Agents for reversing epigenetic silencing of genes
The present invention provides methods for discovering agents that are effective in reversing epigenetic silencing by inhibiting the interaction of methyl-binding (MBD) proteins with methylated genomic DNA. Also provided are methods for reactivating silenced genes having CpG island hypermethylation along with methods for treatment and prevention of diseases, such as cancer and sickle cell anemia, by administering an agent that modulates methyl-binding domain (MBD) protein-mediated transcriptional repression, thereby increasing gene transcription to prevent or treat disease. Additionally, compounds identified by the present invention useful for treatment and prevention of diseases, such as cancer and sickle cell anemia, are provided.
1. A method of treating prostate cancer associated with CpG island hypermethylation of a GSTP1 gene in a subject, the method comprising:
a) identifying a subject as having a prostate cancer with CpG island hypermethylation of a GSTP1 gene and/or epigenetic silencing of a GSTP1 gene mediated by a methyl-binding domain (“MBD”) family protein; and
b) administering to the subject a therapeutically effective amount of a compound of: structural formula (V):
or a pharmaceutically acceptable salt thereof.
2. The method of claim 1 , wherein the subject is a human.
3. The method of claim 1 , wherein the MBD family protein is MBD2.
4. A method for reversing epigenetic silencing of a GSTP1 gene in a cancer cell, the method comprising contacting a cancer cell with an effective amount of a compound of:
structural formula (V):
or a pharmaceutically acceptable salt thereof, wherein the cancer cell is a prostate cancer cell, a breast cancer cell, or a liver cancer cell, and wherein the contacting is in vitro.
5. The method of claim 4 , wherein the epigenetic silencing is mediated by an MBD family protein.
6. The method of claim 5 , wherein the MBD family protein is MBD2.
7. A method of treating prostate cancer associated with CpG island hypermethylation of a GSTP1 gene in a subject in need of such treatment, the method comprising administering to the subject a therapeutically effective amount of a compound of structural formula (V):
or a pharmaceutically acceptable salt thereof.
8. A method of treating breast cancer comprising:
a) identifying a subject as having breast cancer associated with epigenetic silencing of a GSTP1 gene mediated by MBD2; and
b) administering to the subject a therapeutically effective amount of a composition comprising a compound of structural formula (V):
or a pharmaceutically acceptable salt thereof and a chemotherapeutic agent.
9. The method of claim 8 , wherein the chemotherapeutic agent is selected from the group consisting of Aclacinomycins, Actinomycins, Adriamycins, Ancitabines, Anthramycins, Azacitidines, Azaserines, 6-Azauridines, Bisantrenes, Bleomycins, Cactinomycins, Carmofurs, Carmustines, Carubicins, Carzinophilins, Chromomycins, Cisplatins, Cladribines, Cytarabines, Dactinomycins, Daunorubicins, Denopterins, 6-Diazo-5-Oxo-L-Norleucines, Doxifluridines, Doxorubicins, Edatrexates, Emitefurs, Enocitabines, Fepirubicins, Fludarabines, Fluorouracils, Gemcitabines, Idarubicins, Loxuridines, Menogarils, 6-Mercaptopurines, Methotrexates, Mithramycins, Mitomycins, Mycophenolic Acids, Nogalamycins, Olivomycines, Peplomycins, Pirarubicins, Piritrexims, Plicamycins, Porfiromycins, Pteropterins, Puromycins, Retinoic Acids, Streptonigrins, Streptozocins, Tagafurs, Tamoxifens, Thiamiprines, Thioguanines, Triamcinolones, Trimetrexates, Tubercidins, Vinblastines, Vincristines, Zinostatins, and Zorubicins.
10. The method of claim 8 , wherein the chemotherapeutic agent is selected from the group consisting of Doxorubicins, Fluorouracils, Gemcitabines, Methotrexates, Tamoxifens, and Vinblastines.
11. A method of treating breast cancer associated with CpG island hypermethylation of a GSTP1 gene in a subject having breast cancer associated with CpG island hypermethylation of a GSTP1 gene, the method comprising administering to the subject a therapeutically effective amount of a composition comprising a compound of structural formula (V):
or a pharmaceutically acceptable salt thereof and a chemotherapeutic agent.
12. The method of claim 11 , wherein the chemotherapeutic agent is selected from the group consisting of Aclacinomycins, Actinomycins, Adriamycins, Ancitabines, Anthramycins, Azacitidines, Azaserines, 6-Azauridines, Bisantrenes, Bleomycins, Cactinomycins, Carmofurs, Carmustines, Carubicins, Carzinophilins, Chromomycins, Cisplatins, Cladribines, Cytarabines, Dactinomycins, Daunorubicins, Denopterins, 6-Diazo-5-Oxo-L-Norleucines, Doxifluridines, Doxorubicins, Edatrexates, Emitefurs, Enocitabines, Fepirubicins, Fludarabines, Fluorouracils, Gemcitabines, Idarubicins, Loxuridines, Menogarils, 6-Mercaptopurines, Methotrexates, Mithramycins, Mitomycins, Mycophenolic Acids, Nogalamycins, Olivomycines, Peplomycins, Pirarubicins, Piritrexims, Plicamycins, Porfiromycins, Pteropterins, Puromycins, Retinoic Acids, Streptonigrins, Streptozocins, Tagafurs, Tamoxifens, Thiamiprines, Thioguanines, Triamcinolones, Trimetrexates, Tubercidins, Vinblastines, Vincristines, Zinostatins, and Zorubicins.
13. The method of claim 11 , wherein the chemotherapeutic agent is selected from the group consisting of Doxorubicins, Fluorouracils, Gemcitabines, Methotrexates, Tamoxifens, and Vinblastines.