Enhanced activation of PERK-ATF4 pathway by Brefeldin A and cisplatin in human lung cancer GLC-82 ;cells
10.3969/j.issn.1006-5725.2016.14.015
- VernacularTitle:布雷菲德菌素A联合顺铂增强肺癌GLC-82细胞PERK-ATF4通路的激活水平
- Author:
Mingsong WU
;
Xiang ZHENG
;
Nana GENG
;
Zhimin ZHANG
;
Yanyu ZHAO
;
Zhe WANG
;
Xueying LI
- Publication Type:Journal Article
- Keywords:
Lung cancer;
PERK;
ATF4;
Endoplasmic reticulum stress;
Brefeldin A;
CDDP
- From:
The Journal of Practical Medicine
2016;32(14):2302-2305
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the molecular mechanisms of synergistic effects of BFA and CDDP on human lung cancer GLC-82 cells, and to test the levels of PERK-ATF4 pathway. Methods GLC-82 cells were incubated with 50 ng/mL of BFA or/and 2 μg/mL of CDDP for 24 or 48 hours. The levels of PERK, p-PERK and ATF4 in GLC-82 were analyzed by real-time PCRand/or Western Blot. Results The levels of PERK were lowest in CDDP group, but higher in BFA group (P < 0.05), the highest in group of BFA+CDDP (P < 0.05 or P < 0.01). The p-PERK level decreased in group of BFA+CDDP (P < 0.05 or P < 0.01). There was no significant change of ATF4 expression in CDDP group, but ATF4 expression increased slightly in BFA group, and increased further in group of BFA+CDDP (P < 0.05 or P < 0.01)which was also higher than that in BFA group or CDDP group (P < 0.05 or P < 0.01). Conclusions The upregulated levels of PERK and ATF4 by the combination of BFA and CDDP may be one of the mechanisms of synergistic anti-cancer effect of BFA and CDDP on GLC-82 cells.