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Pharmacology

Microtubule inhibitors, anthracyclines and topoisomerase inhibitors

How vinca alkaloids and taxanes disrupt the mitotic spindle, how topoisomerase poisons turn transient DNA breaks into lethal ones, why irinotecan toxicity depends on UGT1A1, and how anthracycline cardiotoxicity relates to cumulative dose and is monitored under the ESC cardio-oncology guideline.

Tier 2Medical sciences concept

Written with AI assistance and fact-checked against the sources below. For exam study, not clinical decisions. How notes are made

3 questions9 flashcards

At a glance

  • Microtubule inhibitors (vinca alkaloids, taxanes, eribulin) disrupt the mitotic spindle and arrest cells in M phase. Microtubules also carry axonal transport, so peripheral neuropathy is the class toxicity.
  • Topoisomerase poisons trap the enzyme on DNA after it has cut. Topoisomerase I inhibitors leave single-strand breaks; topoisomerase II inhibitors leave double-strand breaks.
  • Anthracyclines intercalate into DNA, poison topoisomerase II and generate iron-dependent free radicals. Cumulative dose-dependent cardiomyopathy is the exam topic.

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Last updated
14 November 2026
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