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CELL AND THE CELL CYCLE
BY DR. DEEPA GAUTAM
1st yr resident , Radiotherapy
• Cell is the basic structural, functional and
biological unit of all known living
organisms
• Often called as building blocks of life.
Cell organelles
• Cell membrane: protects inner cell and
regulates entry and exit of substances
• Mitochondria: power house of cell, site for
cellular respiration and ATP generation
• Ribosome: site for protein synthesis
• Endoplasmic reticulum:
– Rough: contains ER so site for protein
synthesis
– Smooth: lipid synthesis and drug
detoxification
• Golgi apparatus: packages proteins inside
the cell before send to destination.
• Lysosome: k/a suicidal bags, responsible
for cellular digestion by hydrolysis
• Microtubules : maintain the cellular
structure
• Microfilaments: cell motility
Nucleus
•Brain of cell
•Control all activities
within cell
•Contains genetic
material in the form
of nucleic acids
Nucleic acids
• Deoxyribonucleic acid(DNA)
• Ribonucleic acid (RNA)
Structure
• Nitrogen bases:
– Purines: Adenine, Guanine
– Pyrimidines: Thymine(DNA), Cytosine ,
Uracil(RNA)

• Pentose Sugar:
– Deoxyribose (DNA)
– Ribose(RNA)

• Phosphates
• Purines and pyrimidines are held together
by hydrogen bonds
• Sugar and phosphate linked together by
phosphodiester bonds
DNA

RNA

• Double stranded
• A=T, G= C
• Carries genetic
information in most of the
organisms

• Single stranded
• A=U, G=C
• Carries genetic
information in some
viruses
• Types:
– messenger RNA
– transfer RNA
– ribosomal RNA
Chromosome
•Organised structure
of DNA , protein and
RNA.
•Total 23 pairs of
chromosomes in
human beings with
21 somatic and 2
pairs of sex
chromosomes.
Gene
• The functional unit of inherited information
in DNA
• Represented by discrete section of
sequence that is necessary to encode a
particular protein structure
CELL CYCLE
PHASES OF CELL CYCLE
• G0 Phase
• Interphase (90% of cell cycle)
– Gap 1 (G1)
– Synthetic phase (S)
– Gap 2 (G2)

• Mitosis (10% of cell cycle)
G0
• Resting phase
• Cell leaves the cell cycle and stops
dividing
Interphase
•Preparation before
entering into cell
division
•Series of changes
take place in a
newly formed cell
and its nucleus
•Also k/a
preparatory phase
or inter mitosis
G1
• From end of previous M phase to
beginning of DNA synthesis
• Also k/a growth phase
• Biosynthesis of protein , enzymes required
for S phase needed for DNA replication
• Under control of p53 gene
S phase
• Starts when DNA replication starts
• Completes when all chromosomes have
been replicated and each chromosome
has sister chromatids
G2
• Gap between DNA synthesis and mitosis
• Cell grows
• Checked everything is ready to enter the
mitosis phase
Mitosis
• Divided into following phases:
– Prophase
– Prometaphase
– Metaphase
– Anaphase
– Telophase
Prophase
• Internal membranous compartments of
the cell including nucleus are
disassembled and dispersed
• Chromatids condense
• Protein synthesis ceases
prometaphase
• Bivalent attachment of chromosomes to
spindle dragging them to equator
Metaphase
• Proper equatorial alignment of
chromosomes on spindle
Anaphase
• Centromere divide
• Sister chromatids separate and lose
cohesion and pulled towards opposite
poles
Telophase
• Chromatids reach the opposite poles
• Nuclei and other membrane structures
reassemble
• Chromosomes recondense
• Karyokinesis is followed by cytokinesis
Regulation of cell cycle
• Regulation of entry and exit from
proliferation mode
• Co-ordination of cell cycle events
• Specialised responses that increase the
probability of environmental and internally
generated insults
Cyclin Dependent Kinase
• Proline directed serine threonine specific
protein kinase
• 2 subunits:
– Catalytic (CDK)
– Positive regulatory (Cyclin)
CDK function in cell cycle
Cell-Cycle Phase Transitions
• between G1 and S phase: cyclin A and E
dependent
• between G2 and M phase: Cyclin B and
CDK1 dependent
• within M phase that is between metaphase
and anaphase to preserve genomic
integrity
Checkpoints in cell cycle
• Damaged molecules make necessary
repairs
• Harmful cell cycle progression delayed
• DNA damage check points
• Replication check points
• Spindle integrity check points
DNA damage check points
• G1 and G2 checkpoints are p53
dependent while intra S phase DNA
damage checkpoint is not.
Replication checkpoints
• Functions like G2 DNA damage
checkpoint but through different pathway
• Mitotic entry blocked by inhibiting CDC25C
via action of chk1, preventing action of
CDK1
Spindle Integrity Checkpoint
• Mechanism of delay at prometaphase or
metaphase in response to spindle defects
or improper chromosome attachment
• Sensors of the defect are APC/C cofactor,
CDC20
• Cells are prevented from initiating
anaphase
Restriction point
• A point in mid G1
• Cells deprived of essential nutrients or
growth factor are blocked
Senescence
• Loss of capacity of proliferation
• Protective phenomenon against
malignancy
• Accumulation of high levels of CDK
inhibitors leading to permanent G1 arrest
• Lack of enzyme telomerase
Progressive shortening of telomere of
chromosome
Discontinuity of telomere
Chronic check point responses

Permanent cell cycle arrest
Cell Cycle and Cancer
• Cancer is a disease of uncontrolled
proliferation
Alterations in Pathways
• Growth and Proliferation Signaling
Pathways:
– Overexpression of receptors
– eg.Her-2/neu in ca breast
• Cell cycle machinery:
– Increased synthesis of cyclin D
– Increased degradation of CDK inhibitors
– Activation of CDK4/6
– Inactivation of tumour supression gene
• Senescence:
– mutations in gene encoding for DNA
checkpoints signaling elements most
commonly p53,
– Telomerase expression
Genetic and genomic instability
• Tumour supressor gene:
– mutation leading to loss of function gives rise
to cancer. Eg. p53, Rb , BRCA-1/2
– have recessive mutation i.e both alleles of
the chromosome need to be mutated

• Proto-oncogene:
– mutation leading to enhanced function gives
rise to cancer. Eg. RAS ,SRC kinase
– have dominant mutation i.e single allele
mutation.
• Stress Responses:
– Abnormal growth provokes stress response
leading to cell cycle arrest or cell death
– Eg. p53 required for DNA damage checkpoint
response as well as key effector of stress
response
– Mutation in p53 can lead to cancer by both
ways
Application of cell cycle in treatment
of cancer
• Radiotherapy
– Cells are most radiosensitive in mitotic phase
and least sensitive in S phase of cell cycle.
Chemotherapy and cell cycle
• G1 phase:
– L-Asparaginase

• S phase:
– Antimetabolites: 5-FU,
Capecitabine,Methotrexate,Gemcitabine
– Topoisomerase inhibitors:Etoposide,
Irinotecan
• G2 phase:
– Bleomycin (Anti-tumor antibiotics)

• M phase:
– Taxanes: Paclitaxel, Docetaxel
– Plant alkaloids: : Vincristine, vinblastine
• Cell cycle phase non-specific:
– Alkylating agents: Cyclophosphamide,
ifosphamide
– Anthracyclins: Doxorubicin, Epirubicin
– Platinum: Cisplatin, Carboplatin
– Antitumor antibiotics: Dactinomycin,
Mitomycin
Conclusion
• Cancer is a disease of alteration in cell
cycle and the knowledge of cell cycle can
be used in the treatment of cancer.

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Cell cycle

  • 1. CELL AND THE CELL CYCLE BY DR. DEEPA GAUTAM 1st yr resident , Radiotherapy
  • 2. • Cell is the basic structural, functional and biological unit of all known living organisms • Often called as building blocks of life.
  • 3.
  • 4. Cell organelles • Cell membrane: protects inner cell and regulates entry and exit of substances • Mitochondria: power house of cell, site for cellular respiration and ATP generation • Ribosome: site for protein synthesis • Endoplasmic reticulum: – Rough: contains ER so site for protein synthesis – Smooth: lipid synthesis and drug detoxification
  • 5. • Golgi apparatus: packages proteins inside the cell before send to destination. • Lysosome: k/a suicidal bags, responsible for cellular digestion by hydrolysis • Microtubules : maintain the cellular structure • Microfilaments: cell motility
  • 6. Nucleus •Brain of cell •Control all activities within cell •Contains genetic material in the form of nucleic acids
  • 7. Nucleic acids • Deoxyribonucleic acid(DNA) • Ribonucleic acid (RNA)
  • 8. Structure • Nitrogen bases: – Purines: Adenine, Guanine – Pyrimidines: Thymine(DNA), Cytosine , Uracil(RNA) • Pentose Sugar: – Deoxyribose (DNA) – Ribose(RNA) • Phosphates
  • 9. • Purines and pyrimidines are held together by hydrogen bonds • Sugar and phosphate linked together by phosphodiester bonds
  • 10.
  • 11. DNA RNA • Double stranded • A=T, G= C • Carries genetic information in most of the organisms • Single stranded • A=U, G=C • Carries genetic information in some viruses • Types: – messenger RNA – transfer RNA – ribosomal RNA
  • 12. Chromosome •Organised structure of DNA , protein and RNA. •Total 23 pairs of chromosomes in human beings with 21 somatic and 2 pairs of sex chromosomes.
  • 13. Gene • The functional unit of inherited information in DNA • Represented by discrete section of sequence that is necessary to encode a particular protein structure
  • 15. PHASES OF CELL CYCLE • G0 Phase • Interphase (90% of cell cycle) – Gap 1 (G1) – Synthetic phase (S) – Gap 2 (G2) • Mitosis (10% of cell cycle)
  • 16. G0 • Resting phase • Cell leaves the cell cycle and stops dividing
  • 17. Interphase •Preparation before entering into cell division •Series of changes take place in a newly formed cell and its nucleus •Also k/a preparatory phase or inter mitosis
  • 18. G1 • From end of previous M phase to beginning of DNA synthesis • Also k/a growth phase • Biosynthesis of protein , enzymes required for S phase needed for DNA replication • Under control of p53 gene
  • 19. S phase • Starts when DNA replication starts • Completes when all chromosomes have been replicated and each chromosome has sister chromatids
  • 20. G2 • Gap between DNA synthesis and mitosis • Cell grows • Checked everything is ready to enter the mitosis phase
  • 21. Mitosis • Divided into following phases: – Prophase – Prometaphase – Metaphase – Anaphase – Telophase
  • 22. Prophase • Internal membranous compartments of the cell including nucleus are disassembled and dispersed • Chromatids condense • Protein synthesis ceases
  • 23. prometaphase • Bivalent attachment of chromosomes to spindle dragging them to equator
  • 24. Metaphase • Proper equatorial alignment of chromosomes on spindle
  • 25. Anaphase • Centromere divide • Sister chromatids separate and lose cohesion and pulled towards opposite poles
  • 26. Telophase • Chromatids reach the opposite poles • Nuclei and other membrane structures reassemble • Chromosomes recondense • Karyokinesis is followed by cytokinesis
  • 27. Regulation of cell cycle • Regulation of entry and exit from proliferation mode • Co-ordination of cell cycle events • Specialised responses that increase the probability of environmental and internally generated insults
  • 28. Cyclin Dependent Kinase • Proline directed serine threonine specific protein kinase • 2 subunits: – Catalytic (CDK) – Positive regulatory (Cyclin)
  • 29. CDK function in cell cycle
  • 30. Cell-Cycle Phase Transitions • between G1 and S phase: cyclin A and E dependent • between G2 and M phase: Cyclin B and CDK1 dependent • within M phase that is between metaphase and anaphase to preserve genomic integrity
  • 31.
  • 32. Checkpoints in cell cycle • Damaged molecules make necessary repairs • Harmful cell cycle progression delayed
  • 33. • DNA damage check points • Replication check points • Spindle integrity check points
  • 34.
  • 35. DNA damage check points • G1 and G2 checkpoints are p53 dependent while intra S phase DNA damage checkpoint is not.
  • 36. Replication checkpoints • Functions like G2 DNA damage checkpoint but through different pathway • Mitotic entry blocked by inhibiting CDC25C via action of chk1, preventing action of CDK1
  • 37. Spindle Integrity Checkpoint • Mechanism of delay at prometaphase or metaphase in response to spindle defects or improper chromosome attachment • Sensors of the defect are APC/C cofactor, CDC20 • Cells are prevented from initiating anaphase
  • 38. Restriction point • A point in mid G1 • Cells deprived of essential nutrients or growth factor are blocked
  • 39. Senescence • Loss of capacity of proliferation • Protective phenomenon against malignancy • Accumulation of high levels of CDK inhibitors leading to permanent G1 arrest
  • 40. • Lack of enzyme telomerase Progressive shortening of telomere of chromosome Discontinuity of telomere Chronic check point responses Permanent cell cycle arrest
  • 41. Cell Cycle and Cancer • Cancer is a disease of uncontrolled proliferation
  • 42. Alterations in Pathways • Growth and Proliferation Signaling Pathways: – Overexpression of receptors – eg.Her-2/neu in ca breast
  • 43. • Cell cycle machinery: – Increased synthesis of cyclin D – Increased degradation of CDK inhibitors – Activation of CDK4/6 – Inactivation of tumour supression gene
  • 44. • Senescence: – mutations in gene encoding for DNA checkpoints signaling elements most commonly p53, – Telomerase expression
  • 45. Genetic and genomic instability • Tumour supressor gene: – mutation leading to loss of function gives rise to cancer. Eg. p53, Rb , BRCA-1/2 – have recessive mutation i.e both alleles of the chromosome need to be mutated • Proto-oncogene: – mutation leading to enhanced function gives rise to cancer. Eg. RAS ,SRC kinase – have dominant mutation i.e single allele mutation.
  • 46. • Stress Responses: – Abnormal growth provokes stress response leading to cell cycle arrest or cell death – Eg. p53 required for DNA damage checkpoint response as well as key effector of stress response – Mutation in p53 can lead to cancer by both ways
  • 47. Application of cell cycle in treatment of cancer • Radiotherapy – Cells are most radiosensitive in mitotic phase and least sensitive in S phase of cell cycle.
  • 48. Chemotherapy and cell cycle • G1 phase: – L-Asparaginase • S phase: – Antimetabolites: 5-FU, Capecitabine,Methotrexate,Gemcitabine – Topoisomerase inhibitors:Etoposide, Irinotecan
  • 49. • G2 phase: – Bleomycin (Anti-tumor antibiotics) • M phase: – Taxanes: Paclitaxel, Docetaxel – Plant alkaloids: : Vincristine, vinblastine
  • 50. • Cell cycle phase non-specific: – Alkylating agents: Cyclophosphamide, ifosphamide – Anthracyclins: Doxorubicin, Epirubicin – Platinum: Cisplatin, Carboplatin – Antitumor antibiotics: Dactinomycin, Mitomycin
  • 51. Conclusion • Cancer is a disease of alteration in cell cycle and the knowledge of cell cycle can be used in the treatment of cancer.