Betulinic acid decreases expression of bcl-2 and cyclin D1, inhibits proliferation, migration and induces apoptosis in cancer cells

被引:0
作者
Wojciech Rzeski
Andrzej Stepulak
Marek Szymański
Marco Sifringer
Józef Kaczor
Katarzyna Wejksza
Barbara Zdzisińska
Martyna Kandefer-Szerszeń
机构
[1] Maria Curie-Skłodowska University,Department of Virology and Immunology, Institute of Microbiology and Biotechnology
[2] Technical University,Department of Pediatric Neurology
[3] Nicolaus Copernicus University,Department of Obstetrics, Women’s Diseases and Oncological Gynecology, Collegium Medicum
[4] Institute of Agricultural Medicine,Department of Toxicology
[5] Medical University Lublin,Department of Biochemistry and Molecular Biology
来源
Naunyn-Schmiedeberg's Archives of Pharmacology | 2006年 / 374卷
关键词
Betulinic acid; Proliferation; Migration; Apoptosis; Bcl-2; Cyclin D1;
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摘要
Betulinic acid (BA) is a pentacyclic triterpene found in many plant species, among others in the bark of white birch Betula alba. BA was reported to display a wide range of biological effects, including antiviral, antiparasitic, antibacterial and anti-inflammatory activities, and in particular to inhibit growth of cancer cells. The aim of the study was further in vitro characterization of BA anticancer activity. In this study, we demonstrated a remarkable antiproliferative effect of BA in all tested tumor cell cultures including neuroblastoma, rabdomyosarcoma-medulloblastoma, glioma, thyroid, breast, lung and colon carcinoma, leukemia and multiple myeloma, as well as in primary cultures isolated from ovarian carcinoma, cervical carcinoma and glioblastoma multiforme. Furthermore, we have shown that BA decreased cancer cell motility and induced apoptotic cell death. We also observed decrease of bcl2 and cyclin D1 genes expression, and increase of bax gene expression after betulinic acid treatment. These findings demonstrate the anticancer potential of betulinic acid and suggest that it may be taken into account as a supportive agent in the treatment of cancers with different tissue origin.
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页码:11 / 20
页数:9
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