HE Xiao-yi1, SHEN Xian-rong2, LIU Qiong2, et al. Antitumor Effect in vitro of Compound Fomes fomentarius[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(3): 188-191.
HE Xiao-yi1, SHEN Xian-rong2, LIU Qiong2, et al. Antitumor Effect in vitro of Compound Fomes fomentarius[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(3): 188-191. DOI: 10.13422/j.cnki.syfjx.2013.03.064.
木蹄复方体外抗肿瘤作用的实验研究
摘要
目的:筛选木蹄复方抗肿瘤活性提取物
初步分析其化学成分并观察其体外抗肿瘤效应。方法:常规水提和醇提的方法提取复方中水溶和醇溶性组分。MTT法测定木蹄复方水提取物(distilled water extract of compound Fomes fomentarius
WECF)和木蹄复方乙醇提取物(ethanol extract of compound F.fomentarius
Objective:To screen the antitumor extract of compound Fomes fomentarius
detect its chemical composition preliminarily and evaluate its antitumor activity in vitro.Method: Distilled water or ethanol was used for extraction of compound F.fomentarius.The MTT assay was used to measure the inhibition effect in vitro of distilled water extract of compound F.fomentarius(WECF) and ethanol extract of compound F.fomentarius(EECF).The system pre-test method was used to detect the chemical composition preliminarily.Apoptosis of A549 was tested by flow cytometry.Result: The 50% inhibition concentration(IC50) of WECF to A549
Hela and QGY were(0.28±0.02)
(0.40±0.06)
(0.28±0.05) g · L-1 respectively
and to EECF
the IC50 were(0.50±0.04)
(0.50±0.03)
(0.60±0.06) g · L-1 respectively.There were organic acid
amino acid
peptides and proteins
sugar
polysaccharide and nucleoside
saponins
lactone
coumarone and nucleoside
plant sterol and terpene composition
volatile oil and grease in WECF.The polysaccharide content of WECF was(16.1±0.5)%.The IC50 of WECF to A549
Hela
QGY
DU145
MDA-MB-435S and SGC-7901 were 0.29
0.45
0.32
0.32
0.83
0.23 g · L-1.22.0% of totle cells apoptosis after A549 treating with WECF at 1 g · L-1 for 24 h.Conclusion: WECF showed higher antitumor activity in vitro compared with EECF and has significant inhibitory effect to a variety of tumor cells
further investigation revealed that WECF exerted an antitumor activity via apoptosis-induced cell death and maybe developed as a new antitumor medicine.