3.5 cancer 2 Flashcards

1
Q

What are the two categories of tumor suppressor genes?

A
  1. proteins that normally restrict cell growth. 2. proteins that maintain integrity of the genome
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2
Q

Which of the two type of tumor suppressor gene categories is associated with AT

A

proteins that maintain integrity of the genome

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3
Q

What genes are associated with retinoblastoma?

A

tumor suppressor genes

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4
Q

What are the 2 forms of retinoblastoma?

A

Hereditary and sporadic

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5
Q

What % are hereditary and sporadic?

A

40% familial and 60% sporadic

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6
Q

Hereditary and sporadic affect how many eyes?

A

Hereditary effects both and sporadic affects one.

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7
Q

How does hereditary form Rb?

A

People only have one good copy of Rb gene and they loss or it gets deleted in every cell.

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8
Q

How many mutations need to happen in both hereditary and sporadic to form Rb?

A

familial needs 1 and sporadic needs 2.

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9
Q

What 4 things is p53 involved in?

A

cell cycle arrest, dna repair, apoptosis, and block of angiogenesis.

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10
Q

In what two ways is p53 a gene regulatory protein?

A

Stimulates transcription of p21. Also activates pro apoptotic proteins BH123 and BH-3 only

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11
Q

Where does colorectal cancer arise?

A

Epithelial lining of large intestine.

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12
Q

What is a precursor for colorectal cancer?

A

Polyp

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13
Q

What two mutations cause colorectal cancers?

A

40% point mutation in K-Ras and 60% inactivating mutation of p53.

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14
Q

What is an important mutation for colorectal cancer?

A

Apc mutation

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15
Q

Patients with FAP have what?

A

inactivating mutations or deletion of one copy of Apc

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16
Q

how does chemotherapy cure cancer?

A

Stops cell division.

17
Q

What are the issues with chemotherapy?

A

Stops rapid dividing cells in the whole body like hair cells, stomach, blood cells. Thus loss of hair, nausea, anemia.

18
Q

What is responsible for CML?

A

philadelphia chromosome. Translocation between chrom 9 and 22.

19
Q

What is abl?

A

Tyrosine kinase for cell signaling

20
Q

How does Bcr-abl form?

A

Chromosomal translocation

21
Q

What does Bcr-abl do?

A

Cell proliferation, CML

22
Q

How do you treat CML?

A

gleevac

23
Q

How are oncogenes activated?*

A

Gene amplification, chromosome rearrangement, regulatory mutation. point mutation.

24
Q

What is the dif between benign and malignant tumor?**

A

Benign tumor doesn’t move but a malignant tumor has the ability to invade surrounding tissues.

25
Q

Why is colon cancer one of the most treatable cancers?**

A

Slow disease progression. Polyp is a precursor to cancer. Cut polyp and its a cure.

26
Q

How does Gleevac work?

A

Gleevec takes the place of ATP on Bcr-Abl. Substrate not changed.