Copyright
©The Author(s) 2017.
World J Clin Oncol. Jun 10, 2017; 8(3): 241-248
Published online Jun 10, 2017. doi: 10.5306/wjco.v8.i3.241
Published online Jun 10, 2017. doi: 10.5306/wjco.v8.i3.241
Chemotherapeutic agent | Class | Mechanism of action | Cell cycle effect | Risk of infertility |
Cyclophosphamide | Alkylating agent | DNA cross-link formation and double strand breaks that result in inhibition of DNA function and synthesis leading to cellular apoptosis | Cell cycle non-specific | High risk |
Doxorubicin Epirubicin | Anthracyclines | Inhibition of DNA synthesis and function due to inactivation of DNA topoisomerase II, free oxygen radical formation and induction of DNA double-strand breaks | Cell cycle non-specific | Medium risk |
Carboplatin | Platinum analog | Inhibition of DNA synthesis and function via intra- and interstrand DNA cross-link formation by covalent binding to genome | Cell cycle non-specific | Medium risk |
Paclitaxel Docetaxel | Taxanes | Inhibition of mitotic division by binding to microtubules with enhancement of tubulin polymerization | M phase | Low risk |
Methotrexate | Antimetabolites | Inhibition de novo purine nucleotide synthesis by inactivation of dihydrofolate reductase | S phase | Low risk |
5-fluorouracil | Inhibition of DNA synthesis and function via inactivation of Thymidylate synthase and alteration in RNA processing | S phase | Low risk | |
Trastuzumab | Monoclonal antibodies | Blockage of Human epidermal growth factor receptor 2 subdomain IV, antibody dependent cellular toxicity | NA | Low or no risk |
Pertuzumab | Blockage of Human epidermal growth factor receptor 2 subdomain II, antibody dependent cellular toxicity |
- Citation: Taylan E, Oktay KH. Current state and controversies in fertility preservation in women with breast cancer. World J Clin Oncol 2017; 8(3): 241-248
- URL: https://www.wjgnet.com/2218-4333/full/v8/i3/241.htm
- DOI: https://dx.doi.org/10.5306/wjco.v8.i3.241