TY - JOUR
T1 - Targeting mitochondrial apoptosis by betulinic acid in human cancers
AU - Fulda, Simone
AU - Kroemer, Guido
N1 - Funding Information:
This work has been supported by a joint project of Deutscher Akademischer Auslandsdienst (DAAD) and Institut National du Cancer (INCa). Simone Fulda is supported by grants from the Deutsche Forschungsgemeinschaft, the Deutsche Krebshilfe, the Bundesministerium für Forschung und Technologie, Wilhelm-Sander-Stiftung, Else-Kröner-Fresenius Stiftung, the European Community (ApopTrain, APO-SYS) and IAP6/18; Guido Kroemer by grants from Ligue contre le Cancer (laboratoire labelliseé), Institut Nationale du Cancer, Cancéropôle Ile-de-France, and the European Commission (ACTIVE P53, APO-SYS, ApopTrain, RIGHT).
PY - 2009/9/1
Y1 - 2009/9/1
N2 - Betulinic acid (BA) is a naturally occurring pentacyclic triterpene that exhibits a variety of biological activities including potent antitumor properties. This anticancer activity has been linked to its ability to directly trigger mitochondrial membrane permeabilization, a central event in the apoptotic process that seals the cell's fate. In contrast to the potent cytotoxicity of BA against a variety of cancer types, non-neoplastic cells as well as normal tissue remain relatively resistant to BA, thus pointing to a therapeutic window. Because agents that exert a direct action on mitochondria may bypass resistance to conventional chemotherapeutics, there is increasing interest to develop such compounds as experimental cancer therapeutics. Thus, mitochondrion-targeted agents such as BA hold great promise as a novel approach to overcome certain forms of drug resistance in human cancers.
AB - Betulinic acid (BA) is a naturally occurring pentacyclic triterpene that exhibits a variety of biological activities including potent antitumor properties. This anticancer activity has been linked to its ability to directly trigger mitochondrial membrane permeabilization, a central event in the apoptotic process that seals the cell's fate. In contrast to the potent cytotoxicity of BA against a variety of cancer types, non-neoplastic cells as well as normal tissue remain relatively resistant to BA, thus pointing to a therapeutic window. Because agents that exert a direct action on mitochondria may bypass resistance to conventional chemotherapeutics, there is increasing interest to develop such compounds as experimental cancer therapeutics. Thus, mitochondrion-targeted agents such as BA hold great promise as a novel approach to overcome certain forms of drug resistance in human cancers.
UR - http://www.scopus.com/inward/record.url?scp=69749094633&partnerID=8YFLogxK
U2 - 10.1016/j.drudis.2009.05.015
DO - 10.1016/j.drudis.2009.05.015
M3 - Review article
C2 - 19520182
AN - SCOPUS:69749094633
SN - 1359-6446
VL - 14
SP - 885
EP - 890
JO - Drug Discovery Today
JF - Drug Discovery Today
IS - 17-18
ER -