Inhibition of fatty acid synthase by beta-lactones and other compounds for inhibition of cellular proliferation
The present invention features methods of treating a cancer in a subject by administering an effective amount of a beta-lactone to the subject. The invention also features methods of inhibiting angiogenesis in a subject by administering an effective amount of an inhibitor of fatty acid synthase to the subject. These methods can be used to treat a variety of cancers and other diseases and conditions. The invention also features methods of identifying beta-lactones and other compounds that can be used in the methods of the invention for the treatment of tumors, inhibition of angiogenesis, and the treatment of diseases and conditions that involve pathological angiogenesis.
1. A method of identifying a beta-lactone that inhibits tumor cell proliferation, comprising:
a) contacting a sample comprising tumor cells with a beta-lactone, wherein the beta-lactone has the formula I:
wherein R 1 , R 2 , R 3 , and R 4 are, independently, hydrogen, an alkyl group, a cycloalkyl group, a heterocyloalkyl group, an alkoxy group, a hydroxyalkyl group, a halogenated alkyl group, an alkoxyalkyl group, an alkenyl group, an alkynyl group, an aryl group, a heteroaryl group, an aralkyl group, a hydroxy group, an amine group, an amide, an ester, a carbonate group, a carboxylic acid, an aldehyde, a keto group, an ether group, a halide, a urethane group, a silyl group, or a sulfo-oxo group, and wherein the stereochemistry at carbons a and b is R or S; and
b) measuring the amount of cell proliferation, cell cycle progression, cell cycle arrest, or apoptosis in the sample exposed to the beta-lactone,
whereby a decrease in cell proliferation, a decrease in cell cycle progression, an increase in cell cycle arrest, or an increase in apoptosis in the sample comprising tumor cells exposed to the beta-lactone, relative to the amount of proliferation, cell cycle progression, cell cycle arrest, or apoptosis in a sample comprising tumor cells not contacted with the beta-lactone, identifies a beta-lactone that inhibits proliferation of a tumor cell.
2. The method of claim 1 wherein R 1 is a straight alkyl group.
3. A method of identifying a beta-lactone that inhibits angiogenesis, comprising:
a) contacting a sample comprising endothelial cells with a beta-lactone having the formula I:
wherein R 1 , R 2 , R 3 , and R 4 are, independently, hydrogen, an alkyl group, a cycloalkyl group, a heterocyloalkyl group, an alkoxy group, a hydroxyalkyl group, a halogenated alkyl group, an alkoxyalkyl group, an alkenyl group, an alkynyl group, an aryl group, a heteroaryl group, an aralkyl group, a hydroxy group, an amine group, an amide, an ester, a carbonate group, a carboxylic acid, an aldehyde, a keto group, an ether group, a halide, a urethane group, a silyl group, or a sulfo-oxo group, and wherein the stereochemistry at carbons a and b is R or S; and
b) measuring the amount of endothelial cell proliferation, cell cycle progression, or cell cycle arrest in the sample,
whereby a decrease in cell proliferation, a decrease in cell cycle progression, or an increase in cell cycle arrest in the sample, relative to the amount of cell proliferation, cell cycle progression, or cell cycle arrest in a sample comprising endothelial cells not contacted with the beta-lactone, identifies a beta-lactone that inhibits angiogenesis.
4. The method of claim 3 wherein R 1 is a straight alkyl group.
5. A method of identifying a beta-lactone that inhibits angiogenesis, comprising:
a) contacting a sample with a beta-lactone, wherein the sample comprises angiogenic cells and wherein the beta-lactone has the formula I:
wherein R 1 , R 2 , R 3 , and R 4 are, independently, hydrogen, an alkyl group, a cycloalkyl group, a heterocyloalkyl group, an alkoxy group, a hydroxyalkyl group, a halogenated alkyl group, an alkoxyalkyl group, an alkenyl group, an alkynyl group, an aryl group, a heteroaryl group, an aralkyl group, a hydroxy group, an amine group, an amide, an ester, a carbonate group, a carboxylic acid, an aldehyde, a keto group, an ether group, a halide, a urethane group, a silyl group, or a sulfo-oxo group, and wherein the stereochemistry at carbons a and b is R or S, and
b) measuring the amount of angiogenesis in the sample,
whereby a decrease in the amount of angiogenesis in the sample, relative to the amount of angiogenesis in a sample not contacted with the beta-lactone, identifies a beta-lactone that inhibits angiogenesis.
6. The method of claim 5 wherein R 1 is a straight alkyl group.