NEOPLASM Flashcards

1
Q

Neoplasia vs. Neoplasm

A
  1. new growth process
    Vs
  2. the growth
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2
Q

Differentiation vs. Proliferation

A
  1. determination of cell’s fate, specialization, the cell does not return back to its previous state
  2. cell division and growth of new cells
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3
Q

What are stem cells w/ potential for multiple different cellular outcomes?

spleen cell and a skin cell?

A

pluripotent cells

based on their morphology, intercellular characteristics, staining patterns in histology lab etc.

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4
Q

What can determines the kind of tumor you have

A

the differentiation state of the cell when it divides, or where it is in this process of development will determine the kind of tumor you will get if a mutation occurs in that cell.

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5
Q

What happens when differentiated cells mutate

A

differentiated tumors— benign tumors

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6
Q

What happens when undifferentiated cells mutate

A

form rapidly dividing tumors— malignant tumors

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7
Q

how checkpoints work in animal cells

A

Internal and external

cells generally have built-in stop signals until overridden by go-ahead signals

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8
Q

What events happen during the cell cycle?

A

1] Duplication of genetic material- more mistakes, lots of base pairs, prone to error
2] Alignment of chromosomes,
3] Cell division,
4] Pauses in cell cycle

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9
Q

Why are the pauses useful during the cell cycle?

A

serve as checkpoints, allow for monitoring duplication accuracy

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10
Q

What happens in G1 (gap 1) phases of the cell cycle

A

post-mitosi
cell growth phase
no DNA synthesis

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11
Q

What happens in S phase

A

DNA Synthesis

replication of DNA

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12
Q

What happens in G2 (gap 2) phase

A

no DNA synthesis the pre-mitosis phase

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13
Q

What happens in M phase

A

mitosis

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14
Q

What happens in G0 phase

A

quiescence, resting phase, coming out of the cycle

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15
Q

What are the function of CDK

A

Cyclin-dependent kinases, phosphorylation of enzymes

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16
Q

What are the function of cyclins

A

bind to CDKs
regulated by CDK inhibitors

cyclically proteins -increasing and decreasing concentration in the cell.

17
Q

What is the most important checkpoint for most cells and why?

A

**G1 checkpoint most important, “restriction point”.
If a cell receives a go-ahead signal at the G1 checkpoints, then divides
If it doesnt, it will switch into a non-dividing (arrested) - G0 phase

18
Q

What type of cells never divide and what organ will go back to the cell cycle?

A

Nerve and muscle cells

LIVER- Growth factors, cytokines, molecules d/t rauma bring the liver cells back for repair

19
Q

Why are cyclin-dependent kinases ?

A

w/in cell , cell cycle control molecules

Protein kinases -inactive form, go ahead fro mitosis

cyclin kinase that must be attached to a cyclin

20
Q

What is the go signal that moves a cell into mitosis?

A

Cyclin binding to Cdk to form MPF -maturing promoting factor . M-phase promoting factor of mitosis via phosphorlyation

moves the cell cycle into mitosis

21
Q

How does MPF turn off?

A

During anaphase, MPF helps switch itself off by initiating a process that leads to the destruction of its own cyclin.
Ending M phase

22
Q

How many Cdk proteins are involved in the G1 check point

A

at least 3 CDKs

many cyclins

23
Q

What is the suffix for benign tumor vs. malignant tumor?

A

oma vs. carcinoma

Glandular benign tumor is an adenoma
Glandular malignant tumor is an adenocarcinoma

24
Q

What characteristics make a tumor malignant?

A

1] proliferate to form new tissue, 2] do not wait for “go ahead” signals, 3] ignore “stop dividing” signals, 4] often do not mature normally (differentiate) to do the “job” the tissue is supposed to do, 5] do not die off (apoptosis) to keep the number of total cells constant

25
Q

Genes that turn off or decrease the rate of cell division classes of genes control checkpoints?

A

tumor suppressor genes- KEY p53

1] repair damaged DNA, 2] control the adhesion of cells to each other or to the extracellular matrix; proper cell anchorage is crucial in normal tissue, 3] components of cell signaling pathways that inhibit the cell cycle.

26
Q

Genes that turn on or increase the rate of cell division classes of genes control checkpoints?

A

proto-oncogenes KEY RAS

Code for
1] Growth factors and receptors
2]G proteins,
4] Enzymes that produce second messengers,
5] Genes that turn the production of these proteins on and off

27
Q

What mutated form of proto oncogen promote cancer?

A

oncogenes

28
Q

What is the incidence rate of mutation in ras and p53?

A

Mutation in Ras occurs in about 30% of human cancers,

Mutation in p53 in more than 50%- Li-Fraumeni syndrome-mutation of p53 on chromosome 17, high rate tumors

29
Q

What are the 3 ways that the p53 protein prevents damaged DNA from passing on?

A

1] blocks the ability of cyclins,
2] can directly turn on genes involved in DNA repair,
3] DNA irreparable, p53 activates “suicide” genes, whose protein products cause cell death by apoptosis.

30
Q

how p53 blocks the ability of cyclins?

A

p53 induces the expression of another gene called P21

31
Q

In addition to the preventing the passing of DNA, what other tumor suppressing function does p53 protein?

A

inhibits angiogenesis necessary for tumor development, target of cancer research

32
Q

Describe the function of tumor suppresor gene RB

A

Rb gene prevents the cell from entering S-phase until growth signals are present

33
Q

What does mutation of Rb gene on chromosome 13 result in?

A

Retinoblastoma, cancer of the retina

34
Q

Mutations of what genes would modify apoptosis?

A

1] bcl-2-preventing apoptosis
2] bax, bad, bcl-xS, bid, and p53-promoting apoptosis
3] c-myc- w/ p53 leads to apoptosis; w/ bcl-2 inhibits apoptosis

35
Q

What are telomeres?

A

DNA sequences at the ends of chromosomes where enzymes attach that duplicate DNA

telomeres do not get replicated w/ DNA

Division- loses length thus DNA damage

36
Q

What is transformation carcinogenesis?

A

process of going from non-malignant to malignant cell

Initiation- exposure, don’t know exactly when that happens

Promotin- induction of unregulated growth, formation of a tumor

Progression- tumor cells acquire malignant phenotype

37
Q

What type of cells do neoplasm often arise from

A

90% epithelium-Skin, respiratory tract, alimentary canal, surfaces of organs, colon, pancreatic, stomach, liver

10% mesenchymal-Muscle, bone

38
Q

Why are epithelium cells more likely to undergo neoplasia

A

1] It proliferates rapidly, so high turnover,

2] first to encounters environmental carcinogen