pt 6 Flashcards

(50 cards)

1
Q

What does ‘cellular adaptation’ mean in the context of pathology?

A

Cellular adaptation refers to the ways cells adjust their structure and function in response to increased or decreased demands or stress, often to avoid injury or keep functioning.

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2
Q

Under what circumstances does a cell typically undergo hypertrophy vs. hyperplasia?

A

Hypertrophy: When cells increase in size, due to synthesis of more structural components (often seen in tissues with limited cell division, e.g., muscle). Hyperplasia: When cells increase in number via cell division (e.g., epithelial or glandular tissues).

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3
Q

Define hyperplasia, and how does it differ from cancerous growth?

A

Hyperplasia: A controlled increase in the number of cells, leading to tissue/organ enlargement. Cancerous growth: An uncontrolled proliferation that does not respond to normal regulatory signals.

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4
Q

What are the main molecular mechanisms that can trigger hyperplasia?

A
  1. Increased local production of growth factors. 2. Increased expression of growth factor receptors on cells. 3. Enhanced intracellular signalling pathways that lead to gene transcription and cell proliferation.
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5
Q

What is hypertrophy, and what are common examples of physiological vs. pathological hypertrophy?

A

Hypertrophy: Increase in cell size (and thus organ size) due to increased synthesis of structural proteins. Physiological example: Skeletal muscle hypertrophy from exercise. Pathological example: Cardiac hypertrophy in response to hypertension or valve disease.

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6
Q

Summarize the two main biochemical pathways leading to muscle hypertrophy.

A
  1. Physiological: IGF-1 → PI3K → Akt pathway (e.g., muscle growth from exercise). 2. Pathological: Ang II, ET-1, or NA → G-protein-coupled receptors (Gαq/11) → MAPK/PKC/PKA → excessive or maladaptive hypertrophy (e.g., heart under high blood pressure).
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7
Q

Differentiate hyperplasia from hypertrophy with a simple example.

A

Hyperplasia: Four cells → eight cells (cell number doubles, same size). Hypertrophy: Four cells → four enlarged cells (cell size increases, number unchanged).

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8
Q

What is atrophy, and why can it be considered an adaptive process?

A

Atrophy is the shrinkage (reduced size) of a tissue or organ due to decreased cell size and number. It’s adaptive because it helps cells/tissues minimize energy demands or resources if stimuli (e.g., blood flow, nutrition) are reduced.

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9
Q

List some common causes of atrophy.

A
  1. Decreased workload (disuse) 2. Loss of innervation (denervation) 3. Diminished blood supply (ischemia) 4. Inadequate nutrition 5. Loss of endocrine stimulation 6. Pressure (compression)
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10
Q

What is metaplasia, and when might it occur?

A

Metaplasia is when one mature cell type changes to another mature cell type better able to endure new conditions (e.g., respiratory epithelium changing to squamous in a smoker’s airways).

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11
Q

Define ‘healing responses’ after injury and how regeneration differs from scar formation.

A

Healing is the body’s way of restoring tissue integrity post-injury. Regeneration fully replaces damaged cells with original cell types, preserving function. Scar formation (fibrosis) uses collagen and fibrous tissue to patch damage, potentially losing normal function.

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12
Q

What factors determine whether healing occurs primarily by regeneration or by fibrosis (scar formation)?

A
  1. Tissue’s intrinsic ability to regenerate (e.g., labile vs. stable vs. permanent cells). 2. Extent of the injury (smaller or superficial injuries more likely to regenerate; extensive damage often leads to scarring).
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13
Q

Give examples of tissues that exhibit continuous (labile), stable, and permanent cell turnover.

A

Labile (continuous): Skin epidermis, GI tract epithelium, hematopoietic cells. Stable: Liver, kidney tubule cells (can regenerate if needed). Permanent: Neurons, cardiac muscle (minimal to no regenerative capacity).

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14
Q

Why is stem cell function crucial for tissue regeneration?

A

Stem cells can self-renew and differentiate into needed mature cells, making them vital for replacing lost or damaged cells in regenerative tissues (e.g., skin, gut lining, bone marrow).

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15
Q

Compare embryonic stem cells (ES) with adult (somatic) stem cells.

A

ES cells: Pluripotent, can form all tissue types; found in the inner cell mass of blastocysts. Adult stem cells: Typically multipotent or more lineage-restricted, reside in specific niches (e.g., bone marrow, basal layer of skin).

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16
Q

What are induced pluripotent stem cells (iPSCs), and why might they overcome some ethical or rejection issues?

A

iPSCs are adult somatic cells (e.g., skin fibroblasts) genetically reprogrammed to pluripotent status. Because they originate from the patient’s own cells, they sidestep many immune rejection and ethical problems associated with embryonic stem cells.

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17
Q

What is the main safety concern in using stem cells for regenerative therapy?

A

Their intrinsic capacity for rapid proliferation and self-renewal can, if dysregulated, lead to tumorigenesis (i.e., formation of teratomas or other malignancies).

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18
Q

Why is understanding stem cell biology important for advancing medical research and therapy?

A
  1. Elucidates developmental signals and differentiation steps. 2. Aids in creating knockout models for disease study. 3. Enables potential regeneration of damaged organs (e.g., cell-based transplant therapies).
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19
Q

What is ‘growth’ in the context of tissue biology?

A

Growth is the process by which a tissue increases in size through the synthesis of specific cellular components.

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20
Q

How is ‘differentiation’ defined?

A

Differentiation is the process by which a cell develops a specialized function or morphology that distinguishes it from its parent cells.

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21
Q

What does ‘tumour differentiation’ refer to?

A

It refers to the extent to which neoplastic cells resemble the normal cells of the tissue from which they arise, both morphologically and functionally.

22
Q

Define ‘anaplasia.’

A

Anaplasia is the loss of cellular differentiation—a reversion from a highly differentiated state to a less specialized, primitive state—and is a hallmark of malignant transformation.

23
Q

Name one morphological change seen in anaplastic cells.

A

Pleomorphism, which is marked variation in cell size and shape.

24
Q

Give another example of a change associated with anaplasia.

A

Abnormally large nuclei that contain an abundance of DNA relative to the cell size.

25
What is 'neoplasia'?
Neoplasia is the process of new, uncontrolled cell growth that forms a neoplasm or tumour, which grows uncoordinated with normal tissues.
26
How is a tumour defined?
A tumour is an abnormal mass of tissue resulting from neoplasia, where the growth exceeds and is uncoordinated with that of the normal tissue, persisting even after the original stimulus ceases.
27
What distinguishes a benign tumour from a malignant tumour?
Benign tumours are non-invasive, remain localized, have a slow growth rate, and are often encapsulated, whereas malignant tumours are invasive, can metastasize, grow rapidly, and exhibit disordered cellular architecture.
28
How are benign epithelial tumours commonly named?
They are typically called papillomas or adenomas.
29
How are malignant epithelial tumours named?
Malignant epithelial tumours are called carcinomas.
30
What term is used for malignant connective tissue tumours?
They are known as sarcomas.
31
What does the suffix '-oma' indicate in tumour nomenclature?
It is used to denote a neoplasm or tumour, whether benign or malignant, though additional descriptors clarify behavior (e.g., carcinoma, sarcoma).
32
Define metaplasia.
Metaplasia is a reversible change in which one differentiated adult cell type is replaced by another that is better able to withstand adverse conditions.
33
Why is metaplasia clinically important?
Although adaptive, persistent metaplasia may predispose tissue to dysplasia and subsequent malignant transformation.
34
What is dysplasia?
Dysplasia is disordered growth where cells lose uniformity and proper orientation; it is often a pre-neoplastic lesion seen especially in metaplastic epithelia.
35
List one characteristic of dysplastic cells.
They exhibit considerable pleomorphism with variable cell shapes and sizes.
36
What is a hyperchromatic nucleus?
A nucleus that stains more darkly due to an increased DNA content, often seen in dysplastic or malignant cells.
37
What does 'metastasis' mean?
Metastasis is the process by which tumour cells spread from the primary site to distant locations, forming secondary tumour implants.
38
Name one common route of metastatic spread.
Lymphatic spread, where tumour cells travel through lymphatic vessels to regional lymph nodes.
39
What is another pathway for metastasis?
Haematogenous spread, in which tumour cells enter the bloodstream and form metastases in distant organs.
40
What does 'direct seeding' refer to in metastasis?
Direct seeding is the spread of tumour cells across body cavities or surfaces (e.g., pleural, pericardial, or peritoneal cavities).
41
What are oncogenes?
Oncogenes are mutated forms of normal growth-promoting genes that drive uncontrolled cell proliferation.
42
What is the function of tumour suppressor genes?
Tumour suppressor genes normally inhibit cell proliferation; their inactivation removes these growth restraints, contributing to carcinogenesis.
43
What role do apoptosis-regulating genes play in cancer?
They control programmed cell death, and when altered, they can allow damaged cells to survive and proliferate.
44
What are DNA repair genes?
DNA repair genes are responsible for correcting genetic errors; defects in these genes lead to accumulation of mutations that can drive carcinogenesis.
45
Define hyperplasia.
Hyperplasia is an increase in the number of cells within a tissue, resulting in tissue enlargement.
46
What is hypertrophy?
Hypertrophy is the increase in the size of individual cells, leading to an increase in tissue mass.
47
What does atrophy refer to?
Atrophy is the reduction in cell size or number, resulting in the shrinkage of a tissue.
48
How do benign tumours differ from malignant tumours regarding local invasion?
Benign tumours are non-invasive and remain localized, while malignant tumours invade surrounding tissues and can metastasize.
49
What is the significance of a fibrous capsule in benign tumours?
A fibrous capsule helps separate benign tumours from the surrounding tissue, making them well-circumscribed and often easier to remove surgically.
50
Which of the following is not used in cancer therapy: surgical removal, radiotherapy, chemotherapy, growth hormone therapy, or immunotherapy?
Growth hormone therapy is not used as a treatment for cancer.