Growth, Cell death & Neoplasia Flashcards

1
Q

Define multiplicative growth

A

Increase in number of cells by mitotic cell divisions

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2
Q

Define auxetic growth

A

Increase in size of individual cells eg. Skeletal muscle

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3
Q

Define accretionary growth

A

Increase in intercellular tissue components

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4
Q

Define atrophy

A

Decrease in size of an organ or cell either physiological or pathological

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5
Q

Define hyperplasia

A

Increase in cell number by mitosis, may be due to decreased apoptosis

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6
Q

Define hypertrophy

A

Increase in cell size without cell division, in permanent cells it is the only option for growth

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7
Q

Define metaplasia

A

Reversible transformation of one fully differentiated cell type into another. It is an adaptive response to environmental stress. eg squamous epithelium –> columnar epithelium in Barrett’s oesophagus

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8
Q

3 characteristics of dysplasia

A

Increased cell growth, presence of atypical morphology, decreased differentiation, often pre-neoplastic, may be reversible in early stage

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9
Q

3 differences between apoptosis and necrosis

A

Apoptosis natural, necrosis caused by external factors. Apoptosis usually beneficial, necrosis always detrimental.
Apoptosis no symptoms, necrosis evokes an inflammatory response.

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10
Q

5 types of necrosis

A

Gangrenous, coagulative, colliquative, caseous, fat necrosis

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11
Q

Define neoplasia

A

Abnormal, uncoordinated and excessive cell growth which persists when the stimulus is removed

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12
Q

Define a tumour

A

A lesion resulting from the autonomous and abnormal growth of cells which persists after the initial stimulus has been removed

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13
Q

Name 6 different shapes of tumours

A

Sessile, pedunculated, fungating, papillary, ulcerated, annular

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14
Q

4 histological differences of neoplasms to normal tissue

A

Increased mitotic activity, loss of cellular cohesion, loss of differentiation, nuclear enlargement

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15
Q

8 inducers of apotosis

A

Growth factor withdrawal, loss of matrix attachment, glucocorticoids, viruses, free radicals, ionising radiation, DNA damage, FAS ligand

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16
Q

4 inhibitors of apoptosis

A

Growth factors, cell matrix, sex steroids, some proteins

17
Q

Describe the process of apoptosis

A

Degradation of cytoskeletal framework, DNA fragments, loss of mitochondrial function, nucleus shrinks (pyknosis) and fragments (karyorrhexis), cell shrinks but retains intact plasma membrane. Dead cells not phagocytosed break into apototic bodies - no inflammatory response.

18
Q

What two factors are tumours classified according to?

A

Behaviour (benign or malignant) and histogenesis (cell of origin)

19
Q

5 features of benign tumours

A

Close histological resemblance to parent tissue, non invasive, remain localised, slow growth, exophytic growth

20
Q

5 features of malignant tumours

A

Variable resemblance to parent tissue, ability to invade and therefore metastasise, rapid growing, endophytic growth

21
Q

5 clinical problems benign tumours can cause

A

Anxiety, pressure on surrounding structures, production of hormones, transformation into a malignant neoplasm, obstruction of the flow of fluid

22
Q

7 clinical problems malignant tumours cause

A

Pressure on/destruction of adjacent tissue, secondary tumours, anxiety, pain, paraneoplastic effects, blood loss, obstruction of flow, production of a hormone

23
Q

3 major histogenetic classifications

A

Epithelial, connective tissue, lymphoid/haemopoeitic organs

24
Q

Define differentiation

A

The degree to which the tumour resembles histologically its cell of origin, it determines the tumour grade

25
Q

What is a papilloma?

A

Benign tumour of non glandular/non secretory epithelium

26
Q

What is an adenoma?

A

Benign tumour of secretory/glandular epithelium

27
Q

What is a carcinoma?

A

Malignant tumour of non glandular epithelium

28
Q

What is an adenocarcinoma?

A

Malignant tumour of glandular epithelium

29
Q

What is a carcinoma in situ?

A

Epithelial neoplasm that has not yet invaded through the basement membrane. Only at this stage will excision guarantee a cure.

30
Q

How are benign mesenchymal tumour named?

A

After the cell/tissue of origin suffixed by ‘oma’ eg Lipoma - benign tumour of lipocytes

31
Q

What is a sarcoma?

A

Malignant tumour of mesenchyme/connective tissue. (prefixed by the cell/tissue of origin, eg. Osteosarcoma)

32
Q

What is a teratoma?

A

A neoplasm formed of cells representing all 3 germ layers - ectoderm, mesoderm and endoderm

33
Q

What are the two categories of tumour suppressor genes?

A

Caretaker genes (BRCA)- maintain integrity by repairing damaged DNA. Gatekeeper (p53) genes inhibit proliferation or promote death of cells with damaged DNA

34
Q

2 normal functions of p53

A

Repair of DNA by arresting the cell cycle in G1 until damage is repaired. Apoptotic cell death if damage is extensive

35
Q

Where is p53 situated?

A

Short arm of chromosome 17. (most frequently mutated)

36
Q

3 ways p53 can lose its normal function

A

Mutations (non sense or mis sense). Complexes of mutant and normal p53 inactivating the function of the normal allele. Binding of normal p53 protein to oncogenic DNA viruses.