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Chapter 8 - Part1
Chapter 8 - Part1
• Cancer cells
• start out as normal body cells,
• undergo genetic mutations,
• lose the ability to control the tempo of their own division, and
• cause disease.
• Cancer therapy seeks to disrupt one or more steps in cell division.
• Cell division
• is reproduction at the cellular level,
• produces two “daughter” cells that are genetically identical to each
other and the original “parent” cell,
• requires the duplication of chromosomes, the structures that contain
most of the cell’s DNA, and
• sorts new sets of chromosomes into the resulting pair of daughter cells.
1. Prokaryotes have short strands of circular 1. Eukaryotes have long strands linear double-stranded
double-stranded DNA DNA molecules.
3. The single chromosome is present in the nucleoid. 3. Several chromosomes are present inside the nucleus.
4. Present in the cytoplasm of the cell 4. Present in the nucleus of the cell.
5. The chromosomes lacks centromeres and telomeres. 5. It contains several centromeres and telomeres.
6. It encodes for only few proteins. 6. It encodes for large number of proteins.
8.1 Cell division plays many important roles in the lives of
organisms
Division into
3
two daughter cells
• Eukaryotic cells
• are more complex and larger than prokaryotic cells,
• have more genes, and
• store most of their genes on multiple chromosomes within the nucleus.
• Each eukaryotic species has a characteristic number of
chromosomes in each cell nucleus.
Sister chromatids
Chromosome
duplication
Sister
chromatids
Centromere
Separation
of sister
chromatids
and
distribution
into two
daughter
cells
© 2016 Pearson Education, Ltd.
8.3 The large, complex chromosomes of
eukaryotes duplicate with each cell division
Chromosome
duplication
Sister
chromatids
Centromere
Separation
of sister
chromatids
and
distribution
into two
daughter
cells
© 2016 Pearson Education, Ltd.
8.4 The cell cycle includes growing and division phases
• Cell cycle is the period between one cell division and the next.
G1 S
(first gap) (DNA synthesis)
M
k inesis is G2
t o s
Cy ito (second gap)
M
• A mitotic spindle
• is required to divide the chromosomes,
• guides the separation of the two sets of daughter chromosomes, and
• is composed of microtubules and associated proteins.
• Spindle microtubules emerge from two centrosomes,
microtubule-organizing regions in the cytoplasm of eukaryotic cells.
Nuclear Centromere
Plasma Spindle
envelope membrane Chromosome, consisting
microtubules
of two sister chromatids
• Interphase
• The cytoplasmic contents double.
• Two centrosomes form.
• Chromosomes duplicate in the nucleus during the S phase.
MITOSIS
INTERPHASE Prometaphase
Prophase
Centrosomes Fragments of
Chromatin Early mitotic Centrosome the nuclear envelope
spindle
Kinetochore
• Prophase
• In the nucleus, chromosomes become more tightly coiled and folded.
• In the cytoplasm, the mitotic spindle begins to form as microtubules
rapidly grow out from the centrosomes.
• Prometaphase
• The nuclear envelope breaks into fragments and disappears.
• Microtubules extend from the centrosomes into the nuclear region.
• Some spindle microtubules attach to the kinetochores.
• Other microtubules meet those from the opposite poles.
MITOSIS
Metaphase Anaphase Telophase and Cytokinesis
Metaphase plate
Cleavage
furrow
Nuclear
envelope
Separated
Mitotic spindle forming
chromosomes
• Metaphase
• The mitotic spindle is fully formed.
• Chromosomes align at the cell equator.
• Kinetochores of sister chromatids are facing the opposite poles of the
spindle.
• Anaphase
• Sister chromatids separate at the centromeres.
• Daughter chromosomes are moved to opposite poles of the cell as
motor proteins move the chromosomes along the spindle microtubules
and kinetochore microtubules shorten.
• Spindle microtubules not attached to chromosomes lengthen, moving
the poles farther apart.
• At the end of anaphase, the two ends of the cell have equal collections
of chromosomes.
• Telophase
• The cell continues to elongate.
• The nuclear envelope forms around chromosomes at each pole,
establishing daughter nuclei.
• Chromatin uncoils.
• The mitotic spindle disappears.
Cytokinesis
Cleavage furrow
Contracting ring of
microfilaments
Daughter cells
Cytokinesis New
cell wall
Daughter
nucleus
Cell plate
forming Cell plate
Vesicles containing Daughter cells
cell wall material
Anchorage
dependence: cells
anchor to the dish
surface and divide
Density- dependent
inhibition: When cells
have formed a
complete layer, they
stop dividing.
Removal of cells
Note:
1. Cancer cells
are not subject
to anchorage Restoration of single
dependence;
layer by cell division
they grow
whether or not
they are in 2. density-
contact to Cancer cells forming dependent
suitable clump of overlapping inhibition fails
surface cells in tumor.
© 2016 Pearson Education, Ltd.
When grown in the lab, cells fail to
divide if an essential nutrients is left
out of the culture medium.
Growth Factor: is a protein
molecule made by the body; it
Cultured cells
functions to regulate cell division &
cell survival.
suspended in liquid
For example, a protein called
vascular endothelial growth factor The addition of
(VEGF) stimulates the growth of
growth
new blood vessels during fetal
development and after injury.
factor
G0
G1
S
Control
system
G2
M checkpoint
G2 checkpoint
© 2016 Pearson Education, Ltd.
A checkpoint is a stage in the eukaryotic cell cycle at which
the cell examines internal and external cues and "decides"
whether or not to move forward with division.
• Cancer currently claims the lives of 20% of the people in the United
States.
• Cancer cells escape controls on the cell cycle.
• Cancer cells divide excessively and invade other tissues of the body.
Lymph
vessels
Blood
vessel
Tumor
Tumor in
another
Glandular part of
tissue the body