Effect of senescence-associated secretory phenotype-conditioned medium on proliferation of human gastric cancer cell lines BGC823
10.16781/j.0258-879x.2017.12.1508
- Author:
Yu WANG
1
Author Information
1. Department of General Surgery (II), Changzheng Hospital, Second Military Medical University
- Publication Type:Journal Article
- Keywords:
Cell proliferation;
Cell senescence;
Gastric carcinoma;
Senescence-associated secretory phenotype;
Taxol
- From:
Academic Journal of Second Military Medical University
2017;38(12):1508-1513
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effect of senescence-associated secretory phenotype-conditioned medium (SASP-CM) on the proliferation of human gastric cancer cell lines BGC823. Methods BGC823 cells were divided into three groups: SASP-CM group, tumor cells control-conditioned medium (CTR-CM) group, and normal-conditioned medium (NOR-CM) group. BGC823 cells in theSASP-CM group were treated with paclitaxel (PTX) to establish senescent cell model and to prepare SASP-CM. The establishment of senescent cell model was confirmed by senescence- associated (Fgalactosidase staining. The concentrations of major SASP factors in SASP-CM were detected by enzyme linked lmmunosorbent assay, the proliferationability ofBGC823 cells was detected by CCK-8 assay and cell clone formation assay, and the cell cycle and apoptosis were detected by flow cytometry. Results After treating BGC823 cells with 35 nmol/L PTX for 72 h, a steady senescence modll was established, which had the highest percentage of senescence cells ([66.95±3.54]%). The concentrations of lnterleukin (IL)-6, IL-8, chemokine (C-X-Cmotif) ligand 1 (CXCL1), chemokine (C-C motif) ligand 2 (CCL2), and lnterferon γ (INF-γ) in the SASP-CM were significantly higher than those ln the CTR-CM (all P<0.01). The relative clone formation rate of BGC823 cells in the SASP-CM group was significantly higher than those ln the CTR-CM group (P<0.01) and NOR-CM group (P<0. 05). The proliferation activity of BGC823 cells in the SASP-CM group was significantly higher than that in the CTR-CM and NOR-CM groups after incubation for 48, 72 and 96 h (all P<0.05). The percentage of S phase cells in the SASP-CM group was significantly higher than that in the CTR-CM and NOR-CM groups (both P<0.01), and there was no significant difference in cell apoptosis rate between groups. Conclusion SASP-CM can promote the proliferation of human gastric cancer cell lines BGC823.
