Ding Lu, Shao Shu-Li, He Meng-Qi, Huang Xin, Zhang Wei-Wei, Zhang Zhen-Zhu
College of Life Science and Agriculture and Forestry.
Heilongjiang Provincial Key Laboratory of Resistance Gene Engineering and Protection of Biodiversity in Cold Areas, Qiqihar University, Qiqihaer 161000, China.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2021 Sep;37(5):495-499. doi: 10.12047/j.cjap.6091.2021.060.
To investigate the effects of betulinic acid on apoptosis of human gastric cancer SGC-7901 cells. The human gastric cancer SGC-7901cells were divided in to 4 groups, and each group was set with 3 replicates. The SGC-7901cells in control group were not treated with betulinic acid; the other 3 experimental groups were treated with betulinic acid at the concentrations of 10, 20 and 30 mg/L, respectively; each group was incubated in a 5% carbon dioxide incubator for 48 h. Laser confocal microscope was used to observe morphological changes of SGC-7901 cells; Flow cytometry was applied to determine apoptosis rate and mitochondrial membrane potential. The mRNA and protein levels of , and were also detected by qRT-PCR and western blot respectively. Compared with the control group, SGC-7901 cells in the treated group at final concentrations of 10, 20 and 30 mg/L shrinked, appeared apoptosis body along with nuclear splitting. The percentage of cells in early and advanced period of apoptosis were markedly increased (<0.05 or <0.01), mitochondrial membrane potential was obviously reduced (<0.05 or <0.01). qRT-PCR and western blot analysis showed that the mRNA and protein expressions of and were increased significantly (<0.01), while the expressions of were decreased significantly (<0.01). Within a certain range of concentrations, betulinic acid induces cell apoptosis by regulating the expression of , and in human gastric cancer.