T2- MISC Flashcards
1
Q
increase susceptibility to UV damage
A
loss of NER
2
Q
increase metastasis
A
- loss of KAI1
- loss of E-cadherin
3
Q
decrease metastasis
A
- NM23
- CD44 involved with cell adhesion
- CD82 induced by p53
4
Q
anti-apoptosis
A
- decreased cytochrome c release from mitochondria:
a) Bcl2–> blocks channels made by BAX/BAK dimers
b) Bcl-xl–> binds to BAX/BAK to prevent their self association - decrease caspase activation–> XIAP: ubiquitination of capsize 3
- promotes cell survival
- AKT (PKB) when over activated in cancer cells contributes to decreased apoptosis.
5
Q
pro-apoptosis
A
- activation of cytochrome c with APAF1
- increase cytochrome c release from mitochondria
- dimerization of bax and bak.
- TRADD activation
- mitochondrial release of SMAC by bid
- SNAIL stabilizes AIF to expand its half life and promote apoptosis
- activation of MOAP1 promotes apoptosis of BAX
- endonuclease G is a caspace-independent apoptosis
- BAD is a pro-apoptotic unless phosphorylated by AKT
- BID is pro-apoptotic and activated BAX and BAK
- TRAIL activated apoptotic signal
- PUMA promoted apoptosis and is unregulated by p53
- BAX activated by p53 to promote apoptosis
6
Q
increases transcription
A
- LMP1 increases transcription bcl-2
- EBNA-2 increases transcription cyclin D
- STAT5 increases transcription e-cadherin
- E2F-DP1 increases transcription for S phase proteins
- Nf-kB increases transcription for inflammation and cell growth
- MYC when bound to MAX promotes transcription
- twist promotes transcription of n-cadherin
7
Q
decreases transcription
A
- SNAIL inhibits transcription of E-cadherin
- MAD when bound to MAX inhibits transcription
- GROUCHO bind TGF and is involved inhibiting TCF4 transcription
8
Q
increases ubiquitination (tagged for degradation) of p53
A
- HPV-E6
- MDM2
- HDM2
9
Q
diminishes p53 activity
A
HPV-E6
10
Q
promotes EMT
A
- FOXC2
- hypermethyllation of e-cadherin gene
- TWIST upregulation is associated with EMT
11
Q
Angiogenesis
A
- decreases with loss of HIF-1
- increased when there is a deleted or suppressed PKG
12
Q
telomere
A
- increases rebuilding potential: loss of TRF-1
- premature aging typically associated with telomere erosion
13
Q
rate of G1–> S transition
A
- increases rate: loss of P14-ARF
- reduces the latency: loss of Rh
14
Q
cell growth
A
- increase: active mTOR
- AKT (PKB) when over activated in cancer cells.