Cancer Rehabilitation Flashcards

1
Q

What are some non-modifiable risk factors for cancer?

A
Age 
Genetics 
Epigenetics 
Immunosuppression 
Radiation 
Sunlight
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2
Q

What are modifiable risk factors for cancer?

A
Alcohol 
Cancer causing substances 
Chronic inflammation 
Diet
Hormones 
Immunosuppression 
Infectious agents 
Obesity 
Radiation
Sunlight
Tobacco
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3
Q

What is proliferation for normal cell characteristics?

A
  • increase in cell number
  • regulated by growth factors
  • Cells go through cycle (controlled by cell inhibitor, to prevent excessive growth)
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4
Q

What is differentiations for normal cell characteristics?

A
  • Cells become “Specialized” to carry out particular functions (specific structure and function)
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5
Q

What limits the # of cell divisions?

A

Dictated by telomeres

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6
Q

What is contact inhibition?

A

When cells touch each other, shut off

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7
Q

Describe carcinogenesis and what it breaks down into? (2 parts)

A

Can lead to genetic alterations or epigenetic alterations

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8
Q

What are genetic alterations from carcinogenesis?

A

Point mutation
SNP
Copy # variants (loss of heterozygozity (LOH), homo deletion, gain copy #)

ALL leads to STRUCTURE changes

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9
Q

What are epigenetic alterations from carcinogenesis?

A

Micro RNA
DNA methylation
Histone Modifications (acetlyation, methylation, sumolation, ubiquination, phosphorlyation)

All lead to FUNCTION changes

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10
Q

What is a tumor?

A

Abnormal mass of tissue that results when cells divide more than they should or do not die when they should. May be benign or malignant. Also called neoplasm

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11
Q

What are the cellular or tumor characteristics of cancer? (3)

A
  1. Abnormality
  2. Uncontrollability
  3. Invasiveness
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12
Q

Describe the types of carcinogenic drivers

A
  • Proto-oncongene
  • Oncogene
  • Tumor suppressor gene
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13
Q

What is a Proto-onconogene?

A

A gene involved in normal cell growth (regulation in a normal cell cycle)
Mutations may cause it to become an oncogene, which cause the growth of tumor cells

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14
Q

What is an oncogene?

A

Mutated proto-onconogene

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15
Q

What does a tumor suppression gene do?

A
  • negative regulator of growth factor stimulation
  • controls cell growth and division
  • Suppress or block the development of cancer
  • Anti-onconogene
  • activation or mutation of tumor suppressor genes results in carcinogenesis
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16
Q

How do you find the prevalence of a disease? Difference between point and period prevalence?

A

of cases / everyone at risk for a disease

Point prevalence - Count only those alive in particular date in time

Period prevalence - counts all cases including new cases and dates between 2 dates (BETTER MEASURE OF THE DIEASE LOAD)

17
Q

What is the difference between prevalence and incidence rates?

A

Prevalence = All cases

Incidence rates = New Cases
- Frequency of occurrence of NEW cases of disease or injury in a population over a specific period of time

18
Q

What are the most common cancers in the world?

A
Prostate & Breast cancer 
Colorectal (2nd most consistent for death)
Lung (most consistent for death) M/F 
Stomach 
Corpus uteri 
Bladder
Cervix
Liver
Thyroid
19
Q

What is the Mortality Rate? What is the denominator

A

Frequency of occurrence of death in a defined population during specified interval

Denominator = Avg population

20
Q

What are the 2 cancers with most death for men and women?

A

Male: Lung + Colon + Prostate

Women: Lung + breast + colon

21
Q

What are the most common cancers for children and when are they usually diagnosed?

A
  • Acute Lymphocytic leukemia (ALL)
  • Brain and other CNS tumors
  • Neuroblastoma

Avg age Dx: 6 years

22
Q

What are the high risk populations for cancer?

A
  • Heavy Alcohol use
  • Older Adults (cancer is aging disease) #1 risk factor
  • Exposure to cancer causing substances
  • Obese persons BMI > 30
  • high inflammatory dietary habits
  • Cancer survivors
  • Radiation exposure + treatment
  • Persons w/ immunosuppression
  • Exposure to tobacco or smoke
23
Q

What should women and men get screened for breast/prostate cancer?

A

Breast: age 50-74 biennial screening
Prostate: 55-69 years old PSA

24
Q

What should a person get screened for lung cancer?

A

Low dose computed tomography smoked in age 55-80 who have 30 year smoking and currently smoke or have quit in the past 15 years

25
Q

Describe the primary, secondary, and tertiary prevention strategies

A

Primary: prevent the disease
Secondary: detect the disease early
Tertiary: Reduce symptoms and improve QoL

26
Q

What is Caution - P

A

Change in bowels/bladder = Ultrasonography and endoscopy

A sore that doesnt heal = biopsy and oral/skin examination

Unusual bleeding = rectal exam/gynaec exam

Thickening or lump in breast/testicles/elsewhere = Ultrasonography and FNAC

Ingestion or difficulty swallowing = Endoscopy

Obvious change in size of mole = biopsy

Nagging cough = ENT exam

Pain = nocturnal pain, different times,/types, headache in am but improves

27
Q

Describe Benign staging

A
Slow growing
Localized
Not invasive 
Not cancerous
Recurrence unlikely
Encapsulated
End with OMA 

In capsule

28
Q

Describe malignant staging

A
Rapid/slow growth 
Invasive
Encapsulated 
Cancerous 
Possible recurrence 
End in Oma  (SARCOMA)

Malignant tumors = Capsule is gone and breaks out for invasion

29
Q

What are characteristics of malignant tumors?

A
no normal cell organization/differentiation 
Lack control of cell division 
No contact inhibition 
Do not adhere to each other (break loose from mass- invades other tissues and spreads) 
Do not undergo apoptosis 
Abnormal cell membranes
Altered surface antigens 
Compress blood vessels
30
Q

Describe Angiogenesis in cancerl cells

A

Development of new capillaries (vascular endothelial growth factor - VEGF) for cancer survival

Secretion of matrix metalloproteinase (MMP)- Collagenase (breaks down collagen in ECM)

31
Q

Describe the diagnosis of cancer

A
  • Site: Primary (orgin), secondary - metastasis
  • Palpable mass or lump
  • Biopsy
  • Imaging technologies
  • histology
  • Tumor markers
  • Grading
  • Staging
32
Q

Explain the histological grading (general)

A

GX: cannot be assessed (undetermined grade)
G1: Well differentiated (low grade)
G2: Moderately differentiated (intermediate)
G3: Poorly differentiated (high grade)
G4: Undifferentiated (high grade)

33
Q

Explain Primary tumor grading (TNM system)

A

TX: primary tumor cannot be evaluated
T0: No evidence of primary tumor (GOOD)
Tis: carcinoma in situ (well contained)
T1,2,3,4: Size and/or extend of tumor

34
Q

Explain Regional Lymph nodes (TMN system)

A

Nx: cannot be evaluated
N0: no regional lymph node involvement (good)
N1,2,3: degree of involvement # and location

35
Q

Explain distant metastasis

A

Mx: cannot be evaluated
M0: no distant metastasis
M1: Distant metastasis is present

36
Q

Explain cancer staging

A

0: carcinoma in situ
1: early stage, localized to the primary organ
2: increased risk of regional spread
3. local cancer has spread regionally
4: metastasis

37
Q

How do malignant tumors spread?

A

Invasion: local spread to adjacent tissues and destroy

Metastasis: spread to distant sites via blood/lumph

Seeding (implantation) - another form of mets, distant stites, via other body fluids or along membranes

38
Q

What are the most common sites for mets?

A

Bone, Liver, Lung

39
Q

What are the 3 types of breast biopsies?

A
  1. fine needle (sample of cells)
  2. Core needed w/ US or MRI for guide
  3. Open (surgical) biopsy