Frequent inactivation of cysteine dioxygenase type 1 contributes to survival of breast cancer cells and resistance to anthracyclines.

Jeschke, Jana; O'Hagan, Heather M; Zhang, Wei; Vatapalli, Rajita; Calmon, Marilia Freitas; Danilova, Ludmila; Nelkenbrecher, Claudia; Van Neste, Leander; Bijsmans, Ingrid IT; van Engeland, Manon; Gabrielson, Edward; Schuebel, Kornel K.E.; Winterpacht, Andreas; Baylin, Stephen B; Herman, James G; Ahuja, Nita

doi:doi/10.1158/1078-0432.CCR-12-3751

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Frequent inactivation of cysteine dioxygenase type 1 contributes to survival of breast cancer cells and resistance to anthracyclines.

par Jeschke, Jana

;O'Hagan, Heather M ;Zhang, Wei ;Vatapalli, Rajita ;Calmon, Marilia Freitas ;Danilova, Ludmila ;Nelkenbrecher, Claudia ;Van Neste, Leander ;Bijsmans, Ingrid IT ;van Engeland, Manon ;Gabrielson, Edward ;Schuebel, Kornel K.E.;Winterpacht, Andreas ;Baylin, Stephen B ;Herman, James G ;Ahuja, Nita
Référence Clinical cancer research, 19, 12, page (3201-3211)
Publication Publié, 2013-06

Article révisé par les pairs

Résumé :

Genome-wide DNA methylation analyses have identified hundreds of candidate DNA-hypermethylated genes in cancer. Comprehensive functional analyses provide an understanding of the biologic significance of this vast amount of DNA methylation data that may allow the determination of key epigenetic events associated with tumorigenesis.

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