Estamos realizando la búsqueda. Por favor, espere...


Fludarabine resistance mediated by aminoglycoside-39- phosphotransferase-IIa and the structurally related eukaryotic cAMP-dependent protein kinase

Abstract: While working with G418-resistant stably transfected cells, we realized the neomycin resistance gene (NeoR), which encodes the aminoglycoside-39-phosphotransferase-IIa [APH(39)-IIa], also confers resistance to the nucleoside analog fludarabine. Fludarabine is a cytostatic drug widely used in the treatment of hematologic and solid tumors as well as in the conditioning of patients before transplantation of hematopoietic progenitors. We present evidence thatNeoR-transfected cells do not incorporate fludarabine, thus avoidingDNAdamage caused by the drug, evidenced by a lack of FANCD2 monoubiquitination and impaired apoptosis. A screening of other nucleoside analogs revealed that APH(39)-IIa only protects against ATP purine analogs. Moreover, APH(39)-IIa ATPase activity is inhibited by fludarabine monophosphate, suggesting that APH(39)-IIa blocks fludarabine incorporation intoDNAby dephosphorylating its active fludarabine triphosphate form. Furthermore, overexpression of the catalytic subunit of the eukaryotic kinase PKA,which is structurally related to APHs, also provides resistance to fludarabine, anticipating its putative utility as a response marker to the drug. Our results preclude the use of Neo marker plasmids in the study of purine analogs and unveils a new resistance mechanism against these chemotherapeuticals.?S´anchez-Carrera, D., Bravo-Navas, S., Cabez´on, E., Arechaga, I., Cabezas, M., Y´añez, L., Pipa´on, C. Fludarabine resistance mediated by aminoglycoside-39-phosphotransferase-IIa and the structurally related eukaryotic cAMP-dependent protein kinase.

Otras publicaciones de la misma revista o congreso con autores/as de la Universidad de Cantabria

 Fuente: FASEB J. 2017 Jul;31(7):3007-3017

Editorial: Federation of American Society of Experimental Biology (FASEB)

 Fecha de publicación: 01/07/2017

Nº de páginas: 16

Tipo de publicación: Artículo de Revista

 DOI: 10.1096/fj.201601245R

ISSN: 0892-6638,1530-6860