Response and toxicity to cytarabine therapy in leukemia and lymphoma: from dose puzzle to pharmacogenomic biomarkers

R Di Francia, S Crisci, A De Monaco, C Cafiero, A Re… - Cancers, 2021 - mdpi.com
Simple Summary In this review, the authors propose a crosswise examination of cytarabine-
related issues ranging from the spectrum of clinical activity and severe toxicities, through …

Genetic factors influencing cytarabine therapy

JK Lamba - Pharmacogenomics, 2009 - Taylor & Francis
The mainstay of acute myeloid leukemia chemotherapy is the nucleoside analog cytarabine
(ara-C). Numerous studies suggest that the intracellular concentrations of the ara-C active …

ABC transporters and their role in nucleoside and nucleotide drug resistance

Y Fukuda, JD Schuetz - Biochemical pharmacology, 2012 - Elsevier
ATP-binding cassette (ABC) transporters confer drug resistance against a wide range of
chemotherapeutic agents, including nucleoside and nucleotide based drugs. While …

Immunohistochemical and genetic evaluation of deoxycytidine kinase in pancreatic cancer: relationship to molecular mechanisms of gemcitabine resistance and …

V Sebastiani, F Ricci, B Rubio-Viquiera, P Kulesza… - Clinical Cancer …, 2006 - AACR
Gemcitabine is considered the standard first-line therapy for patients with advanced
pancreatic cancer. More recent strategies have focused on improving the efficacy of …

The human equilibrative nucleoside transporter 1 mediates in vitro cytarabine sensitivity in childhood acute myeloid leukaemia

I Hubeek, RW Stam, GJ Peters, R Broekhuizen… - British journal of …, 2005 - nature.com
Cytarabine (ara-C) is the most effective agent for the treatment of acute myeloid leukaemia
(AML). Aberrant expression of enzymes involved in the transport/metabolism of ara-C could …

Review of recent studies on resistance to cytotoxic deoxynucleoside analogues

LP Jordheim, C Dumontet - Biochimica et Biophysica Acta (BBA)-Reviews …, 2007 - Elsevier
Cytotoxic deoxynucleoside analogues are widely used in the treatment of haematological
malignancies and solid tumours. Their metabolism and mechanisms of action are relatively …

[HTML][HTML] Gemcitabine uptake in glioblastoma multiforme: potential as a radiosensitizer

J Sigmond, RJ Honeywell, TJ Postma, CMF Dirven… - Annals of oncology, 2009 - Elsevier
Glioblastoma multiforme (GBM), the most frequent malignant brain tumor, has a poor
prognosis, but is relatively sensitive to radiation. Both gemcitabine and its metabolite …

The clinically relevant pharmacogenomic changes in acute myelogenous leukemia

A Emadi, JE Karp - Pharmacogenomics, 2012 - Taylor & Francis
Acute myelogenous leukemia (AML) is an extremely heterogeneous neoplasm with several
clinical, pathological, genetic and molecular subtypes. Combinations of various doses and …

The role of l-leucovorin uptake and metabolism in the modulation of 5-fluorouracil efficacy and antifolate toxicity

GJ Peters, I Kathmann, E Giovannetti, K Smid… - Frontiers in …, 2024 - frontiersin.org
Background L-Leucovorin (l-LV; 5-formyltetrahydrofolate, folinic acid) is a precursor for 5, 10-
methylenetetrahydrofolate (5, 10-CH2-THF), which is important for the potentiation of the …

Carboranyl thymidine analogues for neutron capture therapy

W Tjarks, R Tiwari, Y Byun, S Narayanasamy… - Chemical …, 2007 - pubs.rsc.org
Neutron capture therapy (NCT) is a binary radio-chemotherapeutic modality for the treatment
of cancer. A major focus of NCT-related research is the development of novel tumor …