Cancer is generally defined as the uncontrolled growth of abnormal cells in the body. One of the common approaches in treatment of cancer is to use drugs that target fast-dividing cells at different phases of the cell cycle. This pharmacology lecture covers mechanism of action and side effects of cell cycle specifc agents including topoisomerase inhibitors (type I & type II) and microtubule inhibitors (vinca alkaloids & taxanes) as well as cell cycle nonspecfic agents including antitumor antibiotics (anthracyclines), alkylating agents (nitrogen mustards, nitrosoureas, triazines, alkyl sulfonates), platinum coordination complexes, tyrosine kinase inhibitors (targeting BCR-ABL, HER2, PDGF, VEGF, EGF receptors), and monoclonal antibodies. Antineoplastic drugs mentioned include; Irinotecan, Topotecan, Etoposide, Vincristine, Vinblastine, Vinorelbine, Paclitaxel, Docetaxel, Cabazitaxel, Doxorubicin, Daunorubicin, Epirubicin, Idarubicin, Bleomycin, Chlorambucil, Cyclophosphamide, Ifosfamide, Melphalan, Carmustine, Lomustine, Dacarbazine, Temozolomide, Busulfan, Cisplatin, Carboplatin, Oxaliplatin, Imatinib, Dasatinib, Nilotinib, Lapatinib, Sunitinib, Erlotinib, Trastuzumab, Cetuximab, Bevacizumab, and Rituximab.
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Source of image beginning at 5:36 showing one-electron redox cycle of anthracyclines:
Source of image beginning at 7:57 showing Cisplatin activation and DNA damage induction:
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