Antimetabolites Flashcards

1
Q

What is the way that Antimetabolites work within the body to affect cancer?

A
  • Block the production of one or more of these building block [nucleotides] = DECREASE in DNA replication and transcription
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2
Q

What is the main part of the cell cycle that Antimetabolites affect?

A
  • S Phase = Inhibit Synthesis
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3
Q

What are the Pyridine Analongs?

A
  • 5-FU, Capecitabine [nucleotide production]
  • Ara-C, Gemcitabine [DNA polymerase]
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4
Q

What is the mechanism of action for 5-Fluorouracil [5-FU]?

A
  • Will INHIBIT thymidine synthesis for dUMP to TMP = inhibition of DNA synthesis
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5
Q

What is the way that 5-FU stops the production of TMP & the DNA replication?

A
  • 5-FU makes fdUMP [mimincs dUMP]
  • Tetrahydofolate binds to fdUMP locking [F- group] it in Ternary Complex = thymineless death
  • Tymidylate Synthase can’t break the FdUMP
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6
Q

What is the importance of Thymidylate Synthase?

A
  • Makes TMP from dUMP = DNA proliferation
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7
Q

How does 5-FU interfere with RNA produce?

A
  • 5-FU makes FdUTP [mimics UTP] causing RNA death
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8
Q

What are some of the ways that 5-FU is resisted in the body?

A
  • By dowregulation of enzymes [NO 5-FU to FdUMP]
  • Upregulation of Thymidylate Synthease [increase TMP production]
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9
Q

How would toxicites arise in patients taking 5-FU for cancer treatment?

A
  • Polymorphism: deficiency of dihydropyrimidine dehydrogenase [DPD] which breaks down 5-FU; decrease DPD = increase 5-FU = more toxicities
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10
Q

What is one way that Thymidine will help with 5-FU?

A
  • Thymidine THEN 5-FU: more thymidine affecting thymidine synthesis = increased efficacy for 5-FU
  • 5-FU THEN Thymidine: Helps with Overdose
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11
Q

What is Leucovorate and how does Leucovorate help 5-FU?

A
  • Leucovorate is basically folate
  • It helps by over saturating the folate site and make more tetrahydrofolate = increase efficacy of 5-FU
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12
Q

What is the mechanism of action for Capecitabine?

A
  • Will INHIBIT thymidine synthesis [same and 5-FU]
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13
Q

What is important to know about Capecitabine?:

A
  • Orally active prodrug = improves selectivity to tumors while decreasing toxicities
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14
Q

What is the mechanism of action for Cytarabine?

A
  • Inihibit DNA polymerase = Decreasing DNA replication
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15
Q

In what way does Cytarabine inhibit DNA polymerase?

A
  • Its converted to Ara-C causing the inhibition
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16
Q

What is the way that Cytarabine can be toxic and where does it affect?

A
  • Cytidine Deaminase converts cytarabine to Ara-C
  • DECREASE cytidine Deaminase will make Cytidine VERY toxic in CNS = leukemia and lymphoma
17
Q

What are some of the ways that Cytarabine has resistance?

A
  • Downregulation of enzyme [NO Ara-C made]
  • Upregulation of Cytidine Deaminase [lower Ara-C]
  • Downregulation of transporters [NO drug in cell]
18
Q

What is the mechanism of action for gemcitabine?

A
  • Inhibit DNA polymerase [same as Cytarabine]
19
Q

What is important to know about the potency of Gemcitabine?

A
  • Has greater potency than Cytarabine
20
Q

What is the way that Terahydrouridine is used to help Cytarabine?

A
  • Cytidine Deaminase Inhibitor = INCREASED levels of Ara-C [may increase Toxicity]
21
Q

What are the Purine Analogs?

A
  • 6-Mercaptopurine, 6-Thioguanine
22
Q

What is the mechanism of action for 6-Mercaptopurine?

A
  • Inhibits purine nucleotide production [MULTIPLE enzymes]
  • Converted to TIMP via HGPRT [active]
23
Q

What is one way that 6-MP could become toxic within the body?

A
  • Polymorphism: TPMT inactivates 6-MP
  • Decrease in TMPT will increase hematologic toxicities [lower bone marrow and blood cells]; drugs isnt metabolized quickly
24
Q

What is the way that Allopurinol affects 6-MP?

A
  • Allopurinol is a Xanthine Oxidase inhibitor; Xanthine Oxidase breaks down 6-MP; Allopurinol will increase 6-MP toxicities
25
Q

What is the mechanism of action for 6-Thioguanine?

A
  • Inhibit purine nucleotide production [same as 6-mercapopurine]
26
Q

What is important to know about 6-thioguanine and allopurinol?

A
  • DOES NOT break down 6-TG
27
Q

What is folate?

A
  • B9
  • Needed for Metabolism of Amino Acids and nucleic acids
  • FH2 to FH4
  • Methly donor for MTHF
28
Q

Brief explain the Folic Acid Cycle?

A
  • Folate enters as Dihydrofolate [FH2]
  • FH2 reduce to Tetrahydrofolate [FH4] by dihydrofolate reductase [DHFR]
  • MTHF converted to FH2 where it helps make TMP from dUMP
29
Q

What happen when Dihydrofolate Reductase [DHFR] become inhibited?

A
  • Cause an increase in FH2 [inactive] causing an INHIBITION in Thymidine Synthesis = decrease TMP
30
Q

What is the mechanism of action for Methotrexate?

A
  • Inhibits DHFR = lower THF levels causing a decrease in DNA synthesis
31
Q

What would be a way that there is resistance for Methotrexate?

A
  • Amplification of DHFR
  • Mutation of DHFR to resistant the enzyme
32
Q

What is Leucovorin and how does it help against overdose?

A
  • Basically folate
  • Used to reverse overdose of MTX toxicity by INCREASING tetrahydrofolate and REVERSE toxic effects of DHFR inhibition
33
Q

How does Lecovorin compare to Lecovorate?

A
  • Lecovorin helps with MTX = DECREASE efficacy
  • Lecovorate helps with 5-FU = INCREASE efficacy
34
Q

What rescues a 5-FU overdose?

A
  • Thymidine
35
Q

Which antifolate inhibits multiple enzymes, which results in decreased resistance?

A
  • Pemetrexed
36
Q

Which antimetabolite should not be given to patents being treated for gout?

A
  • 6-MP
37
Q
A