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Pulsatilla Decoction and its bioactive component β-peltatin induce G2/M cell cycle arrest and apoptosis in pancreatic cancer
被引:3
|作者:
Wu, Rong
[1
,2
]
Xi, Zhichao
[1
,2
]
Liu, Mengfan
[1
,2
]
Ren, Hangui
[1
,2
]
Dai, Rongchen
[1
,2
]
Jiang, Xue
[1
,2
]
Nabil, Wan Najbah Nik
[1
,2
,3
]
Wang, Yalin
[1
,2
]
Feng, Jiling
[1
,2
]
Chai, Qiong
[1
,2
]
Dong, Qihan
[4
,5
,6
]
Xu, Hongxi
[1
,2
]
机构:
[1] Shanghai Univ Tradit Chinese Med, Sch Pharm, Shanghai 201203, Peoples R China
[2] Engn Res Ctr Shanghai Coll TCM New Drug Discovery, Shanghai 201203, Peoples R China
[3] Minist Hlth, Pharmaceut Serv Program, Petaling Jaya 46200, Selangor, Malaysia
[4] Univ Sydney, Fac Med & Hlth, Cent Clin Sch, Chinese Med Anticanc Evaluat Program,Greg Brown La, Sydney, NSW 2006, Australia
[5] Univ Sydney, Fac Med & Hlth, Charles Perkins Ctr, Sydney, NSW 2006, Australia
[6] Royal Prince Alfred Hosp, Dept Endocrinol, Sydney, NSW 2050, Australia
基金:
中国国家自然科学基金;
关键词:
Pulsatilla Decoction;
Pulsatilla;
beta-peltatin;
Pancreatic cancer;
G2/M arrest;
Apoptosis;
D O I:
10.1186/s13020-023-00774-0
中图分类号:
R [医药、卫生];
学科分类号:
10 ;
摘要:
Background Pancreatic cancer (PAC), a malignancy that is fatal and commonly diagnosed at a late stage. Despite considerable advancements in cancer treatment, the survival rate of PAC remains largely consistent for the past 60 years. The traditional Chinese medicine formula Pulsatilla Decoction (PD) has been clinically used to treat inflammatory diseases for millennia and recently as a supplementary anti-cancer treatment in China. However, the bioactive ingredients and mechanisms underlying its anti- cancer effect remains unclear. Methods The composition and quality control of PD were verified through analysis by high performance liquid chromatography. Cell viability was determined using Cell Counting Kit-8 assay. The cell cycle distribution was analyzed through PI staining and flow cytometry analysis, while apoptotic cells were measured by double staining with Annexin V-FITC and PI. We used immunoblotting to examine protein expressions. The in vivo effects of ss-peltatin and podophyllotoxin were evaluated on a subcutaneously-xenografted BxPC-3 cell nude mice model. Results The current study demonstrated that PD markedly inhibited PAC cell proliferation and triggered their apoptosis. Four herbal PD formula was then disassembled into 15 combinations of herbal ingredients and a cytotoxicity assay showed that the Pulsatillae chinensis exerted the predominant anti-PAC effect. Further investigation indicated that ss-peltatin was potently cytotoxic with -IC50 of similar to 2 nM. ss-peltatin initially arrested PAC cells at G2/M phase, followed by apoptosis induction. Animal study confirmed that ss-peltatin significantly suppressed the growth of subcutaneously-implanted BxPC-3 cell xenografts. Importantly, compared to podophyllotoxin that is the parental isomer of ss-peltatin but clinically obsoleted due to its severe toxicity, ss-peltatin exhibited stronger anti-PAC effect and lower toxicity in mice. Conclusions Our results demonstrate that Pulsatillae chinensis and particularly its bioactive ingredient ss-peltatin suppress PAC by triggering cell cycle arrest at G2/M phase and apoptosis.
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