Alkylating antineoplastic agent

An alkylating antineoplastic agent is an alkylating agent that attaches an alkyl group to DNA.

Since cancer cells generally proliferate unrestrictively more than do healthy cells they are more sensitive to DNA damage, and alkylating agents are used clinically to treat a variety of tumours.

Additional recommended knowledge

Better weighing performance in 6 easy steps

Daily Visual Balance Check

What is the Sensitivity of my Balance?

Agents acting nonspecifically

Some alkylating agents are active under conditions present in cells; and the same mechanism that makes them toxic allows them to be used as anti-cancer drugs. They stop tumour growth by cross-linking guanine nucleobases in DNA double-helix strands - directly attacking DNA. This makes the strands unable to uncoil and separate. As this is necessary in DNA replication, the cells can no longer divide. These drugs act nonspecifically.

Agents require activation

Some of them require conversion into active substances in vivo (e.g. cyclophosphamide).

Cyclophosphamide is one of the most potent immunosuppressive substances. In small dosages, it is very efficient in the therapy of systemic lupus erythematosus, autoimmune hemolytic anemias, Wegener's granulomatosis and other autoimmune diseases. High dosages cause pancytopenia and hemorrhagic cystitis.

Dialkylating agents, limpet attachment, and monoalkylating agents

Dialkylating agents can react with two different 7-N-guanine residues and if these are in different strands of DNA the result is cross-linkage of the DNA strands, which prevents uncoiling of the DNA double helix. If the two guanine residues are in the same strand the result is called limpet attachment of the drug molecule to the DNA.

Monoalkylating agents can react only with one 7-N of guanine.

Limpet attachment and monoalkylation do not prevent the separation of the two DNA strands of the double helix but do prevent vital DNA processing enzymes from accessing the DNA. The final result is inhibition of cell growth or stimulation of apoptosis, cell suicide.

Examples

In the Anatomical Therapeutic Chemical Classification System, alkylating agents are classified under L01A.

Alkylating agents activated by cytochrome p-450:

• Alkyl sulfonates
  • Busulfan (L01AB01)
• Ethyleneimines and methylmelamines
  • Hexamethylmelamine or altretamine (L01XX03)
  • Thiotepa (L01AC01)
• Nitrogen mustards
  • Cyclophosphamide (L01AA01)
  • Mechlorethamine or mustine (L01AA05)
  • Uramustine or uracil mustard (no ATC code, PubChem 6194, DrugBank APRD00130)
  • Melphalan (L01AA03)
  • Chlorambucil (L01AA02)
  • Ifosfamide (L01AA06)
• Nitrosoureas
  • Carmustine (L01AD01)
  • Streptozocin (L01AD04)
• Triazenes
  • Dacarbazine (L01AX04)
• Imidazotetrazines
  • Temozolomide (L01AX03)

Other selected examples: