES Cells in Culture / 环境与健康杂志

Objective To know the inhibitory effects of 5aza-CdR in combination with HDAC inhibitors on RD-ES cells in culture.Methods This study was to investigate that the HDAC inhibitors (MS-275,Trichostatin-A and depsipeptide)and 5azaCdR inhibition effect on RD-ES cells by MTT.High sensitivity DNA kit was used to detect DNA inhibition rate.RT-PCR method was used to detect the expression of ECAD and TSLC1 for 5aza-CdR joint Depsi on RD-ES cells.Results IC50 of 5aza-CdR for RD-ES cell was 40 ng/ml,for 48 h 50 % DNA inhibition rate,the concentration was approximately 50 ng/ml.IC50 of HDAC inhibitors (MS-275,trichostatin-A,Depsi) for RD-ES cell was 400 ng/ml,2.5 ng/ml and 0.6 ng/ml respectively.The inhibition rate of 5aza-CdR jointed HDAC inhibitors was significantly higher compared with the single used groups (P