12. Biological basis of cancer treatment Flashcards

1
Q

How is cytotoxic chemotherapy generally administered?

A

IV

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2
Q

Recall the 6 types of non-targetted cytotoxic chemotherapy available

A
  1. Alkylating agents
  2. Pseudoalkylating agents
  3. Anthracyclines
  4. Topoisomerase inhibitors
  5. Vinca alkaloids and taxanes
  6. Antimetabolites
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3
Q

Recall the MOA of alkylating agents

A

Add alkyl groups to guanine residues in DNA, producing cross-linking and therefore preventing DNA unravelling for replication. Triggers apoptosis.

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4
Q

Recall an example of an alkylating agent

A

Chlorambucil

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5
Q

Recall the MOA of pseudo-alkylating agents

A

Adds platinum to guanine residues in DNA - this creates cross-links between strands and prevents uncoiling for replication –> apoptosis

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6
Q

Recall an example of a pseudo-alkylating agent

A

Cisplatin

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7
Q

Recall the 2 classes of antimetabolite cytotoxic chemotherapy

A
  1. Purine/pyrimidine analogues

2. Folate antagonists

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8
Q

Recall the MOA of purine/pyrimidine analogues as a cytotoxic chemotherapy

A

By masquerading as a base they inhibit DNA synthesis - breaks DNA strand –> apoptosis

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9
Q

Recall the MOA of folate antagonists as a cytotoxic chemotherapy

A

Inhibit dihydrofolate reductase, thus preventing nucleic acid production

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10
Q

Recall an example of an anti-folate drug

A

Methotrexate

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11
Q

Recall the MOA of anthracyclines as a cytotoxic chemotherapy

A

Intercalate between bases in DNA, producing free radicals and therefore causing damage to DNA and cell membrane

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12
Q

Recall an example of an anthracycline drug

A

Doxorubicin

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13
Q

Recall the MOA of vinca alkaloids as a cytotoxic chemotherapy

A

Inhibition of assembly of mitotic spindle

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14
Q

Recall the MOA of taxanes as a cytotoxic chemotherapy

A

Inhibition of disassembly of mitotic spindle

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15
Q

What is the normal function of topoisomerase?

A

DNA uncoiling: induces temporary strand breaks in the phosphodiester backbone to protect free ends of DNA from aberrant recombination events

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16
Q

Recall the MOA of topoisomerase inhibitors as a cytotoxic chemotherapy

A

They alter the binding of the topoisomerase complex to make breaks in phosphodiester backbone permanent

17
Q

Recall 3 possible mechanisms of resistance to chemotherapy

A
  1. DNA-repair mechanisms upregulated
  2. PARP excises faulty bases
  3. Cell effluxes cell via ABC transporters (ATP-binding cassette)
18
Q

Recall 2 classes of targeted chemotherapy

A
  1. Small molecule inhibitors

2. Monoclonal antibodies

19
Q

What type of malignancy are monoclonal antibody-based chemotherapies particularly effective against?

A

Blood malignancies

20
Q

Recall 3 advantages of small-molecule inhibitors as a chemotherapy

A
  1. Cheap
  2. Oral administration
  3. Can target TKs with no EC domain
21
Q

Recall 3 useful comparisons of the usefulness of monoclonal antibodies vs small molecule inhibitors

A
  1. Half life: much longer for Monoclonals
  2. Ability to target TKs without EC domains: only SMIs
  3. Cost: SMIs much cheaper
22
Q

Recall a disadvantage of monoclonal antibodies as a chemotherapy

A

Low penetration due to their bulky structure

23
Q

Recall a disadvantage of small molecule inhibitors as a chemotherapy

A

Unexpected toxicity due to pleiotropic targets

24
Q

Recall the MOA of small molecule inhibitors

A

They bind to the intracellular kinase of RPTKs leading to blockade of autophosphorylation and therefore downstream signalling

25
Q

Give an example of a small molecule inhibitor and its MOA

A

Glivec

Binds the ATP-binding region of the kinase domain of ABL1 - used to treat Philadelphia chromosome CML

26
Q

Recall the MOA of monoclonal antibodies as a chemotherapy

A

Bind the extracellualar domain of RPTKs, preventing dimerisation and leading to receptor endocytosis

27
Q

Recall a monoclonal antibody used in colorectal cancer

A

Bevacizumab - targets VEGF

28
Q

Recall 3 possible mechanisms of resistance to targeted chemotherapies

A
  1. Heterogeneity of tumour
  2. Mutation in ATP-binding region of RPTK
  3. Upregulation of a different proliferation pathway to divide despite drug
29
Q

Recall 2 genome-related chemotherapy options

A
  1. RNA interference

2. Anti-sense oligonucleotides

30
Q

What are anti-sense oligonucleotide therapies particularly useful for?

A

“undruggable” targets

31
Q

Recall 4 side effects that are common to most cytotoxic chemotherapies

A
  1. Alopecia
  2. Bone marrow suppression
  3. Fatigue
  4. Nausea and vomiting
32
Q

In which tissues are alkylating agents particularly toxic?

A

Kidneys, mouth, neurons

33
Q

In which tissues are anthracyclines particularly toxic?

A

Cardiac

34
Q

In which tissues are vinca alkaloids and taxanesparticularly toxic?

A

Nerves

35
Q

Recall 3 new therapeutic avenues being explored for cancer therapy

A
  1. Nanotherapy for cytotoxic drug delivery
  2. Immunotherapies
  3. Targeting cancer metabolism