MCB Lecture 29 Cancer treatment Flashcards

0
Q

Describe what is meant by targeted therapy

A

Only the mutated driver is targeted. Thus, normal versions are not adversely affected

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1
Q

What are the two standard therapeutic approaches?

A
  1. Block cofactor site of an enzyme

2. Antibody binds to the receptor, or to the ligand so that there can be no intracellular response

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2
Q

Describe therapy in CML

A

CML is caused by bra-abl on Philadelphia chromosome
This codes for a constitutive lay active tyrosine kinase, which activates STAT5
STAT5 leads to proliferation of hematopoetic cells

By blocking the ATP binding site in the tyrosine kinase, we don’t get phosphorylated STAT5, and thus no proliferation

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3
Q

What does Imatinib do?

A

Imatinib blocks the ATP site in the brc-abl tyrosine kinase

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4
Q

Describe how genetics is important in targeted therapy

A

Not all forms of the cancer will have the same mutations

We need to do genetic screens to see if a person has a mutation to see if the targeted therapy will be any help

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5
Q

Describe therapy in melanoma

A

Half of melanomas have a mutation in BRAF

By targeting BRAF, we stop the pathway that leads to cell growth and proliferation

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6
Q

What does vemurafenib do?

A

Vermurafenib blocks the mutated form of BRAF, thus preventing cell proliferation

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7
Q

Describe the problem of acquired resistance

A

Compounds further down the pathway mutate, and thus we get tumour growth again

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8
Q

Describe the change in survival time with targeted therapies

A

Targeted therapies increase the survival time

However, after a certain amount of time, the cancer comes back and the patient dies

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9
Q

What is being done to improve acquired resistance

A

Compound treatments: target all the drivers at once so there can be no evolution of resistance

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10
Q

Describe why personal genomics is important for cancer treatment

A

This is because we need to see which particular mutations an individual has so that we get them the best treatment

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11
Q

Explain gene therapy

A

Recombinant DNA put into a patient (virus, vector) to replace the mutated or defective DNA

This has n,y had marginal success

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