The cardiac glycoside convallatoxin inhibits the growth of colorectal cancer cells in a p53-independent manner

被引:17
作者
Anderson, Sarah E. [1 ]
Barton, Christopher E. [1 ]
机构
[1] Belmont Univ, Dept Biol, 1900 Belmont Blvd, Nashville, TN 37211 USA
来源
MOLECULAR GENETICS AND METABOLISM REPORTS | 2017年 / 13卷
关键词
Cancer; Apoptosis; Cell cycle; Convallatoxin; p53; UP-REGULATION; APOPTOSIS; P53; MECHANISMS; EXPRESSION; ATPASE; PUMA; P21; P73;
D O I
10.1016/j.ymgmr.2017.07.011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cardiac glycosides are plant-derived molecules that have shown antiproliferative properties against cancer cells, though the mechanism of action is not completely understood. We show that one cardiac glycoside, convallatoxin, presents antiproliferative effects against colorectal cancer cells in culture and that the resulting cell death is independent of the p53 tumor suppressor. Our data suggest that convallatoxin may be useful in the treatment of cancers that harbor inactivating mutations in the p53 signaling pathway.
引用
收藏
页码:42 / 45
页数:4
相关论文
共 28 条
[1]   Inhibition of DNA topoisomerases I and II, and growth inhibition of breast cancer MCF-7 cells by ouabain, digoxin and proscillaridin A [J].
Bielawski, Krzysztof ;
Winnicka, Katarzyna ;
Bielawska, Anna .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (07) :1493-1497
[2]   Requirement for p53 and p21 to sustain G2 arrest after DNA damage [J].
Bunz, F ;
Dutriaux, A ;
Lengauer, C ;
Waldman, T ;
Zhou, S ;
Brown, JP ;
Sedivy, JM ;
Kinzler, KW ;
Vogelstein, B .
SCIENCE, 1998, 282 (5393) :1497-1501
[3]   Cytotoxic Effects of Cardiac Glycosides in Colon Cancer Cells, Alone and in Combination with Standard Chemotherapeutic Drugs [J].
Felth, Jenny ;
Rickardson, Linda ;
Rosen, Josefin ;
Wickstrom, Malin ;
Fryknas, Marten ;
Lindskog, Magnus ;
Bohlin, Lars ;
Gullbo, Joachim .
JOURNAL OF NATURAL PRODUCTS, 2009, 72 (11) :1969-1974
[4]   Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012 [J].
Ferlay, Jacques ;
Soerjomataram, Isabelle ;
Dikshit, Rajesh ;
Eser, Sultan ;
Mathers, Colin ;
Rebelo, Marise ;
Parkin, Donald Maxwell ;
Forman, David ;
Bray, Freddie .
INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (05) :E359-E386
[5]   E1A activates transcription of p73 and noxa to induce apoptosis [J].
Flinterman, M ;
Guelen, L ;
Ezzati-Nik, S ;
Killick, R ;
Melino, G ;
Tominaga, K ;
Mymryk, JS ;
Gäken, J ;
Tavassoli, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (07) :5945-5959
[6]  
FREY T, 1995, CYTOMETRY, V21, P265, DOI 10.1002/cyto.990210307
[7]   Identification of a network involved in thapsigargin-induced apoptosis using a library of small interfering RNA expression vectors [J].
Futami, T ;
Miyagishi, M ;
Taira, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (01) :826-831
[8]   Ex Vivo Activity of Cardiac Glycosides in Acute Leukaemia [J].
Hallbook, Helene ;
Felth, Jenny ;
Eriksson, Anna ;
Fryknas, Marten ;
Bohlin, Lars ;
Larsson, Rolf ;
Gullbo, Joachim .
PLOS ONE, 2011, 6 (01)
[9]   Digitoxin is a potential anticancer agent for several types of cancer [J].
Haux, J .
MEDICAL HYPOTHESES, 1999, 53 (06) :543-548
[10]   Up-regulation of Bcl-2 homology 3 (BH3)-only proteins by E2F1 mediates apoptosis [J].
Hershko, T ;
Ginsberg, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (10) :8627-8634