Transcript Slide 1
Cell biology 2014 (12/2 -14)
Lecture 11:
A medical perspective
Definitions of disease:
•When something is wrong with a bodily function
• A state that places individuals at increased
risk of adverse consequences
• Etcetera
The cause of different diseases
Mendelian/Genetic
diseases
Heart disease
Allergy
100% genetics
100% environment
Diabetes
Cancer
Infectious
diseases
Complex multi-factorial diseases
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Three cytoskeleton systems:
distinct but overlapping functions
Intermediate filaments
Actin filaments
Microtubules
- Cell shape and integrity
- Motility of the whole cell or cellular appendages
- Intracellular organization
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Intermediate filaments and epithelia blistering
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Cytosolic intermediate filaments support:
1) Cell-cell contacts
(desmosomes: cadherins)
2) Cell-ECM contacts
(hemidesmosomes: integrins)
1 + 10
1.
5 + 14
2.
Albert et al Fig. 16-21
Mutations in keratin 5 or 14 cause Epidermolysis bullosa simplex
(1/40 000), a disease manifested as blistering of the epidermis.
Consequences of dysfunctional nuclear lamina
Lamin A, B & C: intermediate filament
proteins stabilize the nuclear envelope
Laminopathies are genetic diseases manifested as either:
I. Dystrophy of skeletal and/or heart muscles, caused by mutations
affecting Lamin A/B or proteins attaching lamins to the nuclear envelope
II. Progeria, caused by mutations in the lamin A gene, or
in a lamin A processing enzyme. This result in excessive
farnesylation. A farnesyltransferase inhibitor, initially
developed to target oncogenic Ras, delays progression.
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The actin cytoskeleton – an overview
• Support of the plasma membrane
• Cell migration
• Contraction
Muscle contraction
Cytokinesis
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Dysfunctional actin regulation in Wiskott-Aldrich syndrome
WASP
Arp 2/3
- Wiskott-Aldich syndrome (1/150.000) is caused by mutations
in the Wiskott-Aldrich syndrome protein (WASP)
WASP
Arp 2/3
ZZZZ
Manifested by:
• Thrombocytopenia
Underdeveloped cortical actin
results in defective platelets
• Eczema (skin blushing)
• Immunodeficiency syndrome
Deficient migratory and
phagocytotic capacity of
immune cells
- Can only be cured by a hematopoietic stem cell transplant
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Pathogenic E. coli: actin dependent colonization
Enteropathogenic E. coli induce actin
containing pedestals in intestinal epithelia
Virulence factors
that activate N-WASP
Activation of Arp 2/3
Loss of absorptive surface is one
cause for the associated diarrhea
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Listeria: actin dependent motility
1-3) Phagocytosis and escape
from phagosome
1.
2.
4) Bacterial multiplication
Arp 2/3
5) Penetration of a neighboring
cell through actin based motility
ActA
ActA
3.
ActA
4.
5.
video 24.3-listeria_parasites
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The microtubule system - an overview
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ER
- Intracellular
organization
Golgi
Organelle
positioning
Chromosome
segregation
Chemotactic agent
- Cell motility
Movement of
cellular appendages
Cell polarisation
and transport
Lissencephaly: defective neuron migration
- Lissencephaly ("smooth brain," 1/30.000) is a disorder
characterized by the lack of normal convolutions (folds) in the brain
Normal brain
Lissencephaly brain
mutated in many cases loss of dynein ( )
dependent centrosome reorientation defective cell polarization
Lis1
- 1/30 000 births, early death in severe cases
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Non-functional cilia in Kartagener syndrome
- Kartagener syndrome (1/20.000) is caused by mutations
affecting cilia specific dynein
- Manifested by respiratory infections, infertility and situs inversus
Upper respiratory epithelia
Patient with
Normal
Kartagener syndrome
Goblet
cell
Bacteria is caught in
mucus and cleared by
a cilia mediated flow
Bacteria is not cleared
due to defective cilia
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Microtubule-poisoning drug: Taxol
• Alkaloid ester isolated from the bark of
Taxus brevifolia (Pacific yew)
• Stabilization of microtubules
Therapeutic uses:
Treatment of breast, lung and ovarian cancer
Prevention of restenosis of coronary stents
(Surface coating of stents local action)
Major side-effects: Bone marrow suppression, gastro-intestinal
upset and peripheral neuropathy
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Microtubule-poisoning drug: Vinca alkaloids
• Isolated from Catharanthus roseus
• Named: Vinblastine, Vincristine, Vindesine
and Vinorelbine
• Sequesters tubulin
Therapeutic use:
Treatment of leukemia, lymphoma, breast,
lung, prostate, skin and testicular cancer
Major side-effects: Bone marrow suppression, gastro-intestinal
upset and peripheral neuropathy
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An oncology perspective on signal transduction, cell
growth, checkpoints, apoptosis and the cytoskeletons
Progression towards malignancy involves : i) uncontrolled proliferation,
ii) resistance to apoptosis, iii) cell migration, iv) tissue invasion
X X
X X
X X
X X
X X
Clonal evolution
Selection of
malignant clones
animation 20.2 -contact_inhibition
video 20.1 -breast_cancer_cells
X X
Metastasis
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Two distinct types of ”cancer genes”
Oncogenes
Gene X
Tumor suppressors
On
On
Off
Gene X
Off
Gene Y
Gene Y
On
Off
On
On
Gain-of-function
A single genetic change
Dominant phenotype
Loss-of-function
Two independent events
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Definitions: oncogenes and tumor suppressors
An oncogene is a gene that when mutated, or
overexpressed, contributes to converting a normal cell into
a tumor cell (constitutive activity dominant phenotype)
Ras
point mutation
Bcl-2
overexpression
A tumor suppressor-gene is a gene whose loss, or
inactivation, contributes to converting a normal cell into
a tumor cell (recessive phenotype)
CKI
p53
Rb
Inactivating point mutations or loss of the entire gene
(germ line mutation in one allele and/or acquired somatic mutations)
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Cell type specific proliferative signals
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Cells from different tissues express distinct sets of
growth factor receptors and signaling proteins
Cell type B
Cell type C
Cell type A
Major mitogen
signaling pathway: RTK
Alterations
in tumors:
RTK signals
Wnt
Hedgehog
Wnt signals
Hedgehog signals
Aberrant proliferative signals in tumors
Wnt
XGF
RTK
Ras
Hedgehog
Frizzled
Patched
Dishevelled
Smoothened
Raf
GSK-3b
Erk
b-catenin
myc
G1
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myc
Fused
Axin
SuFu
G1
Gli
Gli
myc
G1
Insensitivity of tumors to anti-growth signals
The retinoblastoma pathway
Mitogen signaling
p15
p21
= germ line
mutations identified
Cdk
G1
TGF-b
p16
HPV E7 viral
Rb
E2F
Cdk
P
Cdc6
P
ORC
S
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Evading cell death (apoptosis)
Survival factor signaling
BH3
only
p53
Ligand
Death
receptor
Adaptor
Bcl-2
Bax
Cyt. C
Caspase 9
Caspase 8
Caspase 3
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Apoptosis
Randomly acquired oncogenic mutations drives tumor progression
1 Self-sufficiency in proliferative signals
1.
Mutation
2 Insensitivity to anti-growth signals
2.
3.
3 Evading cell death (apoptosis)
4.
4 Limitless replicative potential
5 Sustained angiogenesis
5.
6 Metastasis capability
6.
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Same “diagnosis” but different set of mutations
4
3
4
5
6
X
3
X
2
X
1
X
Patient A with diagnosis X
2
5
6
X
X
1
X
Patient B with diagnosis X
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How many somatic mutations during a life time?
Cell death and
replacement
risk for mutations
& chromosomal
instability
Year 1-15
1013
Controlled and coordinated divisions
Uncontrolled divisions
Tumors
– Human diploid genome: ~6 x109 bp
– Only some few errors per replication cycle
– Average t½ of cells is 7 years (range: 24h to >100 years)
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Normal cells have a very low rate of mutations
Cancer related genes
Other genes
Random mutation
Time
Due to the low normal mutation frequency, progression
to a fully malignant tumor is statistically improbable
How come that malignant tumors have either a lot of
mutations (~10 %) or chromosomal aberrations (90 %)?
(~400 genes are frequently altered in tumors, 6 to 80 genes per “patient”)
Genomic instability: Two distinct levels
1. Defective DNA repair (MIN)
Mutation in a gene encoding some
enzyme required for DNA-repair
X
X
No repair many mutations
accelerated tumor progression
2. Chromosome segregation errors (CIN)
Mis-segregation due to a defective a gene that encodes some
protein essential for high fidelity chromosome segregation
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MIN reflects an escalated mutation rate
Cancer related genes
DNA repair (TS)
Other genes
Genetic alteration
Time
?? Often uncertain which ones of all the mutations that
contribute to tumor progression
1
2
3
4
5
6
MIN: mini-satellite DNA instability (due to defective DNA repair)
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CIN through excessive centrosomes
Two centromes
More than two centrosomes
Kinetochore attachments
satisfy the spindle checkpoint
CIN: Chromosomal instability
miss-segregation
aneuploidy
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CIN through loss of APC
The tumor suppressor gene product
APC functions as a MT plus-end
stabilizing protein (
) that facilitates
stable MT-kinetochore connections
Centromere
Centrosome
AC
APC
Kinetochore
CIN: Chromosomal instability
Satisfied
spindle
checkpoint
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CIN through a defective spindle checkpoint
1) A normal cell
Delayed anaphase until all
kinetochores are attached
2) A tumor cell with a (partially) defective spindle checkpoint
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Genomic instability and tumor progression
A stable genome
x
x
Too much
genetic
instability
”Optimal” genetic
instability
”Selection barriers”
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Principles of cancer treatment
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Surgery- Impossible to remove all cancer cells
Radiation-
Chemotherapy-
Targets both cancerand normal cells
Side-effects
General chemotherapy: drugs that interferes with:
i) DNA-replication
ii) DNA structure
iii) The function of the microtubule-system
Chemotherapy may also include cell type specific drugs.
E.g. inhibition of hormone dependent tumor growth
Selective killing of tumor cells by chemotherapy
x
x
Mutations that inactivate various checkpoints are common
in malignant tumors
no cell cycle arrest in patients treated by chemotherapy!
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