Tumour Pathology 2 Flashcards

1
Q

Properties of cancer cells: What are examples of loss of tumour suppressor genes?

A
  • Adenomatour Polyposis
  • Retinoblastoma
  • BRCA1
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Properties of cancer cells: What are examples of gain of function of oncogenes?

A
  • B-raf
  • Cyclin D1
  • Erbb2
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are other properties of cancer cells?

A
  • Altered cellular function
  • Abnormal morphology
  • Cells are capable of independent growth
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How is cellular function altered in cancer cells

A
  • Loss of cell-to-cell adhesion
  • Altered cell-to-matrix adhesion
  • Production of tumour-related proteins for example tumour biomarkers including Onco-foetal proteins, oncogenes, growth factors and receptors, immune checkpoint inhibitors
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are tumour biomarkers clinically used for?

A

Screening, diagnosis, prognosis, predictive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are examples of currently used tumour biomarkers? 1

A
  • Alpha fetoprotein
  • Carcino-embryonic antigen (CEA)
  • Oestrogen receptor
  • Prostate specific antigen
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the tumour biomarker alpha-fetoprotein used for?

A
  • Teratoma of testis

- Hepatocellular carcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the tumour biomarker Carcino-embryonic antigen (CEA) used for?

A

Colorectal cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the tumour biomarker Oestrogen receptor used for?

A

Breast cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the tumour biomarker Prostate specific antigen used for?

A

Prostate cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the morphology of cancer cells?

A
  • Cellular and nuclear pleomorphism- marked variation in size and shape
  • Mitoses are present and often abnormal
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is Angiogenesis?

A

New blood vessel formation by tumours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Why is angiogenesis important clinically?

A
  • Angiogenesis is required to sustain tumour growth
  • However, it provides a route for the release of tumour cells into circulation. More blood vessels in a tumour results in a poorer prognosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is apoptosis?

A

Programmed cell death which regulates tumour growth.

It is involved in response to chemotherapy and radiotherapy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How is the spread of cancer divided?

A

Divided into 2 parts- invasion (local) or metastasis (spreads to other tissues/organs)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What will a secondary tumour look like?

A

Identical to primary tumour

17
Q

How can a tumour spread be described?

A

Normal> Tumour> Metastasis

18
Q

What does metastasis involve?

A
  • Increased matrix degradation by proteolytic enzymes

- Altered cell-to-cell and cell-to-matrix adhesion

19
Q

What are the modes of the spread of cancer?

A
  • Local spread
  • Lymphatic spread
  • Blood spread
  • Trans-coelomic spread
20
Q

How does tumour invasion occur?

A

Malignant tumour

Invasion into connective tissue

Invasion into lymph/blood vessels

21
Q

How does tumour invasion occur via lymphatics?

A
  • Adherence of tumour cells to lymph vessels
  • Invasion from lymphatics
  • Invasion from blood vessels
  • Invasion into tissue
  • Formation of metastasis
  • Clinical evidence of metastasis
22
Q

How does tumour metastasis occur via blood?

A
  • Adherence of tumour cells to blood vessels
  • invasion from blood vessels
  • invasion into tissue
  • formation of metastasis
  • clinical evidence of metastasis
23
Q

How does trans-polemic spread occur?

A

It is a special form of local spread.

-Spread of tumour cells across BODY CAVITIES e.g. pleural or peritoneal cavities

24
Q

What shows trans-polemic spread?

A

Tumours of lung, stomach, colon and ovary

25
What is the site of metastasis not related to?
Tissue blood flow
26
What does the site of tumour metastasis depend on?
Both tumour and tissue related factors
27
What are common site of metastasis?
Lung, liver, brain, bone, adrenal gland, peritoneum
28
What are uncommon site of metastasis?
Spleen, kidney, skeletal muscle, heart
29
What tissue do breast tumours common metastasise to?
Bone tissue
30
What tissue do prostate tumours common metastasise to?
Bone tissue
31
What tissue do colorectal tumours common metastasise to?
Liver tissue
32
What tissue do ovary tumours common metastasise to?
momentum/periotneum
33
What tumours can: - Kras - Braf - EGFR - PD-L1 - Her2 predict?
Kras- colorectal cancer Braf- melanoma EGFR- lung cancer PD-L1- lung cancer Her2- Breast cancer, gastric cancer