Proto-oncogens and Tumour suppressors Flashcards

1
Q

Tumour suppressors

A

inhibit cell cycle progression and often cause cell death or DNA repair

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2
Q

How can tumour suppressors cause cancer

A

when they become mutated

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3
Q

the 2 hit hypothesis and tumour suppressors

A

for loss of function both suppressor genes must be mutated

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4
Q

key tumour suppressors (6)

A

1) p53
2) APC
3) DCC
4) BRCA 1/2
5) Pten
6) Rb

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5
Q

p53 is involved with

A

the majority of cancers

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6
Q

Rb is involved with

A

retinoblastomas and osteogenic sarcomas

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7
Q

APC is involved with

A

colon

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8
Q

DCC is involved with

A

colon rectal

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9
Q

BRCA 1/2 is involved with

A

breast cancer and ovarian cancer

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10
Q

PTen is involved with

A

Gliomas , breast, thyroid

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11
Q

how does p53 act as a tumour suppressor

A

1) damaged DNA activates ATM
2) ATM activates Chk1/2 which phosphorylates p53
3) causes Mdm2 to unbind p53
4) p53 goes to nucleus and transcribes apoptotic proteins as well as P21 and p27

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12
Q

P21 and P27

A

cause cell cycle arrest –> DNA repair

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13
Q

How does Rb act as a tumour suppressor ?

A

when Rb is bound to E2F it prevents it from translocation tot the nucleus
- therefore cyclin E and CDK2 are not transcribed

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14
Q

when the Rb gene is mutated

A

oncogene- since it no longer prevents E2F from translocating to the nucleus

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15
Q

APC stands for

A

adenomatous polyposis coli

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16
Q

APC is part of

A

the B-catenin destruction complex

-acts by negatively regulating B-catenin 9 a cell growth factor)

17
Q

when Wnt isn’t bound

A

APC causes the ubiquitination and phosphorylation of B-catenin meaning it is sent to the proteasome and cannot transcribed cell growth genes

18
Q

Pten

A

Inhibits PIP3/Akt

-these usually promote cell proliferation and survival

19
Q

BRCA -1/2

A

Act as tumour suppressors by repairing DNA and causing cell death

20
Q

DCC is a tumour suppressor when

A

Netrin-1 isn’t bound- causes apoptosis by activating caspases

21
Q

Proto-oncogenes

A

encode different proteins which stimulate cell division, cell survival and inhibit differentiation

22
Q

porto-oncogenes mutate and become

A

oncogenes

23
Q

basic detail of how proto oncogenes can cause cancer

A

1) oncogene have a gain of function
2) uncontrolled cell division
3) tumour
4) cancer

24
Q

4 ways in which proto-oncogenes can mutate to oncogenes

A

1) deletion/ point mutation
2) regulatory mutation
3) gene amplification
4) chromosomal translocation

25
Q

deletion and point mutations

A

hyperactive proteins made in normal amounts

26
Q

2) regulatory mutation
3) gene amplification
4) chromosomal translocation

A

normal protein but greatly over expressed

27
Q

chromosomal translocation

A

hyperactive fusion protein

28
Q

oncogenes being therapeutic targets

A

targeting oncogenes with drugs which can inhibit their action will half uncontrollable cell growth, preventing tumour development

29
Q

Examples of proto-oncogenes

A

SMO, ``egfr,` raf, DCC, RAS

30
Q

SMO

A

smoothened; a proto-oncogene involved in Hh singalong that controls skin growth

31
Q

normal SMO

A

Hh binds to PTCH, allowing SMO to move to the cilium and activate GLI
- cell growth and development

32
Q

a mutated SMO

A

will have its signal on the whole time, causing constant activation of GLI- constant cell growth and development- uncontrollable forth and division

33
Q

EGFR (MAPK receptor)

A
  • when over expressed: colorectal, pancreatic and lung cancer
  • mutated: non-small cell lung cancer , glioblastoma
34
Q

RAF

A
  • melanoma
  • papillary thyroid cancer
  • colon cancer
35
Q

DCC as a proto-oncogene

A

if this receptor is mutated to be turned not he whole time without entrain, it become a proto-oncogene

36
Q

RAS

A
  • part of MAPK cascade
  • provides signal which leads to cell division

if RAS mutates –> GTP is constantly bound leading to ERK being constantly activated

37
Q

RAS and which cancer

A

-pancreatic, colon, papillary thyroid cancer, non small cell lung cancer