Cancer Flashcards

0
Q

what doe srenal mean?

A

kideny

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1
Q

What is metastasis?

A

When cancer cells are in the blood stream or lymph system.

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2
Q

what is the difference between benign and malignant tumors?

A

Benign: the structure of the organ is a typical structure, encapsulated, slow growth, no metasis.
Malignant: Atypical structure, locally invasive, rapid and erotic growth, metasis.

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3
Q

What is endriodemisis?

A

when cancer cells brind blood cells in to get nutrients

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4
Q

What is histology?

A

the microscopic study of biological material.

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5
Q

what are the three germ layers?

A

Ectoderm- outer layer
Endoderm- inner layer
Mesoderm- middle layer

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6
Q

what is the epithelium area?

A

comprised of cells that are from the endo- and ectoderm

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7
Q

what is the most common cancer class and why?

A

Carcinoma, because it is the cancer of skin tissue and that is the layer that comes into contact with everything increasing the chance of getting cancer.

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8
Q

What is Leukimia, Blastoma, enocarcinoma, and sarcoma?

A

Leukimia- cnacer in the blood system
Blastoma- orginates in the embryonic tissue
Enocarcinoma- originates in glandular tissue
Sarcoma- originates in connective tissue

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9
Q

What is teratoma?

A

has multiple tisse types

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10
Q

What is the grading part of cancer?

A

It is the degree of differentiation, Higher grade means leass degree wich is bad.
There are one through four grades

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11
Q

what is staging in cancer explain?

A

This is a system of TNM (tumors, lymph nodes and metasis)

There are stages for each category.

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12
Q

what are the staes of the cell cycle?

A

PPMAT

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13
Q

Describe what each stage of the cell cycle does ( includine in interphase)?

A

G1- Growth of the cell
S- synthesis of the DNA
G2- More growth and prep for mitosis
prophase- when the centrioles move to the poles of the cell and the mitotic spindle forms
prometaphase- the nuclear enevelope breaks down and the spindle connects to the centromere of the chromosome.
metaphase - chromosomes are lined up in the middle of the cell.
anaphase- the sister chromatids are seperated and move to opposite poles
telophase- the chromatid then reaches the pole and a nuclear enevelope forms around the DNA.
Cytokinesis- the cytoplasm splits and now there are two cells

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14
Q

what are the four checkpoints for the normal cell cycle? and how could these proteins cause a cell to turn cancerous?

A

RAD- checks to make sure the cell is big enough for cell division. If there are too many rad proteins the cell will just think that it is big enough an move on. Same case for if there are not enough
P53- Gardian of the genome, checks to make sure that all the DNA is correct.
ATM/nibrin- it makes sure the cell has replicated the DNA after S phase correctly.
MAD 1- During metaphase it checks to see if the chromatid are all lined up correctly.

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15
Q

what are quiescent cells?

A

cells that are in Gzero phase

16
Q

what is immunohistochemistry?

A

Acts as the ELISA test uses antibodies to detect specific antigens in cells of a tissue

17
Q

What is hyperpalasia?

A

when the cells in tissue grow in number

18
Q

what is hypertrophy/ Atrophy?

A

hyper- is when cells become too big

A- is whne cells become too small

19
Q

What is metaplasia?

A

the exchange of normal epithelium cells for another type of epi. cells.

20
Q

what is dysplasia?

A

it is a disordered growth and maturation of epithelium cells.

21
Q

what causes DNA damage?

A

UV rays
X rays
y-rays

22
Q

what are the two types of DNA damage?

A

Single-strand brreaks and double strand-breaks

23
Q

what problems could occur with double strand breaks?

A

Stalled replication
problems with transcription
loss or gain of chromatids or segments of chromatids

24
Q

what is chromosomal translocation?

A

when a part of a chromosome breaks off and is then placed on another chromose.

25
Q

how do our cells protect us from the sun?

A

Our cells have ways to protet and repair DNA:

physical protection- mechanism used by a cell to shield against things that are harmful to DNA.

26
Q

WHat is Melanin?

A

skin cell produce pigment to actually absorb some of the UV to protect our skin cells from getting damaged.

27
Q

what are the three steps of DNA repair?

A

1)Detection of damaged DNA
Transducers tell the effectors that there is a break
Effectors- tell the whole cell that there is DNA damage and activates DNA repair.
2)Checkpoint to allow for repair- Efffectors cause checkpoint activation.
3)Repair of the damaged DNA- after cell has arrested a checkpoint DNA repair will occur through a very complex process involving multiple proteins.

28
Q

what is Xeroderma Pigmentosa?

A

mutation that prevent DNA repair
prone to skin lesions
increased incidence of skin cancer like melanoma

29
Q

what are other mutations in DNA repairs that could cause disease?

A

NBS1- Njimejen Breakage Syndrome (NBS)
ATM- Ataxia Telangiectasia
p53-Li-fraumeni syndrome

30
Q

what is Mdm2 and Mdmx?

A

regulators that can control p53

31
Q

What is a comet assay?

A

A test to show how much damage is in the DNA by determining how far it travels?