Sasa veitchii extract exhibits antitumor effect against murine pancreatic adenocarcinoma in vivo and in vitro

被引:0
|
作者
Hamanaka, Junya [1 ]
Mikami, Yurie [2 ]
Horiuchi, Ayane [3 ]
Yano, Aiko [2 ]
Amano, Fumiya [3 ]
Shibata, Suo [3 ]
Ogata, Aya [3 ]
Ogata, Kenichi [2 ]
Nagatsu, Akito [4 ]
Miura, Nobuhiko [5 ]
Sano, Makoto [6 ,7 ]
Suzui, Masumi [1 ]
Yoshioka, Hiroki [3 ,4 ,8 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Neurotoxicol, Nagoya, Japan
[2] Kyushu Univ, Fac Dent Sci, Div Maxillofacial Diagnost & Surg Sci, Sect Oral & Maxillofacial Oncol, Fukuoka, Japan
[3] Gifu Univ Med Sci, Fac Pharm, 4-3-3 Nijigaoka, Kani, Gifu 5090293, Japan
[4] Kinjo Gakuin Univ, Coll Pharm, Nagoya, Japan
[5] Yokohama Univ Pharm, Dept Hlth Sci, Yokohama, Japan
[6] Nihon Univ, Sch Med, Dept Anesthesiol, Tokyo, Japan
[7] Natl Inst Occupat Safety & Hlth, Dept Toxicol Test Methodol Dev, Hazard Evaluat Test & Res Area, Fujisawa, Japan
[8] Kitasato Univ, Sch Med, Dept Hyg, Sagamihara, Japan
基金
日本学术振兴会;
关键词
cell cycle arrest; PDAC; Sasa veitchii; sodium copper chlorophyllin; CELL-CYCLE ARREST; CANCER PREVENTION; PHENOLIC-COMPOUNDS; LEAF EXTRACT; INVOLVEMENT; INVASION; STEMNESS;
D O I
10.1002/tkm2.1441
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
AimSasa veitchii extract (SE) has been used as a traditional medicine to treat halitosis, stomatitis, gingivitis, and pressure ulcers. SE exerts various antimicrobial, antiviral, and antitumor effects. Although SE has the potential to inhibit breast, colon, and lung cancer cells, it remains unknown whether these effects can also be applied to other types of cancer. In this study, we explored the antitumor effects of SE in murine pancreatic ductal adenocarcinoma (PDAC) cells both in vivo and in vitro.MethodsFor in vitro experiments, we examined cell proliferation after 48 hours. We evaluated the apoptosis-and cell-cycle-related molecules using immunocytochemistry and immunoblot analyses. For the in vivo study, we evaluated the tumor volume and weight during three weeks of SE administration using an allograft model.ResultsSE showed the antitumor effect in a dose- and time-dependent manner. SE treatment induced apoptosis in higher dose (400 mu g/mL) and induced the downregulation of cyclin-dependent kinases Cdk4/Cdk6 and Cyclin D1 in lower dose (200 mu g/mL). In a murine allograft model, tumor volume and weight were reduced by SE administration.ConclusionSE exhibits an antitumor effect against murine PDAC cells in vivo and in vitro.
引用
收藏
页码:10 / 19
页数:10
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