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Biochemistry · Nucleotide drugs: cytarabine
Sample itemA 35-year-old with acute myeloid leukaemia receives cytarabine in induction chemotherapy. Which statement best describes its action?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. It is phosphorylated by deoxycytidine kinase to ara-CTP, which competes with dCTP and inhibits DNA polymerase in S phase
Cytarabine is a cytidine analogue with arabinose in place of ribose. It enters cells, is phosphorylated by deoxycytidine kinase to ara-CTP, which is incorporated into DNA and inhibits DNA polymerase, so it is S-phase specific. Cerebellar toxicity and myelosuppression are important adverse effects.
Option by option
A. It inhibits IMP dehydrogenase and depletes guanine nucleotides
IMP dehydrogenase inhibition is the action of mycophenolate.
B. It is phosphorylated by deoxycytidine kinase to ara-CTP, which competes with dCTP and inhibits DNA polymerase in S phase (correct)
Ara-CTP competes with dCTP and blocks DNA chain elongation in S-phase cells.
C. It is converted to FdUMP and inhibits thymidylate synthase
FdUMP formation and thymidylate synthase inhibition describes fluorouracil.
D. It inhibits dihydrofolate reductase and depletes tetrahydrofolate
Dihydrofolate reductase inhibition is the action of methotrexate.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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