Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Epigenetics ; 13(1): 95-107, 2018.
Article in English | MEDLINE | ID: mdl-29235922

ABSTRACT

Patterns of DNA methylation, an important epigenetic modification involved in gene silencing and development, are disrupted in cancer cells. Understanding the functional significance of aberrant methylation in tumors remains challenging, due in part to the lack of suitable tools to actively modify methylation patterns. DNA demethylation caused by mammalian DNA methyltransferase inhibitors is transient and replication-dependent, whereas that induced by TET enzymes involves oxidized 5mC derivatives that perform poorly understood regulatory functions. Unlike animals, plants possess enzymes that directly excise unoxidized 5mC from DNA, allowing restoration of unmethylated C through base excision repair. Here, we show that expression of Arabidopsis 5mC DNA glycosylase DEMETER (DME) in colon cancer cells demethylates and reactivates hypermethylated silenced loci. Interestingly, DME expression causes genome-wide changes that include both DNA methylation losses and gains, and partially restores the methylation pattern observed in normal tissue. Furthermore, such methylome reprogramming is accompanied by altered cell cycle responses and increased sensibility to anti-tumor drugs, decreased ability to form colonospheres, and tumor growth impairment in vivo. Our study shows that it is possible to reprogram a human cancer DNA methylome by expression of a plant DNA demethylase.


Subject(s)
Arabidopsis Proteins/genetics , Colonic Neoplasms/drug therapy , Colonic Neoplasms/genetics , DNA Methylation , N-Glycosyl Hydrolases/genetics , Trans-Activators/genetics , Animals , Antineoplastic Agents/pharmacology , Arabidopsis Proteins/metabolism , Cell Cycle/drug effects , Cell Cycle/genetics , Cell Line, Tumor , Colonic Neoplasms/pathology , DNA Repair/genetics , Fluorouracil/pharmacology , Gene Expression Regulation, Neoplastic , Genes, Tumor Suppressor , Genes, p16 , Humans , Mice, Nude , N-Glycosyl Hydrolases/metabolism , Oncogene Proteins/genetics , Oxaliplatin/pharmacology , Receptor Tyrosine Kinase-like Orphan Receptors/genetics , Trans-Activators/metabolism , Transgenes , Xenograft Model Antitumor Assays
SELECTION OF CITATIONS
SEARCH DETAIL
...