A Potential Anti-cancer Compound Separated from the Chloroform Extract of the Chinese Medicine Formula Shenqi San

Lu Shi , Yi-jun Tu , Si-qi Ye , Yu Xia , Chao-zhi Ma , Xiao-zhi Peng , Yan-wen Liu , Zhong-zhu Ai , Peng-tao You

Current Medical Science ›› 2020, Vol. 40 ›› Issue (1) : 138 -144.

PDF
Current Medical Science ›› 2020, Vol. 40 ›› Issue (1) : 138 -144. DOI: 10.1007/s11596-020-2157-5
Article

A Potential Anti-cancer Compound Separated from the Chloroform Extract of the Chinese Medicine Formula Shenqi San

Author information +
History +
PDF

Abstract

This study examined anti-cancer compounds present in the chloroform extract of the Chinese medicine formula Shenqi San (CE-SS). Silica gel column chromatography, Sephadex LH-20, octadecylsilyl (ODS) column chromatography, and high performance liquid chromatography (HPLC) were used to separate the compounds from CE-SS. The structural formulas of the separated compounds were determined using 1D 1H and 13C experiments as well as high resolution electrospray ionization mass spectroscopy (HRESIMS). The corresponding results were compared with the reported literature data. A total of six compounds were separated and their structures were identified on the basis of corresponding spectroscopic and physico-chemical properties. They were Saikogenin F (I), Prosaikogenin D (II), Prosaikogenin F (III), β-sitosterol (IV), 3β,16β,23-trihydroxy-13,28-epoxyurs-11-ene-3-O-β-D-glucopyranoside (V), and methyl ursolic acid (VI). The separated compounds were evaluated in vitro for their inhibitory ability against the proliferation of A549 cells via MTT assay. Apoptosis was investigated using Annexin V-FITC/propidium iodide (PI) by flow cytometry. Apoptosis-associated proteins were examined by Western blotting. All the compounds were observed to have inhibitory activities against the proliferation of A549 cells to different degrees. Flow cytometry showed that compound V increased the proportion of apoptotic A549 cells in a dose-dependent manner. Western blotting showed that compound V increased the expression of Bax, cleaved-caspase-3, cleaved-caspase-9 and cleaved-poly ADP-ribose polymerase (PARP), and decreased the expression of Bcl-2. These results indicated that compound V featured a significant inhibitory effect on A549 cells when compared with other compounds, and it may be considered a potential drug against cancers.

Keywords

Shenqi San / separation / identification / A549 / apoptosis

Cite this article

Download citation ▾
Lu Shi, Yi-jun Tu, Si-qi Ye, Yu Xia, Chao-zhi Ma, Xiao-zhi Peng, Yan-wen Liu, Zhong-zhu Ai, Peng-tao You. A Potential Anti-cancer Compound Separated from the Chloroform Extract of the Chinese Medicine Formula Shenqi San. Current Medical Science, 2020, 40(1): 138-144 DOI:10.1007/s11596-020-2157-5

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

ChenW, ZhengR, BaadePD, et al.. Cancer statistics in China, 2015. CA Cancer J Clin, 2016, 66(2): 115-132

[2]

SiegelRL, MillerKD, JemalA. Cancer statistics, 2018. CA Cancer J Clin, 2018, 68(1): 7-30

[3]

ChenZ, FillmoreCM, HammermanPS, et al.. Non-small-cell lung cancers: a heterogeneous set of diseases. Nat Rev Cancer, 2014, 14(8): 535-546

[4]

ShiL, AiZZ, ZhangDZ, et al.. Anti-Tumor and Analgesic Effects of Shenqi powder. Med J Wuhan Univ (Chinese), 2016, 37(3): 411-413

[5]

XiaY, ShiL, AiZZ, et al.. Chinese medicine formula “Shenqi San” extract inhibits proliferation of human lung adenocarcinoma A549 cells via inducing apoptosis. J Huazhong Univ Sci Technolog Med Sci, 2017, 37(5): 766-771

[6]

HouJQ, GuoC, ZhaoJJ, et al.. Anti-inflammatory Meroterpenoids from Baeckea frutescens. J Nat Prod, 2017, 80(8): 2204-2214

[7]

ZhuZJ, PanRL, SiJY. Study on the Chemical constituents of Bupleurum bicaule. Nat Prod Res Dev, 2008, 20: 833-835

[8]

MencheriniT, PicernoP, ScesaC, et al.. Triterpene, antioxidant, and antimicrobial compounds from Melissa officinalis. J Nat Prod, 2007, 70(12): 1889-1894

[9]

YeL, QianJ, JinS, et al.. Algicidal effects of four Chinese herb extracts on bloom-forming Microcystis aeruginosa and Chlorella pyrenoidosa. Environ Technol, 2014, 35(9–12): 1150-1156

[10]

MoreiraH, SlezakA, SzyjkaA, et al.. Antioxidant and Cancer Chemopreventive Activities of Cistus and Pomegranate Polyphenols. Acta Pol Pharm, 2017, 74(2): 688-698

[11]

PossebonL, LebronIDL, da SilvaLF, et al.. Anti-inflammatory actions of herbal medicines in a model of chronic obstructive pulmonary disease induced by cigarette smoke. Biomed Pharmacother, 2018, 99(2018): 591-597

[12]

XiaY, YuB, MaC, et al.. Yu Gan Long reduces rat liver fibrosis by blocking TGF-beta1/Smad pathway and modulating the immunity. Biomed Pharmacother, 2018, 106: 1332-1338

[13]

YouP, FuS, YuK, et al.. Scutellarin suppresses neuroinflammation via the inhibition of the AKT/NF-kappaB and p38/JNK pathway in LPS-induced BV-2 microglial cells. Naunyn Schmiedebergs Arch Pharmacol, 2018, 391(7): 743-751

[14]

MohammadRM, MuqbilI, LoweL, et al.. Broad targeting of resistance to apoptosis in cancer. Semin Cancer Biol, 2015, 35: S78-S103

[15]

WangJ, LiJZ, LuAX, et al.. Anticancer effect of salidroside on A549 lung cancer cells through inhibition of oxidative stress and phospho-p38 expression. Oncol Lett, 2014, 7(4): 1159-1164

[16]

WangX, WangD, ZhaoY. Effect and Mechanism of Resveratrol on the Apoptosis of Lung Adenocarcinoma Cell Line A549. Cell Biochem Biophys, 2015, 73(2): 527-531

[17]

YeMX, ZhangJ, ZhangJ, et al.. Curcumin promotes apoptosis by activating the p53-miR-192-5p/215-XIAP pathway in non-small cell lung cancer. Cancer Lett, 2015, 357(1): 196-205

[18]

PhamTA, ShairM I, VuVT, et al.. Phloroglucinol Derivatives from the Fruits of Eucalyptus globulus and Their Cytotoxic Activities. Chem Biodivers, 2018, 15(6): e1800052

[19]

ZhouS, WangY, ZhuJJ. Simultaneous Detection of Tumor Cell Apoptosis Regulators Bcl-2 and Bax through a Dual-Signal-Marked Electrochemical Immunosensor. ACS Appl Mater Interfaces, 2016, 8(12): 7674-7682

[20]

CzabotarPE, LesseneG, StrasserA, et al.. Control of apoptosis by the BCL-2 protein family: implications for physiology and therapy. Nat Rev Mol Cell Biol, 2014, 15(1): 49-63

[21]

GolestaniE B, SanatiMH, HoushmandM, et al.. Expression and prognostic significance of bcl-2 and bax in the progression and clinical outcome of transitional bladder cell carcinoma. Cell J, 2014, 15(4): 356-363

[22]

WhiteMJ, McArthurK, MetcalfD, et al.. Apoptotic caspases suppress mtDNA-induced STING-mediated type I IFN production. Cell, 2014, 159(7): 1549-1562

[23]

ShaliniS, DorstynL, DawarS, et al.. Old, new and emerging functions of caspases. Cell Death Differ, 2015, 22(4): 526-539

[24]

YouleRJ, StrasserA. The BCL-2 protein family: opposing activities that mediate cell death. Nat Rev Mol Cell Biol, 2008, 9(1): 47-59

[25]

LeeDH, KimDW, JungCH, et al.. Gingerol sensitizes TRAIL-induced apoptotic cell death of glioblastoma cells. Toxicol Appl Pharmacol, 2014, 279(3): 253-265

[26]

ZhangF, ShiJJ, ThakurK, et al.. Anti-Cancerous Potential of Polysaccharide Fractions Extracted from Peony Seed Dreg on Various Human Cancer Cell Lines Via Cell Cycle Arrest and Apoptosis. Front Pharmacol, 2017, 8: 102

AI Summary AI Mindmap
PDF

105

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/