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Cell Cycle and its implications
Dr. Lokendra Kunwar
MD Resident
Department of Clinical Oncology
Cell Cycle
• Sequence of events by which cell duplicates its genome and divides
into two identical daughter cells.
• Length of the Cell Cycle- depends on the type of cell that is dividing;
most of the cells in human body complete cell cycle in 24hrs.
Phases of Cell Cycle
• Interphase: Gap 1 (G1) phase – Gap 0 (G0)
Synthesis (S) phase
Gap 2 (G2) phase
• Mitosis phase:
Karyokinesis - Prophase, Metaphase, Anaphase, Telophase
Cytokinesis
Interphase
• Longest phase of the cell cycle.
• Preparation phase for redivison of a newly divided cell
• Series of changes take place in newly formed cell and its nucleus,
before it becomes capable of division again.
• 3 distinct phases
G1 phase
S phase
G2 phase.
Gap 1 (G1) phase
• First phase within the interphase
• Period of rapid growth
• Cell grows in preparation for DNA replication by synthesizing mRNA
and proteins, and certain intracellular components, such as
centrosomes undergo replication.
• Takes up about 1/3rd of the time of cell cycle.
• Determines whether a cell commits to divide or leaves the cell cycle.
• Ends after the cell move on to the S phase.
Synthesis (S) phase
• Follows G1 phase
• DNA replication occurs
• Strands of chromatin are copied, so that 2 new identical strands of
DNA are made; each chromosome now has 2 sister chromatids.
• Tightly regulated and widely conserved
Gap 2 (G2) phase
• Gap between DNA synthesis and mitosis.
• Period of rapid growth and cell prepares itself for mitosis.
• Proteins and enzymes related to cell division are synthesized.
• Stores energy which would be used during the division phase.
• G2 phase ends with the start of M phase.
G0 phase
• Resting phase where the cell has left the cell cycle and has stopped
dividing.
• Quiescent / Senescent state.
• Non proliferative cells generally enter this phase.
• Some cells remain quiescent for long periods of time like neurons.
• Some cells enter G0 phase semi permanently like hepatic and renal
cells.
Mitosis (M) phase
• Mitosis is the division of nucleus and cytoplasm of a parent cell into
two genetically identical daughter cells.
• Consists of Karyokinesis and Cytokinesis
Cell cycle phases
Cell Cycle Checkpoints
• Progression of cell cycle is highly regulated in certain points.
• These critical regulatory points of cell cycle are called Cell cycle
checkpoints.
• It ensures that:
- Genome is intact
- Conditions are appropriate for a cell to divide
- Genetic material is replicated completely in a cell cycle
- Chromosomes are correctly oriented in the metaphase plate
- All chromosomes are correctly attached to the spindle fibres.
3 checkpoints;
• G1 checkpoint (restriction checkpoint)
• G2 checkpoint (G2-M DNA damage checkpoint)
• Metaphase M checkpoint (Spindle assembly checkpoint)
G1 checkpoint
• Also called restriction point
• Operates at the end of G1 phase
• Checks whether:
- conditions are favorable for cell to undergo replication
• Checks DNA damage and directs the DNA repair mechanism to rectify
any DNA damage
• Mediated by cyclin E/CDK2 complex and Rb-E2F protein.
G2 checkpoint
• Operates at the end of G2 phase
• Checks for:
- Any damage to the DNA that might have occurred during DNA
replication
- Whether DNA is replicated completely
• Monitors the level of proteins and growth factors
• If any of the above factors are not satisfactory, G2 checkpoint holds
the cell at G2 phase and initate machineries to rectify the problems.
M checkpoint
• Operates at the end of metaphase.
• Checks for:
- Integrity of the spindle apparatus
- Correct orientation of chromosomes in metaphase plate
- Whether all chromosome are properly attached to the spindle fibres
• If chromosomes are not correctly attached to the spindle apparatus,
this checkpoint will stop the cell cycle.
Regulation of Cell Cycle
• Cyclins
• Cyclin Dependent Kinases (CDK)
• Cyclin Dependent Kinase Inhibitors (CDKI)
• Rb protein and E2F
Cyclins
• They are the family of proteins which regulates the cell cycle.
• Their concentration and expression cycles/varies during the cell cycle.
• Several types of cyclins are active during different phases of cell cycle
which bind to different types of CDKs and causes phosphorylation of
CDKs.
• Cyclins are synthesized and then actively degraded using ATP at
specific points in the cell cycle.
Cyclin Dependent Kinase
• CDKs are enzymes which activate the proteins required for
progression through the cell cycle and its checkpoints
• Inactive on their own but becomes active when attached to cyclin by
forming cyclin-CDK complex.
• Cyclin-CDK complexes then phosphorylates or attaches phosphate
group to certain domain on target proteins.
• The regulated activity of CDKs is essential for the transitions from G1
to S and from G2 to M.
Cyclin Dependent Kinase Inhibitors
• Inhibits CDKs
• Cell cycle is negatively controlled by CDKI
• Involved in cell cycle arrest at different phases of cell cycle.
Rb protein
• Initially identified as the product of the prototype tumor suppressor
gene, Rb.
• Prevents excessive cell division by regulating G1 checkpoint and
inhibiting cell cycle progression.
• Rb protein is normally bound to a transcription factor called E2F.
• Phosphorylation of Rb protein prevents its association with E2F,
thereby permitting E2F activation which causes transcription of genes
required for entry into S phase.
Cancer and cell cycle
• Cancer is a disease of abnormal proliferation and uncontrolled cell
division.
• Cell cycle misregulation and checkpoint genes mutation cause defect
in DNA synthesis and eventually cause cancer.
• Genes in which mutation gives rise to gain of function, leading to
malignancy are proto-oncogenes.
• Genes that give rise to loss of function mutations, leads to malignancy
are tumor suppressor genes.
• Proto-oncogenes- N ras, K ras, Her 2 neu, EGFR, ALK, N-myc, c-myc,
bcl2
• Tumor suppressor genes- Rb, p53, APC, BRCA, NF1, NF2, VHL
- Rb gene – Retinoblastoma, Osteosarcoma, Small cell lung cancer,
Breast cancer.
- p53 gene (Li Fraumeni Syndrome) - Sarcomas, Breast Ca, Leukemia,
Adrenal Ca.
Chemotherapy and cell cycle
• Rapidly growing neoplasia with a short cell cycle and larger
proportion of cells in S phase are highly responsive to chemotherapy.
• Many chemotherapeutic agents are cell cycle specific and produce
cytotoxic effect to tumor cells.
• Various drugs used in combination chemotherapy act at different
phases of cell cycle to produce maximum cell kill.
Radiotherapy and cell cycle
• G0, G1, S phase- Radioresistant.
• G2 and M phase- Radiosensitive.
THANK YOU

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CELL CYCLE.pptx

  • 1. Cell Cycle and its implications Dr. Lokendra Kunwar MD Resident Department of Clinical Oncology
  • 2. Cell Cycle • Sequence of events by which cell duplicates its genome and divides into two identical daughter cells. • Length of the Cell Cycle- depends on the type of cell that is dividing; most of the cells in human body complete cell cycle in 24hrs.
  • 3. Phases of Cell Cycle • Interphase: Gap 1 (G1) phase – Gap 0 (G0) Synthesis (S) phase Gap 2 (G2) phase • Mitosis phase: Karyokinesis - Prophase, Metaphase, Anaphase, Telophase Cytokinesis
  • 4.
  • 5. Interphase • Longest phase of the cell cycle. • Preparation phase for redivison of a newly divided cell • Series of changes take place in newly formed cell and its nucleus, before it becomes capable of division again. • 3 distinct phases G1 phase S phase G2 phase.
  • 6. Gap 1 (G1) phase • First phase within the interphase • Period of rapid growth • Cell grows in preparation for DNA replication by synthesizing mRNA and proteins, and certain intracellular components, such as centrosomes undergo replication. • Takes up about 1/3rd of the time of cell cycle. • Determines whether a cell commits to divide or leaves the cell cycle. • Ends after the cell move on to the S phase.
  • 7. Synthesis (S) phase • Follows G1 phase • DNA replication occurs • Strands of chromatin are copied, so that 2 new identical strands of DNA are made; each chromosome now has 2 sister chromatids. • Tightly regulated and widely conserved
  • 8. Gap 2 (G2) phase • Gap between DNA synthesis and mitosis. • Period of rapid growth and cell prepares itself for mitosis. • Proteins and enzymes related to cell division are synthesized. • Stores energy which would be used during the division phase. • G2 phase ends with the start of M phase.
  • 9.
  • 10. G0 phase • Resting phase where the cell has left the cell cycle and has stopped dividing. • Quiescent / Senescent state. • Non proliferative cells generally enter this phase. • Some cells remain quiescent for long periods of time like neurons. • Some cells enter G0 phase semi permanently like hepatic and renal cells.
  • 11. Mitosis (M) phase • Mitosis is the division of nucleus and cytoplasm of a parent cell into two genetically identical daughter cells. • Consists of Karyokinesis and Cytokinesis
  • 13. Cell Cycle Checkpoints • Progression of cell cycle is highly regulated in certain points. • These critical regulatory points of cell cycle are called Cell cycle checkpoints. • It ensures that: - Genome is intact - Conditions are appropriate for a cell to divide - Genetic material is replicated completely in a cell cycle - Chromosomes are correctly oriented in the metaphase plate - All chromosomes are correctly attached to the spindle fibres.
  • 14. 3 checkpoints; • G1 checkpoint (restriction checkpoint) • G2 checkpoint (G2-M DNA damage checkpoint) • Metaphase M checkpoint (Spindle assembly checkpoint)
  • 15. G1 checkpoint • Also called restriction point • Operates at the end of G1 phase • Checks whether: - conditions are favorable for cell to undergo replication • Checks DNA damage and directs the DNA repair mechanism to rectify any DNA damage • Mediated by cyclin E/CDK2 complex and Rb-E2F protein.
  • 16. G2 checkpoint • Operates at the end of G2 phase • Checks for: - Any damage to the DNA that might have occurred during DNA replication - Whether DNA is replicated completely • Monitors the level of proteins and growth factors • If any of the above factors are not satisfactory, G2 checkpoint holds the cell at G2 phase and initate machineries to rectify the problems.
  • 17. M checkpoint • Operates at the end of metaphase. • Checks for: - Integrity of the spindle apparatus - Correct orientation of chromosomes in metaphase plate - Whether all chromosome are properly attached to the spindle fibres • If chromosomes are not correctly attached to the spindle apparatus, this checkpoint will stop the cell cycle.
  • 18.
  • 19. Regulation of Cell Cycle • Cyclins • Cyclin Dependent Kinases (CDK) • Cyclin Dependent Kinase Inhibitors (CDKI) • Rb protein and E2F
  • 20. Cyclins • They are the family of proteins which regulates the cell cycle. • Their concentration and expression cycles/varies during the cell cycle. • Several types of cyclins are active during different phases of cell cycle which bind to different types of CDKs and causes phosphorylation of CDKs. • Cyclins are synthesized and then actively degraded using ATP at specific points in the cell cycle.
  • 21.
  • 22. Cyclin Dependent Kinase • CDKs are enzymes which activate the proteins required for progression through the cell cycle and its checkpoints • Inactive on their own but becomes active when attached to cyclin by forming cyclin-CDK complex. • Cyclin-CDK complexes then phosphorylates or attaches phosphate group to certain domain on target proteins. • The regulated activity of CDKs is essential for the transitions from G1 to S and from G2 to M.
  • 23.
  • 24. Cyclin Dependent Kinase Inhibitors • Inhibits CDKs • Cell cycle is negatively controlled by CDKI • Involved in cell cycle arrest at different phases of cell cycle.
  • 25. Rb protein • Initially identified as the product of the prototype tumor suppressor gene, Rb. • Prevents excessive cell division by regulating G1 checkpoint and inhibiting cell cycle progression. • Rb protein is normally bound to a transcription factor called E2F. • Phosphorylation of Rb protein prevents its association with E2F, thereby permitting E2F activation which causes transcription of genes required for entry into S phase.
  • 26.
  • 27. Cancer and cell cycle • Cancer is a disease of abnormal proliferation and uncontrolled cell division. • Cell cycle misregulation and checkpoint genes mutation cause defect in DNA synthesis and eventually cause cancer. • Genes in which mutation gives rise to gain of function, leading to malignancy are proto-oncogenes. • Genes that give rise to loss of function mutations, leads to malignancy are tumor suppressor genes.
  • 28. • Proto-oncogenes- N ras, K ras, Her 2 neu, EGFR, ALK, N-myc, c-myc, bcl2 • Tumor suppressor genes- Rb, p53, APC, BRCA, NF1, NF2, VHL - Rb gene – Retinoblastoma, Osteosarcoma, Small cell lung cancer, Breast cancer. - p53 gene (Li Fraumeni Syndrome) - Sarcomas, Breast Ca, Leukemia, Adrenal Ca.
  • 29. Chemotherapy and cell cycle • Rapidly growing neoplasia with a short cell cycle and larger proportion of cells in S phase are highly responsive to chemotherapy. • Many chemotherapeutic agents are cell cycle specific and produce cytotoxic effect to tumor cells. • Various drugs used in combination chemotherapy act at different phases of cell cycle to produce maximum cell kill.
  • 30.
  • 31. Radiotherapy and cell cycle • G0, G1, S phase- Radioresistant. • G2 and M phase- Radiosensitive.