Tumour Pathology 5 Flashcards

(31 cards)

1
Q

What influences disorders of cell growth?

A
  • Tumour suppressor genes
  • Inherited factors in carcinogenesis
  • Oncogenes
  • Viral carcinogenesis
  • Precursors of cancer
  • Multistep process of tumour development
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2
Q

What influences carcinogenesis?

A
  • Geographic and environmental factors
  • Age
  • Hereditary
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3
Q

What are proto-oncogenes?

A

-Normal genes that promote normal cell growth and mitosis

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4
Q

What are tumour suppressor genes?

A

Normal growth inhibiting genes

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5
Q

What do tumour suppressor genes include?

A
  • Genes negatively regulating mitosis-Rb
  • Genes regulating apoptosis
  • Genes regulating DNA repair
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6
Q

What usually happen to tumour suppressor genes before a normal cell transforms into a cancer cell?

A

A series of several mutations

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7
Q

What is a key event in tumour formation?

A

Uncontrolled cell proliferation via cell cycle dysregulation via loss of tumour suppressor gene function

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8
Q

What is the retinoblastoma gene?

A

An anti-oncogene

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9
Q

What do Rb gene mutations favour?

A

Cell proliferation

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10
Q

What mimics the effect of pRb loss?

A

Mutations in other genes controlling pRb phosphorylation

  • Mutational activation of cyclin D or CDK4
  • Mutational inactivation of CDKIs also drive proliferation
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11
Q

What releases the cell cycle brake?

A

Absent or inactive pRb

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12
Q

What has to happen to tumour suppressor genes for cancer to arise?

A

There must be loss/inactivation of both normal allelic copies

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13
Q

Describe the 2 hit hypothesis in the inherited and sporadic forms of anti-oncogenes such as Rb.

A
Inherited form
-One defective inherited copy of pRb
-Somatic point mutation of other copy
Sporadic form
-Both hits occur in a single cell
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14
Q

What chromosome contains the defective inherited copy of pRb?

A

13q14

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15
Q

How can carcinogenesis be hereditary?

A
  • Inherited cancer syndromes
  • Familial cancers
  • Autosomal recessive syndromes of defective DNA repair
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16
Q

Describe inheritance of cancer syndromes?

A
  • Strong family history of uncommon site-specific cancers

- Autosomal dominant inheritance of a single mutant gene

17
Q

Give examples of inherited cancer syndromes?

A
  • Familial retinoblastoma
  • Familial adenomatous polyposis of colon
  • Multiple endocrine neoplasia
  • Neurofibromatosis
  • Von Hippel-Lindau syndrome
18
Q

Describe familial cancers.

A
  • Family clustering of cancers but individual predisposition unclear
  • Multifactorial inheritance
  • Early age of onset
  • Multiple/bilateral tumours
19
Q

Give examples of familial cancers.

A
  • Some breast cancers
  • Some ovarian cancers
  • Non-FAP colon cancers
20
Q

What are oncogenes?

A

Cancer causing genes derived from proto-oncogenes

21
Q

How are oncogenes activated?

A

Alteration of proto-oncogene structure
-Point mutation
-Chromosome rearrangements and translocations
Dysregulation of proto-oncogene expression
-Gene amplification
-Overexpression

22
Q

What do oncogenes generate?

A

Active oncoprotein products

23
Q

Give examples of active oncoprotein products.

A
  • Growth factors
  • Growth factor receptors
  • Proteins involved in signal transduction
  • Nuclear regulatory proteins
  • Cell cycle regulators
24
Q

What are 2 exampled of cancer which can arise as a result of overexpression of oncogenes?

A
  • Burkitt lymphoma: C-myc moves close to IgH gene

- Mantle cell lymphoma: cyclin D1 gene to IgH

25
Give an example of a cancer that results due to recombination to form chimeric proteins.
Chronic myeloid leukaemia
26
What DNA viruses are known to cause cancer in humans?
- HPV (cervical cancer) - Hepatitis B (liver cancer) - EBV (Burkitt lymphoma)
27
What are the different mechanisms or viral carcinogenesis?
- Virus genome inserts near a host proto-oncogene - Viral promoter or other transcription regulation elements cause proto-oncogene over-expression - Retroviruses insert an oncogene into host DNA causing cell division
28
What is a DNA adduct?
A chemical carcinogen or their active metabolite which reacts to form covalently bound products
29
How does chemical carcinogenesis work?
DNA adduct formation at particular chromosome sites lead to activation of oncogenes and suppression of anti-oncogenes
30
Why is carcinogenesis considered a multistep process?
- All sporadic cancers harbour multiple genetic aberrations - Abnormalities accumulate with time - Activation of several oncogenes and loss of 2 or more anti-oncogenes occurs in most cancers
31
What are the key regulators in cancer?
- p16 - cyclin D - CDK4 - Rb - In the majority of cancers these are mutated