oncology - patho E4 Flashcards

1
Q

the parts of the cell cycle

A

stage G0
stage G1
Stage S
Stage G2
Stage M

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2
Q

cell cycle: G0

A

The cell is at rest and is not actively engaged in the cell cycle.

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3
Q

cell cycle: G1

A

Cells enter the cell cycle and prepare for deoxyribonucleic acid (DNA) replication. Proto-oncogenes, genes that control cell replication, are activated.

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4
Q

cell cycle: S

A

Synthesis of structures occurs and the structures move to opposite poles in preparation for division into two separate cells. The 46 chromosomes reorganize as two separate sets of 23 chromosome pairs arranged at opposite poles. Two nuclear membranes develop around the two separate sets of 23 pairs.

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5
Q

cell cycle: G2

A

Cells prepare to divide

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6
Q

cell cycle: M

A

Mitosis is completed and two daughter cells are created

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7
Q

compared to a normal cell cycle, what does a cancer cell cycle not have

A

-a rest phase (G0) -> rapidly reproduction
-check points to make sure everything is normal and correct -> allows for lots of cell changes (no DNA errors recognized, no apoptosis)

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8
Q

the goal of cancer treatment drugs is to do what

A

impact the cell cycle

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9
Q

what do cancer cell disregard

A

the growth inhibitors released by neighboring cells -> as they proliferate, they accumulate on top, around & besides each other, take over boundaries of organs, crowd out normal cells and may even breakfree and travel to distant body sites

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10
Q

immune surveillance

A

our immune system recognizes abnormal cells as “non self antigens” -> when discovered the immune system initiates an attack to destroy the substance
with age, this weakens -> increased risk of tumor development

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11
Q

differentiation

A

refers to the extent that neoplastic cells resemble normal cells both structurally and functionally
Lack of differentiation is called anaplasia, a term that indicates total cellular disorganization, abnormal cell appearance, and cell dysfunction

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12
Q

what does it mean when someone says “the cancer cell is well differentiated”

A

the cancer cell closely resembles & functions like the cell of origin

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13
Q

do benign tumors tend to be more differentiated or anaplastic

A

well differentiated -> remain localized, don’t break away, do not invade and destroy surround tissues

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14
Q

do malignant tumors tend to be more differentiated or anaplastic

A

anaplastic (or poorly differentiated)

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15
Q

review cancer cells break rules chart & differences between normal and cancer cells

A
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16
Q

tumor markers: what are they

A

biologic substances that some tumors put off that can be measured

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17
Q

tumor markers: what type of substances

A

hormones
enzymes
antigens
genes

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18
Q

tumor markers: where can they be found

A

blood
urine
cerebral spinal fluid
tumor plasma membrane

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19
Q

tumor markers: what are they used for

A

screening or diagnostic
can help us follow the clinical course of the cancer during treatment

20
Q

tumor markers: are they diagnostic of cancer

A

not always but can help diagnose specific types of cancers

21
Q

examples of tumor markers:

A

prostate specific antigen
BRCA gene mutation
can be elevated with benign tumor

22
Q

maligant tumor grading

A

Grade I: cells are well-differentiated
Grade II: cells are moderately differentiated
Grade III: poorly differentiated or anaplastic cells

23
Q

Staging classifies the tumor according to size, invasiveness, and spread using a TNM system:

A

T - tumor size, location, and involvement.
N - lymph node involvement.
M - metastasis to distant organs.

24
Q

review TNM classification system

A

needs a biopsy

25
Q

four stage classification system

A

doesn’t give much info, better for gen pop
Stage 1: Confined to organ of origin
Stage 2: Locally invasive
Stage 3: Regional spread
Stage 4: Spread to distant sites

26
Q

four phases of carcinogenesis

A

initiation
promotion
progression
metastasis

27
Q

what is involved in carcinogenesis

A

genes
carcinogens
promoters

28
Q

carcinogenesis: intitation

A

the alteration, change or mutation of genes that arise spontaneously or induced by exposure to a carcinogenic agent

29
Q

carcinogenesis: promotion

A

actively proliferation cells accumulate
reversible with chemotherapy

30
Q

carcinogenesis: progression

A

when cells undergo further mutation & these cells tend to be more invasive with metastatic potential

31
Q

carcinogenesis: metastasis

A

the spread of cancer

32
Q

what are the two major classes of cancer genes

A

1) tumor suppressor genes (“car break doesn’t work” -> these cells are inactivated & nothing stops the proliferations of mutated genes and nothing tells the cell when to die)
2) oncogenes (“gas pedal controlling speed” -> mutated proto-oncogenes are permanently turned on and cells can keep dividing out of control)

33
Q

how to classify carcinogens

A

-known (smoking, alc, HPV, HIV)
-probable (night shift), evidenced based
-possible (engine exhaust), insufficient evidence

34
Q

what is a promoter

A

an agent that help the mutated gene proliferate
ex: high fat diet, alc, tobacco, hormones

35
Q

viral induced cancer

A

certain malignancies are associated with cancer inducing viruses (like hiv)
MOA: always involve the activation of growth promoting pathways or inhibition of tumors suppressors in infected cells

36
Q

how do tumors create their needed blood supply

A

they secrete vascular endothelial growth factor, a substance that gives them the capability to develop new blood vessels

37
Q

with cancer spread we can have:

A

seeding
implantation
metastasis

38
Q

cancer spread: seeding

A

the tumor erodes and sheds into the body cavities -> the “seed” can be planted in different body cavities

39
Q

cancer spread: implantation

A

refers to the direct expansion of the tumor to an adjoining tissue -> prostate is right next to bladder so the prostate cancer grows right into the bladder

40
Q

cancer spread: metastasis

A

2 primary routes are lymphatic & vascular
when the cancer moves to distant sites through the lymph or vas system

41
Q

lymphatic spread

A

the first stop is the lymph system & get trapped in the lymph leading to:
1) cell death in the lymph
2) cells can go dormant in the lymph
3) flourish / proliferate
if they survive then they can start traveling around the entire lymph system

42
Q

vascular spread

A

cancer cells can penetrate blood vessels that drain the tumor site and once they get into circulation, they can deposit anywhere
first stop is often the liver

43
Q

common metastatic sites for tumors: lung

A

bone, brain

44
Q

common metastatic sites for tumors: colon

A

liver

45
Q

common metastatic sites for tumors: breast

A

bone, brain, liver, lung

46
Q

common metastatic sites for tumors: prostate

A

vertebrae

47
Q

common metastatic sites for tumors: melanoma

A

brain