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Mol Cancer Ther ; 5(9): 2300-9, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16985064

ABSTRACT

Phytochemicals have provided an abundant and effective source of therapeutics for the treatment of cancer. Here we describe the characterization of a novel plant toxin, persin, with in vivo activity in the mammary gland and a p53-, estrogen receptor-, and Bcl-2-independent mode of action. Persin was previously identified from avocado leaves as the toxic principle responsible for mammary gland-specific necrosis and apoptosis in lactating livestock. Here we used a lactating mouse model to confirm that persin has a similar cytotoxicity for the lactating mammary epithelium. Further in vitro studies in a panel of human breast cancer cell lines show that persin selectively induces a G2-M cell cycle arrest and caspase-dependent apoptosis in sensitive cells. The latter is dependent on expression of the BH3-only protein Bim. Bim is a sensor of cytoskeletal integrity, and there is evidence that persin acts as a microtubule-stabilizing agent. Due to the unique structure of the compound, persin could represent a novel class of microtubule-targeting agent with potential specificity for breast cancers.


Subject(s)
Apoptosis Regulatory Proteins/physiology , Apoptosis/drug effects , Breast Neoplasms/drug therapy , Fatty Alcohols/pharmacology , Membrane Proteins/physiology , Persea/chemistry , Proto-Oncogene Proteins/physiology , Animals , Antineoplastic Agents, Phytogenic/pharmacology , Apoptosis/physiology , Apoptosis Regulatory Proteins/biosynthesis , Bcl-2-Like Protein 11 , Breast Neoplasms/genetics , Breast Neoplasms/pathology , Cell Cycle/drug effects , Cell Division/drug effects , Cell Growth Processes/drug effects , Cell Line, Tumor , Fatty Alcohols/isolation & purification , G2 Phase/drug effects , Humans , Lactation , Mammary Glands, Animal/drug effects , Mammary Glands, Animal/pathology , Membrane Proteins/biosynthesis , Mice , Microtubules/drug effects , Microtubules/metabolism , Plant Leaves/chemistry , Proto-Oncogene Proteins/biosynthesis , Proto-Oncogene Proteins c-bcl-2/biosynthesis , Proto-Oncogene Proteins c-bcl-2/genetics , Transfection
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