Point mutations in human guanylate kinase account for acquired resistance to anticancer nucleotide analogue PMEG

Helena Mertlíková-Kaiserová (1) , Michaela Rumlová (1) , Eva Tloušťová (1) , Eliška Procházková (1) , Antonín Holý (1) , Ivan Votruba (1)

1 CAS - Czech Academy of Sciences [Prague]

Acyclic nucleotide analogue PMEG represents promising drug candidate against lymphomas. In the present work we describe the ability of PMEG to induce resistance and we elucidate the mechanisms involved in this process. CCRF-CEM T-lymphoblastic cells resistant to either PMEG or its 6-amino congener PMEDAP were prepared and assayed for the expression of membrane transporters, PMEG and PMEDAP uptake and intracellular metabolism. Genes for guanylate kinase (GUK) and adenylate kinase (AK) isolated from PMEG- and PMEDAP-resistant cells were sequenced and cloned into mammalian expression vectors. PMEG-resistant cells were transfected with GUK vectors and catalytic activities of GUKs isolated from PMEG-sensitive and resistant cells were compared. PMEG phosphorylation to PMEG mono- and diphosphate was completely impaired in resistant cells. GUK obtained from PMEG-resistant cells revealed two point mutations SN VF that significantly suppressed its catalytic activity. Transfection of resistant cells with wtGUK led to the recovery of phosphorylating activity as well as sensitivity towards PMEG cytotoxicity. No differences in PMEG uptake have been found between sensitive and resistant cells. In contrast to GUK no changes in primary sequence of AK isolated from PMEDAP resistant cells were identified. Therefore, resistance induced by PMEDAP appears to be conferred by other mechanisms. In conclusion, we have identified GUK as the sole molecular target for the development of acquired resistance to the cytotoxic nucleotide PMEG. Therefore, PMEG is unlikely to cause cross-resistance in combination therapeutic protocols with most other commonly used anticancer drugs.

Mots clés: Resistance; acyclic nucleoside phosphonates; PMEG; PMEDAP; guanylate kinase; adenylate kinase

Domaines: Pharmacologie

Helena Mertlíková-Kaiserová, Michaela Rumlová, Eva Tloušťová, Eliška Procházková, Antonín Holý, et al.. Point mutations in human guanylate kinase account for acquired resistance to anticancer nucleotide analogue PMEG. Biochemical Pharmacology, 2011, ⟨10.1016/j.bcp.2011.04.002⟩. ⟨hal-00703550⟩