|
DNA Damaging Drugs
The first drugs developed for the treatment of cancer in the
1940's were DNA damaging agents (nitrogen mustards). In order
to divide rapidly, cancer cells must duplicate their DNA efficiently
in order to create two viable daughter cells. The DNA is duplicated
in the S-phase of the cell cycle. If the DNA is damaged by radiation
or an anticancer drug, the cell will be forced to stop growing
(growth arrest) and decide how to handle the DNA damage. Repairing
the DNA is one action that may enable cancer cells to resist
the cytotoxic effects of DNA damaging agents. However, if the
level of damage is too high or the cell cannot efficiently repair
the damage, then cell death is likely to occur.
There are a variety of DNA damaging agents (see below). Each
drug differs in the type of damage that it forms with DNA and
the relative cytotoxic effect each has on different types of
cancer cells. In other words, some tumors are more sensitive
to certain agents than others. Over the years, many clinical
trials have been conducted to determine which agents are most
effective in treating which tumor types. For more information
on each drug, please click on the link for each drug below.
Nitrogen mustards (Mustargen, Cyclophosphamide, Ifosfamide,
Melphalan, Chlorambucil)
Aziridines and Epoxides (Thiotepa, Mitomycin C)
Alkyl Sulfonates (Busulfan)
Nitrosoureas (BCNU-carmustine)
Hydrazine and Triazines (Procarbazine, Dacarbazine, Temozolomide)
Platinum Drugs (Cisplatin, Carboplatin, Oxaliplatin)
|