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Why does cell proceed towards
carcinogenesis when there are
mechanisms to remove cells unfit for
survival?
Why does cell proceed towards
carcinogenesis when there are
mechanisms to remove cells unfit for
survival?
Monika
Roll no: M-5626
Division of veterinary medicine
Monika
Roll no: M-5626
Division of veterinary medicine
Robinns basic pathology
• Process of actual formation of cancer which is
characterised by progression of changes at the
- Genetic
- Epigenetic level
- Ultimately lead to uncontrolled cell division
• Multistep process
Robinns basic pathology
Carcinogenesis?Carcinogenesis?
Hanahan et
al.,2011
Robinns pathology
MECHANISMS TO REMOVE CELL UNFIT
FOR SURVIVAL
MECHANISMS TO REMOVE CELL UNFIT
FOR SURVIVAL
ApoptosisApoptosis
• Apoptosis is a active energy dependent process that involves
cleavage of DNA by endonucleases and proteins by proteases
called CASPASES.
Lowe et al., 2000
Robinns pathology
Necrosis
• Local death of tissue within living tissue after degradative
action of enzymes on the irreversible injured cell
• Potentially reversible process in which a cell that is stressed EATS
itself.
Elmore., 2007
• Characterized by the formation of cytoplasmic AUTOPHAGIC
VESICLES
• Targeted disruption of genes such as ATG5 that are involved in
autophagy can inhibit cell death.
• Autophagy has dual roles in cancer:
- a tumor suppressor by preventing the accumulation of damaged
proteins and organelles
- as a mechanism of cell survival that can promote the growth of
tumors
Tait et al., 2014
Factors leading to defective autophagy:
a)Beclin 1 mutation
b) PI3K-Akt-mTOR pathway dysregulation
Panda et al.,
2015
What makes the cell to evade cell
death and makes it cancerous?
What makes the cell to evade cell
death and makes it cancerous?
Hanahan et al., 2011
Robinns pathology
Over expression of telomeraseOver expression of telomerase
Checkpoints in cell cycle
the cell cycle is controlled by two classes of cell cycle
proteins,
cyclins and cyclin dependent kinases (CDKs),
which physically associate to form a protein
kinase that drives the cell cycle forward
the cell cycle is controlled by two classes of cell cycle
proteins,
cyclins and cyclin dependent kinases (CDKs),
which physically associate to form a protein
kinase that drives the cell cycle forward
most tumor cells lack the
DNA damage-induced p53-
dependent G1 checkpoint,
increasing the likelihood
that mutations will be
propagated in these cells.
most tumor cells lack the
DNA damage-induced p53-
dependent G1 checkpoint,
increasing the likelihood
that mutations will be
propagated in these cells.
Molecular Biology of Cancer
• Situated at the short arm of 17 chromosome
• Mutated in most of the cancer cases
• Repair of damaged DNA before S-phase in the cycle by
arresting cell cycle in G1 phase untill the damage is repaired
• Apoptic cell death if there is extensive DNA damage
• p53 can lost its function:
a) Non sense mutation or mis sense mutation
b) Binding of normal p53 to viral oncoproteins
p53p53
Molecular Biology of Cancer
Mutated p53Mutated p53
Fas/FADD downregulationFas/FADD downregulation
High levels of FLICE
FADD like IL-1 converting enzymeFADD like IL-1 converting enzyme
Binds with DISC(death inducing signalling complex)Binds with DISC(death inducing signalling complex)
Prevents activation of caspases 8Prevents activation of caspases 8
No
apoptosis
No
apoptosis
Elmore.,2007
Over expression of Bcl-2Over expression of Bcl-2
• Caretaker genes
- Maintain the integrity of the genome by repairing DNA
damage
• Gatekeeper genes
- Inhibit the proliferation or promote the death of cells with
damaged DNA
Categories of tumor suppressor genesCategories of tumor suppressor genes
28
Rb geneRb gene
RAS gene
• APC regulates the rates of proliferation and apoptosis
• APC is important for cytoskeletal integrity, cellular adhesion,
and Wnt signaling.
• APC plays a role in the G1/S transition of the cell cycle by
modulating expression levels of c-myc and cyclin D1
• full length APC is also important in maintaining intestinal cell
migration up the crypt and inducing apoptosis
APC(Adenomatous polyposis coli)APC(Adenomatous polyposis coli)
Martinez et al.,2003
tumor suppressor gene ,role in induction of cell cycle
arrest and apoptosis
tumor suppressor gene ,role in induction of cell cycle
arrest and apoptosis
acts as a negative regulator of Akt activationacts as a negative regulator of Akt activation
can induce apoptosis of mutated Or stressed cells to
prevent tumor formation
can induce apoptosis of mutated Or stressed cells to
prevent tumor formation
PTEN suppresses the PI-3K-mediated induction of blood
vessel growth factors
PTEN suppresses the PI-3K-mediated induction of blood
vessel growth factors
PTENPTEN
Martinez et
Other factors..
family of Inhibition of Apoptosis Proteins
- xIAP,BIRC2,BIRC3
Heat Shock Proteins
- HSP27,HSP70
Casarett & Doull’s Toxicology 7th
edition
• deregulation in anoikis execution is emerging as a hallmark of
cancer cells and contributes to the formation of metastasis in
distant organs
Paoli et al., 2013
Conclusion
 Oncogenic mutation distrupt apoptosis ,leading to tumor
initiation,progression and metastasis
 Agents that induce apoptosis,autophagy can be used as
anticancer drugs
 p53 mutation causes Li- Fraumenic syndrome
 Bcl-2 alteration causes hodgkin disease,breast cancer
 Bax deletion causes brain tumors
Role of apoptosis in cancer progression

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Role of apoptosis in cancer progression

  • 1. Why does cell proceed towards carcinogenesis when there are mechanisms to remove cells unfit for survival? Why does cell proceed towards carcinogenesis when there are mechanisms to remove cells unfit for survival? Monika Roll no: M-5626 Division of veterinary medicine Monika Roll no: M-5626 Division of veterinary medicine
  • 3. • Process of actual formation of cancer which is characterised by progression of changes at the - Genetic - Epigenetic level - Ultimately lead to uncontrolled cell division • Multistep process Robinns basic pathology Carcinogenesis?Carcinogenesis?
  • 4.
  • 7. MECHANISMS TO REMOVE CELL UNFIT FOR SURVIVAL MECHANISMS TO REMOVE CELL UNFIT FOR SURVIVAL
  • 8.
  • 9.
  • 10. ApoptosisApoptosis • Apoptosis is a active energy dependent process that involves cleavage of DNA by endonucleases and proteins by proteases called CASPASES. Lowe et al., 2000
  • 12. Necrosis • Local death of tissue within living tissue after degradative action of enzymes on the irreversible injured cell
  • 13. • Potentially reversible process in which a cell that is stressed EATS itself. Elmore., 2007 • Characterized by the formation of cytoplasmic AUTOPHAGIC VESICLES • Targeted disruption of genes such as ATG5 that are involved in autophagy can inhibit cell death. • Autophagy has dual roles in cancer: - a tumor suppressor by preventing the accumulation of damaged proteins and organelles - as a mechanism of cell survival that can promote the growth of tumors Tait et al., 2014
  • 14. Factors leading to defective autophagy: a)Beclin 1 mutation b) PI3K-Akt-mTOR pathway dysregulation Panda et al., 2015
  • 15. What makes the cell to evade cell death and makes it cancerous? What makes the cell to evade cell death and makes it cancerous? Hanahan et al., 2011
  • 16.
  • 18. Over expression of telomeraseOver expression of telomerase
  • 19. Checkpoints in cell cycle the cell cycle is controlled by two classes of cell cycle proteins, cyclins and cyclin dependent kinases (CDKs), which physically associate to form a protein kinase that drives the cell cycle forward the cell cycle is controlled by two classes of cell cycle proteins, cyclins and cyclin dependent kinases (CDKs), which physically associate to form a protein kinase that drives the cell cycle forward most tumor cells lack the DNA damage-induced p53- dependent G1 checkpoint, increasing the likelihood that mutations will be propagated in these cells. most tumor cells lack the DNA damage-induced p53- dependent G1 checkpoint, increasing the likelihood that mutations will be propagated in these cells. Molecular Biology of Cancer
  • 20.
  • 21. • Situated at the short arm of 17 chromosome • Mutated in most of the cancer cases • Repair of damaged DNA before S-phase in the cycle by arresting cell cycle in G1 phase untill the damage is repaired • Apoptic cell death if there is extensive DNA damage • p53 can lost its function: a) Non sense mutation or mis sense mutation b) Binding of normal p53 to viral oncoproteins p53p53 Molecular Biology of Cancer
  • 24. High levels of FLICE FADD like IL-1 converting enzymeFADD like IL-1 converting enzyme Binds with DISC(death inducing signalling complex)Binds with DISC(death inducing signalling complex) Prevents activation of caspases 8Prevents activation of caspases 8 No apoptosis No apoptosis Elmore.,2007
  • 25. Over expression of Bcl-2Over expression of Bcl-2
  • 26.
  • 27. • Caretaker genes - Maintain the integrity of the genome by repairing DNA damage • Gatekeeper genes - Inhibit the proliferation or promote the death of cells with damaged DNA Categories of tumor suppressor genesCategories of tumor suppressor genes
  • 30. • APC regulates the rates of proliferation and apoptosis • APC is important for cytoskeletal integrity, cellular adhesion, and Wnt signaling. • APC plays a role in the G1/S transition of the cell cycle by modulating expression levels of c-myc and cyclin D1 • full length APC is also important in maintaining intestinal cell migration up the crypt and inducing apoptosis APC(Adenomatous polyposis coli)APC(Adenomatous polyposis coli) Martinez et al.,2003
  • 31.
  • 32. tumor suppressor gene ,role in induction of cell cycle arrest and apoptosis tumor suppressor gene ,role in induction of cell cycle arrest and apoptosis acts as a negative regulator of Akt activationacts as a negative regulator of Akt activation can induce apoptosis of mutated Or stressed cells to prevent tumor formation can induce apoptosis of mutated Or stressed cells to prevent tumor formation PTEN suppresses the PI-3K-mediated induction of blood vessel growth factors PTEN suppresses the PI-3K-mediated induction of blood vessel growth factors PTENPTEN Martinez et
  • 33. Other factors.. family of Inhibition of Apoptosis Proteins - xIAP,BIRC2,BIRC3 Heat Shock Proteins - HSP27,HSP70 Casarett & Doull’s Toxicology 7th edition • deregulation in anoikis execution is emerging as a hallmark of cancer cells and contributes to the formation of metastasis in distant organs Paoli et al., 2013
  • 34. Conclusion  Oncogenic mutation distrupt apoptosis ,leading to tumor initiation,progression and metastasis  Agents that induce apoptosis,autophagy can be used as anticancer drugs  p53 mutation causes Li- Fraumenic syndrome  Bcl-2 alteration causes hodgkin disease,breast cancer  Bax deletion causes brain tumors