Antifolates are a class ofantimetabolite medications that antagonise (that is, block) the actions offolic acid (vitamin B9).[1] Folic acid's primary function in the body is as a cofactor to various methyltransferases involved in serine, methionine, thymidine and purine biosynthesis. Consequently, antifolates inhibit cell division, DNA/RNA synthesis and repair and protein synthesis. Some such as proguanil, pyrimethamine and trimethoprim selectively inhibit folate's actions in microbial organisms such as bacteria, protozoa and fungi. The majority of antifolates work by inhibitingdihydrofolate reductase (DHFR).[2]
| Drug | Class | Pharmacologic target | Myelosuppressive effect | US pregnancy category | Indications | Notable adverse effects |
|---|---|---|---|---|---|---|
| Methotrexate[3] | Antineoplastic & immunosuppressant | Mammalian DHFR | +++ | X | Malignancies (esp. haematologic malignancies andosteosarcoma), ectopic pregnancy and autoimmune conditions (esp.rheumatoid arthritis,psoriasis,Granulomatosis with polyangiitis,Goodpasture syndrome, etc.) | Kidney or liver failure,Stevens–Johnson syndrome,toxic epidermal necrolysis, infection, aplastic anaemia, opportunistic infections and GI effects. |
| Pemetrexed[4] | Antineoplastic | Mammalian DHFR, TS, GARFT | +++ | D | Non-small cell lung carcinoma &mesothelioma | Nausea, vomiting, dyspnoea, constipation, chest pain, diarrhoea, weight loss,stomatitis, rash, fever, peripheral neuropathy, dehydration, kidney failure, Stevens–Johnson syndrome, toxic epidermal necrolysis and erythema multiforme. |
| Proguanil[5] | Antimalarial | Protozoal DHFR | +/- | C | Malaria, prevention and treatment | Abdominal pain, headaches, increased LFTs, myalgia, nausea, opportunistic infections, diarrhoea, vomiting, etc. Less commonly Stevens–Johnson syndrome, toxic epidermal necrolysis, agranulocytosis, liver failure, anaphylaxis, etc. |
| Pyrimethamine[6] | Antiprotozoal | Protozoal DHFR | +/- | C | Malaria, toxoplasmosis and pneumocystis jiroveci pneumonia. | Stevens–Johnson syndrome, toxic epidermal necrolysis, agranulocytosis and aplastic anaemia. |
| Trimethoprim[7] | Broad-spectrum antimicrobial | Microbial DHFR | +/- | C | Numerous (especially when in combination with the sulfonamide, sulfamethoxazole); treatment & prophylaxis forpneumocystis jiroveci pneumonia,malaria andtoxoplasmosis. Treatment ofmelioidosis,shigellosis,listeria,urinary tract infections, acute infectious exacerbations ofchronic bronchitis, infection prophylaxis in HIV-positive individuals, cyclospora protozoa, etc. | Stevens–Johnson syndrome, toxic epidermal necrolysis, agranulocytosis and aplastic anaemia. |
Many are primarily DHFR inhibitors, but raltitrexed is an inhibitor of thymidylate synthase, and pemetrexed inhibits both and a third enzyme.
Antifolates act specifically during DNA and RNA synthesis, and thus are cytotoxic during the S-phase of the cell cycle. Thus, they have a greater toxic effect on rapidly dividing cells (such as malignant and myeloid cells, and GI & oral mucosa), which replicate their DNA more frequently, and thus inhibits the growth and proliferation of these non-cancerous cells as well as causing the side-effects listed.
The antifolate action specifically targets the fast-dividing cells, and tend to have adverse effects on thebone marrow,skin, andhair. Asfolate is vital in the first trimester of pregnancy for healthy fetal development, the use of antifolates is strongly contraindicated in pregnancy and carries significantteratogenic risk.
Low doses of methotrexate can deplete folate stores and cause side-effects that are similar tofolate deficiency. Both high-folate diets and supplemental folic acid may help reduce the toxic side-effects of low-dose methotrexate without decreasing its effectiveness.[8][9]Anyone taking low-dose methotrexate for the health problems listed above should consult with a physician about the need for a folic acid supplement.
While the role of folate as a cancer treatment is well established, its long-term effectiveness is diminished by cellular response. In response to decreased tetrahydrofolate (THF), the cell begins to transcribe more DHF reductase, the enzyme that reduces DHF to THF. Because methotrexate is acompetitive inhibitor of DHF reductase, increased concentrations of DHF reductase can overcome the drugs inhibition.
Many new drugs are under development to reduce antifolatedrug resistance.[10][11]
The nameantifolate usually refers to drugs whose folate antagonism is intentional. In contrast, there are some other drugs, of severaldrug classes, that antagonize folate incidentally, as anadverse effect, whether mildly or heavily. This effect is often not noticeable except when it causes aneural tube defect in a fetus carried by a woman taking the medication. Such drugs include someanticonvulsants (valproic acid,carbamazepine,phenobarbital,phenytoin, andprimidone) andtrimethoprim.Lamotrigine is also an anticonvulsant with known (fromin vitro testing) weak anti-folate effects.[12] Many of these, or metabolites thereof, seem to mimick the default aromatic ring moiety of folic acid (-N=C(NH2)-NH-CO-C(R)=), especially lamotrigine and trimethoprim that share sequence (-N=C(NH2)-N=C(NH2)-C(R)=) with methotrexate, in which it is the primary modification to the folic acid structure.
