MCB Lecture 64 Neoplasia I Flashcards

0
Q

Describe pathological and physiologic causes of hyperplasia

A

Pathological: too many growth factors, hormones
Physiological: growth of the uterus during pregnancy

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1
Q

Describe pathological and physiologic causes of hypertrophy

A

Pathological: hypertension, leading to increased heart cell size and stenosis
Physiological: athletes heart, lifting weights: increased muscle size

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2
Q

Describe two causes of metaplasia

A

Smoking: ciliated columnar epithelium replaced with stratified squamous
Barrett oesophagus: simple squamous replaced with columnar in response to gastric acid reflux

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3
Q

What is dysplasia?

A

Pre malignant condition of proliferation

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4
Q

What are the features of cells that have undergone dysplasia?

A

Loss of cell polarity
Loss of tissue architecture
Atypical mitoses
Proliferation

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5
Q

What is the outcome of dysplasia?

A

Expected progression on to cancer

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6
Q

What is neoplasia?

A

New growth of cells

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7
Q

What is the name for the study of cancer?

A

Oncology

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8
Q

What suffix is used to denote benign neoplasms?

A

-oma

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9
Q

What are the features of benign neoplasms?

A

Well differentiated
Discrete location
Can not invade and replace healthy tissues
Can’t metastasise

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10
Q

What is cystic teratoma?

A

This is an example of a benign neoplasm

It arises from stem cells, so many different tissue types are see that produce hair, teeth and secrete stuff

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11
Q

What are the features of malignant neoplasms?

A

They can metastasise and invade and replace healthy tissues
They are no longer well differentiated
They are not localised to a discrete area
Much dysplasia
Less differentiated

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12
Q

What are the most common cancers?

A

The gender specific cancers such as breast and prostate are the most common

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13
Q

Which cancers contribute to the most deaths?

A

Lung, colorectal, breast and prostate

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14
Q

What is an individual’s lifetime risk of cancer?

A

1/3

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15
Q

What are the two broad categories of aetiology of cancer?

A

Environmental and hereditary

16
Q

What are some environmental causes of cancer?

What are the common features of the mode of action of these things?

A

Smoking, industrial, dietary

They all contain highly reactive oxygen species that make the genome unstable

17
Q

All cancer, hereditary or otherwise, is due to …

A

Genomic instability

18
Q

Why are double stranded breaks dangerous?

A

When the cell tries to repair this, mistakes are often made, leading to mutations

19
Q

What does non-ionising radiation do?

A

Makes thiamine dimers

20
Q

What does ionising radiation do?

A

Causes double and single stranded breaks

21
Q

Describe how oncogenic viruses cause cancer

eg?

A

They insert genes into the host genome. This may disrupt tumour suppressor genes

HPV, EDV

22
Q

Describe how immunodeficiency leads to cancer

Eg. ?

A

When an individual is immunosupressed, they can not kill neoplastic cells and many tumours result

E. HIV

23
Q

How can chronic inflammation lead to cancer?

A

The cytokines and other inflammatory substances are highly reactive

24
Q

How can genetics play a role in cancer?

A

Gene mutation of an oncogene or tumour suppressor gene

Eg. BRCA-1, Rb gene, APC

25
Q

What are the 5 methods of detection of cancer?

A
Physical examination
Histology / cytology
Tumour markers
Imaging 
Molecular diagnosis
26
Q

Describe how physical examination is used to detect cancer

A

This is no longer sufficient

27
Q

Describe how cytology and histology is used to detect cancer

A

Looking at biopsies under the microscope: cell numbers and tissue structure etc.

28
Q

Describe how tumour markers are used to detect cancer

What are the two main ways this is done?

A

Immunohistochemistry: using MHC that is specific for antigens involved with cancer
Eg. EGF receptor is the antigen. MHC binds, and is seen because it is marked

Biochemical assay: same thing, done in the blood

29
Q

Describe how imaging is used to detect cancer

A

Inject isotopically marked glucose and then use PET scanning to see where is highly metabolically active

30
Q

How can cancers be diagnosed molecularly:

  • What are we looking for?
  • How can we find it?
A

PCR: eg. Of BCR-abl to detect residual leukaemia cells in CML

Genome wide profiling: microarrays, RNA-seq

31
Q

Describe the difference in survival rate when breast cancer is detected early

A

Early detection: 98% survival over next 5 years

32
Q

What are the two modes of staging of cancer?

Which is the most useful?

A

Grading
Staging

Staging is more useful

33
Q

Describe how grading of cancer is done

A

Look at the cells and grade them based on:
Level of differentiation
Mitoses
Architecture

Give it a grade from low to high

34
Q

Describe how staging of cancer is done

A

Stage it based on: size of primary lesion T
Presence of metastasis M
Extent of spread to region lymph nodes N

35
Q

Describe the TNM system of cancer staging

A

T: size of primary tumour
M: presence of metastasis
N: extent of spread to the regional lymph nodes

Eg T1-T4