W3- Lecture 16.2- Neoplasm 2 Flashcards

1
Q

Name the 4 histological changed of cancer progression

A
Normal 
Atypical 
Benign (non-cancerous)
Malignant 
Metastatic
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2
Q

Define dysplasia

A

Atypical cells (looks different )

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3
Q

Name the three cell cycle checkpoints where there is regulation of DNA damage

A

G1 checkpoint
G2 checkpoint
Mitotic spindle checkpoint

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4
Q
Review cell cycle 
G0
G1
S
G2
M
A

G0: RESTING phase where cell has left the cycle and stopped dividing.
G1: Cell increases in size-G1 Checkpoint ensures everything is ready for DNA synthesis.
S: DNA replication.
G2: Cell continues to grow- G2 checkpoint ensures everything is in place for mitosis
M: Cell growth stops at this stage and cellular energy is focused on the orderly division into two daughter cells.

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5
Q

What three genes help regulate

A

Oncogene
Tumour suppressor gene
DNA Repair gene

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6
Q

Describe the
Tumour suppressor gene
Oncogene
DNA repair gene

A

Tumour Suppressor Genes (-):
Loss of function of genes that inhibit cell cycle or that promote apoptosis.

Oncogenes (+):
Aberrant activation of genes that drive cell cycle, or that inhibit apoptosis.

DNA Repair Genes (-):
Loss of function of genes that protect cells from genetic damage, thus allowing accumulation of mutations that may affect TSGs or oncogenes.

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7
Q

Mutations disrupt the check marks leading to

A

Hyperplasia - dysplasia - in situ cancer - invasive cancer

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8
Q

What is an adenoma

A

benigntumourofepithelialtissue withglandularorigin, glandular characteristics, or both.

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9
Q

What is a carcinoma ?

A

type ofcancerthat develops fromepithelial cells.
begins in a tissue that lines the inner or outer surfaces of the body
And is malignant

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10
Q

Describe the evolution of a colorectal tumour (Adenomatous Polyposis Colon Cancer)

A

Mucosa (innermost wall) is attacked first

Formation of adenomas then carcinomas

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11
Q

What is the evolution of Adenomatous Polyposis Colon Cancer commonly driven by

A

loss of cell cycle inhibition and genomic stability

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12
Q

What is the Evolution Of A Uterine Tumour commonly driven by ?

A

Unopposed oestrogen signalling due to genetic alterations

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13
Q

What is a koilocyte?

A

A squamous epithelialcell that has undergone a number of structural changes, which occur as a result of infection of thecellbyhuman papillomavirus

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14
Q

What is the Evolution Of A Cervical Tumour commonly driven by ?

A

By viral infection e.g HPV

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15
Q

What is

Koilocytosisorkoilocytic atypiaorkoilocytotic atypia

A

(terms used inhistologyandcytologyto describe )

The presence of koilocytes in a specimen.

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16
Q

Name a cancer in which its progression is less clear then (colorectal, uterine and cervical ) and hence only detected at late stages as the early stages are unclear

A

Ovarian cancer

+ different types exist

17
Q

Is cancer homogeneous or heterogenous ?

A

heterogenous

18
Q

How care tumours defined ?

A
Tissue of origin.
Benign or malignant.
Tumour grade.
Tumour stage.
Tumour histology.
19
Q

Describe the term grade in terms of a tumour

A

appearance and behaviour when viewed under a microscope.

compared to normal cells

20
Q

Describe differentiation

+how is it described ?

A

how cancer cells look and function compared to normal cells

Described in degrees

21
Q

Describe what is meant by a cell being well-differentiated

A

cancer cells look and behave like the normal cells in the tissue they started to grow in.

22
Q

Describe what is meant by a cell being undifferentiated / poorly differentiated

A

cancer cells look and behave quite differently from normal cells in the tissue they started to grow in. They look immature or undeveloped and often do not resemble the tissue of origin at all.

23
Q

Describe benign tumours in terms of differentiation

A

Well-differentiated

Making it slower growing + less aggressive

24
Q

Describe the structure of benign and malignant cells

A

B-resemblance to normal cells (well differentiated )

M-abnormal less similarity to normal cells (anaplastic )

25
Q

Describe the mitoses of benign and malignant cells

A

B-few

M-relatively uncommon

26
Q

Describe the growth/ growth duration of benign and malignant cells

A

B-usually expansive
-may stop growing

M-invasive
-rarely stop growing

27
Q

Describe the encapsulation of benign and malignant cells

A

B-usually

M- rarely

28
Q

Describe the metastasis of benign and malignant cells

A

B- none

M-frequent

29
Q

Describe the effect on host of benign and malignant cells

A

B- slight hard due to location or complication

M-significant harm sure to invasion & metastasis

30
Q

What is the tumour grade based on ?

A

A measure of how abnormal the cancer cells look compared to normal tissue

  • appearance
  • mitotic behaviour
31
Q

What does a higher tumour grade mean ?

A

Higher the grade = the more abnormal the cells within the tumour look
+ the faster the growing it tends to be

32
Q

Why is cancer so hard to treat ?

A

It’s multifactorial and not all cancers have a set progression

33
Q

Define Gleason’s pattern for tumour grade

A

1 = small and uniform hence well differentiated
2/3= moderately differentiated
4/5= poorly differentiated
aka anaplastic

34
Q

What is tumour stage a measurement of ?

A

A measure of how far the tumour has disseminated + size

Also looking at lymph node involvement

35
Q

What are the four tumour stages

A

1=localised
2=Early localised but advancing
3=Late locally advanced
4=metastasised