Lecture 6 Flashcards

(73 cards)

1
Q

Neoplasm meaning

A

Neo=new, plasm= growth. New AND abnormal growth of tissue

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2
Q

Neoplasm is interchangeable with the word ….

A

Cancer. But we use neoplasm instead of cancer as it has a very negative connotation. (Neoplasm is used to talk about cancer by health professionals so patients don’t hear them).

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3
Q

In the modern world, is cancer more treatable and managable?

A

Yes, as there are more treatments being created

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4
Q

Oncology meaning

A

The study and treatment of tumours. (The study of cancer S most tumours are cancerous)

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5
Q

Metastasise meaning

A

Secondary malignant growths (on tumour) at a distance from primary site. Metastasised tumour is a tumour that is spreading from primary tumour out to different tissues and systems of the body.

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6
Q

What is the most dangerous types of tumours?

A

Metastasised tumours as it is very difficult to track down these metastasis or metastic events throughout the body and throughout the bodily systems as there are a variety of mechanisms by which they can travel through the body.

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7
Q

Cancer meaning

A

A disease caused by an uncontrolled division/ growth of abdominal cells in a part of the body (neoplasm)

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8
Q

What are the GENERAL (popular but not seen in every type of these cells) features of a neoplastic cell(cell going through cancerous change)?

A

SOCAAA.
S: loss of specialised function; abnormality of growth leads to loss of their specialised function, if neoplasticism cells maintain their function then they’re technically not neoplasticism cells, may just be metaplasia (change in type of cell-can develop extra functions but never looses function) or even dysplasia (less likely). In order for cell to be classed as neoplastic, it will have to be abnormal and have lost its specialised function in that regard.
O: uses less oxygen; able to divide and grow with less oxygen input from the blood vessels, which helps them to develop into areas with less/weak blood supply- key features of malignant tumours, mostly in areas of less blood flow but can thrive there as they require less oxygen to create damage.
C: loss of contact inhibition; contact inhibition is when cells that are in contact with other cells of the same origin or type, they are inhibited in their growth. Cells clustered together all bunched together in a small space, these cells are telling each other through this physiological process that there’s no need to grow, or divide unnecessarily because this area of the body is full of those cells. When you take one off these cells out of the tissue and put it into just simply the extra cellular matrix and its not in contact with other cells, then that cell is being told by the extra cellular environment that there’s no other cells around, and you should probably start dividing because that tissue of the body might need to regenerate, or repair or just fill out the space that is essentially empty around that cell.When there’s no room cells don’t divide as often, when there’s more room, cells will divide more often to fill that space. Tissues hate having holes in them, they hate having empty spaces, they r often quickly filled w either normal healthy tissue or scar tissue. (Clusters of cells near each other inhibiting each other from growing and dividing because the space is full, neoplastic cells lose this contact inhibition- leading to excessive growth of cells/neoplastic cells)
A: better adapted to anaerobic conditions; goes through an anaerobic biochemical processes at a much faster rate, than healthy cells,
A:autonomous growth; growth in the absence of any external stimulus (abscesses of; growth hormones, sex hormones, increased blood supply to an area) required to stimulate neoplastic cells to grow, they do IIT automatically without any hormonal or humoural stimulation to force them to grow)
A: anaplasia; loss of growth. Ana= lack, plasma= growth. A condition where we have less differentiation of these cells, they lose their morphological characteristics, similar to dysplasia (lack of differentiation and normal features of cells that give them their specialised function).

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9
Q

Neoplastic cell feature - loss of specialised function explanation

A

Abnormality of growth leads to loss of their specialised function, if neoplastic cells maintain their function then they’re technically not neoplastic cells, may just be metaplasia (change in type of cell-can develop extra functions but never looses function) or even dysplasia (less likely). In order for cell to be classed as neoplastic, it will have to be abnormal and have lost its specialised function in that regard. - goes with anaplasia feature.

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10
Q

Neoplastic cell feature- uses less oxygen

A

Able to divide and grow with less oxygen input from the blood vessels, which helps them to develop into areas with less/weak blood supply- key features of malignant tumours, mostly in areas of less blood flow but can thrive there as they require less oxygen to create damage.

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11
Q

Neoplastic cell feature- loss of contact inhibition

A

Contact inhibition is when cells that are in contact with other cells of the same origin or type are inhibited in their growth. Cells clustered together all bunched together in a small space, these cells are telling each other through this physiological process that there’s no need to grow, or divide unnecessarily because this area of the body is full of those cells. When you take one off these cells out of the tissue and put it into just simply the extra cellular matrix and its not in contact with other cells, then that cell is being told by the extracellular environment that there’s no other cells around, and you should probably start dividing because that tissue of the body might need to regenerate, or repair or just fill out the space that is essentially empty around that cell.When there’s no room cells don’t divide as often, when there’s more room, cells will divide more often to fill that space. Tissues hate having holes in them, they hate having empty spaces, they r often quickly filled w either normal healthy tissue or scar tissue. (Clusters of cells near each other inhibiting each other from growing and dividing because the space is full, neoplastic cells lose this contact inhibition- leading to excessive growth of cells/neoplastic cells)

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12
Q

Neoplastic cell feature - better adapted to anaerobic conditions

A

A: better adapted to anaerobic conditions; goes through an anaerobic biochemical processes at a much faster rate, than healthy cells.

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13
Q

Neoplastic cell feature - autonomous growth

A

Growth in the absence of any external stimulus (abscesses of; growth hormones, sex hormones, increased blood supply to an area) required to stimulate neoplastic cells to grow, they do IIT automatically without any hormonal or humoural stimulation to force them to grow)

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14
Q

Neoplasticism cell feature - anaplasia

A

A: anaplasia; loss of growth. Ana= lack, plasma= growth. A condition where we have less differentiation of these cells, they lose their morphological characteristics, similar to dysplasia (lack of differentiation and normal features of cells that give them their specialised function

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15
Q

How can cancers and tumours be classified?

A

In a number of ways. Classified/named according to their tissue origin, also by how they behave, behavioural classification is very simple, its binary. Behavioural classification is either benign or malignant.

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16
Q

Benign tumour meaning

A

“Good” type of cancer or less severe type of tumour that we’ll see clinically.

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17
Q

Malignant tumour meaning

A

More aggressive, more dangerous and clinically relevant form of tumour that leads to all of the downstream sequelae, that is familiar w cancers.

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18
Q

Features of benign tumours

A

VMEDS
V: often poor vascularity- double edged sword. Poor vascularity means that tumour is typically slower growing than it would be if it had a higher level of vascularity, but poor vascularity can sometimes lead to the centre of the lesion/tumour becoming necrotic, because if it is so far away from blood supply n cut off from blood supply by the encapsulation, its very hard for the nutrients and oxygen to diffuse into the centre of that tumour and then it can become necrotic and cause its own issue(inflammatory changes and negative side effects as well).
M: no metastases- they do not spread, doesn’t break off and spread to different parts of the body or different areas of the same tissue. They are a centralised tumour, a lump/clump/growth that is all centralised in one place and is not spreading.
E: usually encapsulated; they have a capsule around them(made of a thin sheet of connective tissue-areolar, or dense irregular connective tissue), if not encapsulated there is a very clear distinction between where the tumour starts and ends, so where the tumour is and where the normal healthy tissue is surrounding that tumour. Clear distinction between benign tumour cells and healthy cells around them.
D: usually greater differentiation than malignant - has more differentiation, still resembles normal healthy cells (parenchymal cells) that surround them.
S: usually slow growing- can vary depending on situation our enviornment in which they exist.

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19
Q

Features of benign tumour: poor vascularity

A

V: often poor vascularity- double edged sword. Poor vascularity means that tumour is typically slower growing than it would be if it had a higher level of vascularity, but poor vascularity can sometimes lead to the centre of the lesion/tumour becoming necrotic, because if it is so far away from blood supply n cut off from blood supply by the encapsulation, its very hard for the nutrients and oxygen to diffuse into the centre of that tumour and then it can become necrotic and cause its own issue(inflammatory changes and negative side effects as well).

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20
Q

Features of benign tumour - no metastes

A

M: no metastases- they do not spread, doesn’t break off and spread to different parts of the body or different areas of the same tissue. They are a centralised tumour, a lump/clump/growth that is all centralised in one place and is not spreading.

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21
Q

Features of benign tumours- usually encapsulated

A

E: usually encapsulated; they have a capsule around them(made of a thin sheet of connective tissue-areolar, or dense irregular connective tissue), if not encapsulated there is a very clear distinction between where the tumour starts and ends, so where the tumour is and where the normal healthy tissue is surrounding that tumour. Clear distinction between benign tumour cells and healthy cells around them.

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22
Q

Features of benign tumours - usually greater differentiation than malignant

A

D: usually greater differentiation than malignant - has more differentiation, still resembles normal healthy cells (parenchymal cells) that surround them.

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23
Q

Features of benign tumours - usually slow growing

A

can vary depending on situation our enviornment in which they exist.

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24
Q

Features of malignant tumours

A

Mud Roi
M; metastasise
U;less uniformity;l not as easy to seperate visually from the tissue around them because of the infiltration and movement and the spreading they aren’t as uniform and even the internal contents aren’t as uniform. Many different things happening in these malignant cells at the same time which leads to less uniformity.
D; less differentiation- further away from the apparent chymal or Normal cells that surround them, look messy and looses physical characteristics that provided their particular function long ago.
R: can spread rapidly; if they form metastic sub local cells
O; often vascular- most of them can produce the proteins that essentially trigger angiogenesis and formation of new blood vessels, into that area into the body, can sometimes redirect blood flow from normal parenchymal healthy tissue around them and into the tumour itself to feed that tumour and increase the growth rate and the expansion of that tumour as well.
I: infiltrate; infiltrates other tissues, organs, organ systems or the space around that primary tumour outwards like a vine.
Features that lead to most clinical classification is: infiltrate and metastasise.

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25
Features malignant tumours - less uniformity
U;less uniformity;not as easy to seperate visually from the tissue around them because of the infiltration and movement and the spreading they aren’t as uniform and even the internal contents aren’t as uniform. Many different things happening in these malignant cells at the same time which leads to less uniformity.
26
Features of malignant tumours - less differentiation
D; less differentiation- further away from the apparent chymal or Normal cells that surround them, look messy and looses physical characteristics that provided their particular function long ago.
27
Malignant tumours features - spreads rapidly
R: can spread rapidly; if they form metastic sub local cells
28
Features of malignant tumour - often vascular
O; often vascular- most of them can produce the proteins that essentially trigger angiogenesis and formation of new blood vessels, into that area into the body, can sometimes redirect blood flow from normal parenchymal healthy tissue around them and into the tumour itself to feed that tumour and increase the growth rate and the expansion of that tumour as well.
29
Features of malignant tumour - infiltration
I: infiltrate; infiltrates other tissues, organs, organ systems or the space around that primary tumour outwards like a vine.
30
What are the histological classifications of tumours?
- Relates to tissue of origin. - -oma can be associated with malignant or beinign tumours (neoplasticity). - 2 types: sarcoma and carcinoma
31
What is sarcoma?
Cancer that begins in bone, cartilage, fat, muscle, blood vessels, or other connective or supportive tissue in the body. Origin = connective tissue.
32
What is carcinoma?
Cancer that originates in the skin or in the tissues that line or cover internal; organs (epithelia). A majority (close to 90%) of cancer are carcinoma- very common, as epithelial cells are constantly being replenished by stem cells and going through the cell cycle - More vulnerable to carcinogenic and genetic changes that lead to cancer. Origin = epithelia cells (squamous, cuboidal, columnar epithelia).
33
What is carcinoma?
Cancer that originates in the skin or in the tissues that line or cover internal; organs (epithelia). A majority (close to 90%) of cancer are carcinoma- very common, as epithelial cells are constantly being replenished by stem cells and going through the cell cycle - More vulnerable to carcinogenic and genetic changes that lead to cancer. Origin = epithelia cells (squamous, cuboidal, columnar epithelia).
34
What is a benign tumour in adipose tissue termed as?
Lipoma
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What is a benign tumour in adult fibrous tissue termed as?
Fibroma
36
What is a malignant tumour in adipose tissue called?
Liposarcoma
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What is a malignant tumour in adult fibrous tissue termed as?
Fibrosacrcoma
38
What is mesothelioma?
Malignant tumour in the mesothelioma, referring to cancer in the lung.
39
What is a Teratoma?
A tumour. Has 3 diffferent types of tissue- each of which come from a different germ layer in the body (mesoderm, endoderm, ectoderm) within the tumour. Eg. GIT lining, epidermis and cartilage in histological image (abnormal). Can have developed teeth or hair in it like swallowing twin (this type is mostly benign). But more normal looking teratomas are malignant. Usually unnoticed - no symptoms unless malignant Mostly found in gonads(testes, ovaries).
40
What is a Teratoma?
A tumour. Has 3 diffferent types of tissue- each of which come from a different germ layer in the body (mesoderm, endoderm, ectoderm) within the tumour. Eg. GIT lining, epidermis and cartilage in histological image (abnormal). Can have developed teeth or hair in it like swallowing twin (this type is mostly benign). But more normal looking teratomas are malignant. Usually unnoticed - no symptoms unless malignant Mostly found in gonads(testes, ovaries).
41
Most types of tumours and cancer come from…
A single origin, a single adult mature tissue origin
42
How do cancerous cells develop?
Via the multistep theory of carcinogenesis (origin of carcinoma). Steps include: initiation, promotion, progression and latency (IPPL).
43
multi-step theory of carcinogenesis - initiation explanation
The initiation step in the multi-step theory of carcinogenesis is when a normal cell undergoes changes that give it the potential to become cancerous (neoplastic). This transformation happens when a single cell is altered, but it's a complex process that usually requires more than one factor to trigger it.
44
How does the initiation process in carcinogenesis typically happen?
The initiation can involve several things: - Multiple genetic changes or mutations. - Exposure to environmental factors like chemicals or hormones. - A combination of genetic changes and environmental exposures happening at the same time.
45
Can the initiation of neoplastic change happen spontaneously?
Yes, initiation can be spontaneous due to normal cell division and genetic changes that occur as cells replicate.
46
Why is cancer more common in older individuals?
Older individuals have cells that have gone through more cycles of division, increasing the chance of genetic mutations or errors that can lead to cancer.
47
How does the frequency of cell division relate to cancer risk?
the more a cell divides, the greater the chance for genetic mutations to occur, which increases the risk of neoplastic changes.
48
Why is cancer less common in younger individuals?
Younger individuals have cells that have divided fewer times, so the likelihood of genetic changes or mutations occurring is lower.
49
What role do carcinogens play in the initiation of cancer?
Carcinogens can cause genetic changes in cells, but they often require long-term exposure or a combination with other factors to initiate cancer.
50
How does the body detect and respond to mutations in cells?
The body’s defense system, such as the p53 protein, can detect genetic changes and trigger apoptosis (cell death) to eliminate potentially cancerous cells.
51
Why might the body not be able to eliminate cancerous cells exposed to carcinogens?
Prolonged exposure to carcinogens (such as from bacterial infections) can overwhelm the body’s defense systems, allowing the mutations to persist and the cells to avoid apoptosis.
52
Is the initiation of cancer a simple "on/off" process?
No, initiation is a complex and multifactorial process involving a combination of genetic changes, environmental factors, and the body's response to these changes.
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multi-step theory of carcinogenesis - promotion explanation
The promotion step of this multi-step theory is essentially the clonal proliferation of transformed (neoplastic) cell, where the cell divides and produces more neoplastic daughter cells.
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What happens during the promotion step of carcinogenesis?
After a cell becomes neoplastic, it divides, and its daughter cells also become neoplastic. This process repeats, increasing the number and size of neoplastic cells.
56
Can a neoplastic cell divide properly during the promotion step?
A neoplastic cell can undergo changes and become potentially cancerous, but if it cannot divide properly, the daughter cells may die due to genetic instability.
57
What happens if a neoplastic cell has a drastic genetic change?
If the genetic change in the neoplastic cell is severe, it may lead to instability in the genetic material of daughter cells, causing them to die after division.
58
What is the purpose of the promotion step in carcinogenesis?
The promotion step verifies that the neoplastic change (initiated earlier) can be passed on to subsequent generations of cells, ensuring the neoplastic transformation continues in the daughter cell population.
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How does promotion affect the size of the neoplastic cell population?
Promotion increases the size of the neoplastic cell population by promoting the division and growth of neoplastic cells and their daughter cells.
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Is the promotion step about verifying the stability of neoplastic cells?
Yes, promotion helps confirm that the neoplastic change can be propagated to future generations of cells, ensuring continued growth and expansion of the cancerous cell population.
61
multi-step theory of carcinogenesis - progression explanation
Progression is the process that results in malignant behavior, where cancer cells invade surrounding tissues, leading to clinical consequences.
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What characterises the progression of a neoplastic cell?
The progression is marked by the invasion of different tissues and the resulting harmful effects, such as loss of function or pressure on surrounding normal tissues.
63
How can tissue invasion during progression affect the body?
Invasion can reduce the function of critical parenchymal tissues or create pressure on surrounding tissues, leading to clinical symptoms.
64
What happens when cancer cells invade areas with important parenchymal functions?
The invasion of these areas leads to a reduction in their function, which can cause clinical effects, like organ dysfunction.
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How does the progression step affect the tumor's behavior?
Progression leads to the expansion of the tumor and its transformation into a malignant state, where it becomes more aggressive and invasive.
66
What does the term "progression" refer to in terms of malignancy?
Progression refers to the tumor’s movement into a more malignant stage, where it becomes capable of invading surrounding tissues and causing more severe damage.
67
multi-step theory of carcinogenesis - latency explanation
The latency period is the time between the exposure to a carcinogen or initiation of the neoplastic change and the actual development of the tumor.
68
What happens during the latency period?
During latency, a small cluster of neoplastic cells gradually grows into a larger cluster.
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What is the clinical relevance of the latency period?
the latency period is when clinical effects start to appear as the tumor grows and invades surrounding tissues, leading to symptoms like tissue damage, lack of blood flow, or functional impairment.
70
How can tumor growth during the latency period affect surrounding tissues?
The growing tumor can invade nearby tissues, causing them to die due to lack of blood flow, or disrupt normal function, such as invading vital structures like the pericardium or the brain.
71
What kinds of clinical effects might emerge during the latency period?
Clinical effects include tissue death (due to reduced blood flow), loss of function in organs or structures (like the pericardium or brain), or compression of surrounding tissues, leading to neurological disruptions.
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Why is the latency period important in cancer progression?
The latency period marks the time when the tumor grows undetected until it reaches a size or location where it starts to cause symptoms or clinically detectable changes in the body.
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