Purpose: To study the expression of insulin-like growth factor binding proteins (IGFBPs) in paclitaxel-treatedgastric cancer SGC-7901 cells, and to further investigate underlying mechanisms. Materials and Methods: Realtime PCR and Western blot assays were applied to detect the mRNA and protein expression of IGFBP-2, -3 and-5 after paclitaxel (10 nM) treatment of SGC-7901 cells. In addition IGFBP-3 expression was silenced by RNAinterference to determine effects. Cell viability was determined by MTT assay. Cell cycling and apoptosis wereassessed by flow cytometry. Results: Compared to the control group, only IGFBP-3 expression was elevatedsignificantly after paclitaxel (10 nM) treatment (p<0.05). Paclitaxel treatment caused cell cycle arrest and apoptosisvia downregulating Bcl-2 expression. However, the effect could be abrogated by IGFBP-3 silencing. Conclusions:IGFBP-3 exhibits anti-apoptotic effects on paclitaxel-treated SGC-7901 cells via elevating Bcl-2 expression.
(2014). Expression and Underlying Roles of IGFBP-3 in Paclitaxel-Treated Gastric Cancer Sgc-7901 Cells. Asian Pacific Journal of Cancer Prevention, 15(14), 5741-5745.
MLA
. "Expression and Underlying Roles of IGFBP-3 in Paclitaxel-Treated Gastric Cancer Sgc-7901 Cells". Asian Pacific Journal of Cancer Prevention, 15, 14, 2014, 5741-5745.
HARVARD
(2014). 'Expression and Underlying Roles of IGFBP-3 in Paclitaxel-Treated Gastric Cancer Sgc-7901 Cells', Asian Pacific Journal of Cancer Prevention, 15(14), pp. 5741-5745.
VANCOUVER
Expression and Underlying Roles of IGFBP-3 in Paclitaxel-Treated Gastric Cancer Sgc-7901 Cells. Asian Pacific Journal of Cancer Prevention, 2014; 15(14): 5741-5745.