TY - JOUR
T1 - 龙血竭抗癌成分的虚拟筛选及体外抗癌活性检测验证
AU - Liu, Fang
AU - Dai, Rongji
AU - Lü, Fang
AU - Deng, Yulin
N1 - Publisher Copyright:
© 2023 Beijing Institute of Technology. All rights reserved.
PY - 2023/4
Y1 - 2023/4
N2 - To study anticancer compounds of dragon’s blood, taking HER2 as the target protein receptor, 149 known compounds were virtually screened based on computer-aided screening technology. The potential active components were tested for the effects on HER2 activity in vitro and the anticancer activity on human breast cancer cell SK-BR-3. The results show that the molecular docking model of the HER2 target protein possesses stronger enrichment ability for active molecules. The molecules that can effectively dock with HER2 and have anticancer potential are mainly dihydrochalcones, flavanes, steroids and stilbenes. Among them, four can bind to extracellular and intracellular domain of HER2, and three can bind to intracellular domain of HER2, they all have significant inhibitory effects on HER2 in vitro. Trans-3-methoxy-4',5-dihydroxystilbene and trans-3,4',5-trihydroxystilbene show significant anticancer effects on SK-Br-3 in vitro and can inhibit cancer cell proliferation, change cell cycle, and cause SK-Br-3 very significant apoptosis, which provide a basis data for the development of dragon's blood anticancer drugs.
AB - To study anticancer compounds of dragon’s blood, taking HER2 as the target protein receptor, 149 known compounds were virtually screened based on computer-aided screening technology. The potential active components were tested for the effects on HER2 activity in vitro and the anticancer activity on human breast cancer cell SK-BR-3. The results show that the molecular docking model of the HER2 target protein possesses stronger enrichment ability for active molecules. The molecules that can effectively dock with HER2 and have anticancer potential are mainly dihydrochalcones, flavanes, steroids and stilbenes. Among them, four can bind to extracellular and intracellular domain of HER2, and three can bind to intracellular domain of HER2, they all have significant inhibitory effects on HER2 in vitro. Trans-3-methoxy-4',5-dihydroxystilbene and trans-3,4',5-trihydroxystilbene show significant anticancer effects on SK-Br-3 in vitro and can inhibit cancer cell proliferation, change cell cycle, and cause SK-Br-3 very significant apoptosis, which provide a basis data for the development of dragon's blood anticancer drugs.
KW - anticancer activity in vitro
KW - anticancer ingredient
KW - dragon’s blood
KW - virtual screening
UR - http://www.scopus.com/inward/record.url?scp=85170278017&partnerID=8YFLogxK
U2 - 10.15918/j.tbit1001-0645.2022.132
DO - 10.15918/j.tbit1001-0645.2022.132
M3 - 文章
AN - SCOPUS:85170278017
SN - 1001-0645
VL - 43
SP - 429
EP - 438
JO - Beijing Ligong Daxue Xuebao/Transaction of Beijing Institute of Technology
JF - Beijing Ligong Daxue Xuebao/Transaction of Beijing Institute of Technology
IS - 4
ER -