11/2: Anticancer Therapies: Radiation and Drugs Flashcards

1
Q

What are key properties of cancer cells?

A
  • They reproduce without regard to the normal restraints on cell
    growth and cell division
    – They invade and colonize areas normally reserved for other cells
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2
Q

What are abnormal cells that grow (increase in mass) and proliferate (divide)?

A

Tumors or neoplasms

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3
Q

When are tumors considered benign?

A

If the neoplastic cells do not
become invasive

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4
Q

When are tumors considered cancerous?

A

If it acquires the ability to invade surrounding tissue at which point it is has become malignant

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5
Q

Malignant tumors often, as a consequence of
their invasiveness, produce cells that break
out of their primary site and form secondary
tumors at other sites called…

A

Metastases

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6
Q

Is a single mutation sufficient to cause cancer?

A

No - inherited mutations offer increased risk

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7
Q

What are potential risk factors for cancer?

A

– Radiation exposure
– UV light from the sun
– Chemicals (carcinogens)
– Life-style (smoking, certain diets)
– Viruses (EBV, HIV, HPV)

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8
Q

The overall incidence of cancer increases with ______

A

age

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9
Q

During the cell-cycle, the cell has scanning mechanisms to do what?

A

Detect DNA damage and either repair the damage or result in cell-cycle arrest or cell death (apoptosis)

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10
Q

What protein is a key mechanism in the cellular response to DNA damage?

A

p53

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11
Q

What is the basic strategy for treating cancer?

A

To induce so much damage to
the tumor cells via DNA damage (primarily) to
prevent them from dividing and induce cell death

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12
Q

What are the types of radiation therapy?

A

External beam therapy
Internal Radiation therapy
Photon Therapy
Charged particle or proton therapy

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13
Q

What therapy uses a machine to send high energy beams from outside the body to the tumor area?

A

External beam therapy

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14
Q

What therapy uses radioisotope given internally, radiation generally only travels a short distance depending upon the isotope and its energy?

A

Internal radiation therapy

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15
Q

What therapy works either by direct ionization of atoms in the DNA chain or indirectly by ionization of water to form hydroxyl radicals that can then damage DNA?

A

Photon therapy

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16
Q

What therapy uses a particle accelerator to beam high-energy particles (protons or carbon, boron or neon nuclei). Better ability to precisely localize the radiation
dosage and less damage to surrounding, healthy tissue?

A

Charged particle or proton therapy

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17
Q

How does doxorubicin hydropcholride (adriamycin) work?

A

Intercalates between base pairs in the DNA helix,
thereby preventing DNA replication and ultimately inhibiting protein synthesis

18
Q

How does bleomycin sulfate work?

A

forms complexes with iron that reduce molecular oxygen to superoxide and hydroxyl radicals which cause single- and double-stranded breaks in DNA

19
Q

How does cisplatin work?

A

inducing intrastrand and interstrand DNA cross-links, as well as DNA-protein cross-links, which induce apoptosis

20
Q

How does methotrexate work?

A

Inhibition of DNA and RNA syntheses

21
Q

How does vinblastine work?

A

inhibits microtubule formation, resulting in disruption of mitotic spindle assembly and arrest of tumor cells

22
Q

What is a treatment designed to induce, enhance or suppress the immune response. Most applications are designed to stimulate a person’s own immune response to destroy cancer cells that have escaped normal immune surveillance?

A

Immunotherapy

23
Q

What is leukemia characterized by?

A

Increased production/growth of granulocytes in the bone
marrow that then circulate in the blood

24
Q

What is leukemia caused by?

A

A chromosomal translocation called the Philadelphia chromosome

25
What does the translocation of the philadelphia chromosome cause?
A fusion gene/protein between the BCR gene and the ABL gene
26
What is the fusion protein in a philadelphia chromosome?
Tyrosine kinase
27
What is the parent drug used to treat CML?
Gleevec (imatinib)
28
What is the mechanism of action WITHOUT Gleevec to induce leukemia?
BCR-ABL active -> signal for cell proliferation and survival -> leukemia
29
What is the mechanism of action of Gleevec to NOT induce leukemia?
BCR-ABL blocked with gleevec -> no signal -> no leukemia
30
What are the treatment phases for leukemia?
1. induction therapy 2. consolidation/intensification therapy 3. maintenance therapy
31
What is the goal of induction therapy?
Kill the leukemia cells in the blood and bone marrow This puts the leukemia into remission
32
What is the goal of consolidation therapy?
Kill any remaining leukemia cells that may not be active but could begin to regrow and cause a relapse
33
What is the goal of maintenance therapy?
Kill any remaining leukemia cells that may regrow and cause a relapse *cancer treatments are given in lower doses than those used for induction and consolidation therapy
34
Where does acute lymphoblastic leukemia start?
Lymphoid cells of the bone marrow
35
What occurs in lymphoblastic leukemia?
Bone marrow produces too many immature lymphocytes
36
What are risk factors of ALL?
* Being exposed to x-rays before birth. * Being exposed to radiation. * Past treatment with chemotherapy. * Having certain changes in the genes. * Having certain genetic conditions that include the following: – Down syndrome, Ataxia telangiectasia, Bloom syndrome, Neurofibramatosis, Schwachman Syndrome
37
What are possible signs and symptoms of ALL?
Fever; foul smelling urine; easy bruising or bleeding; petechiae (flat, pinpoint, dark- red spots under the skin caused by bleeding); bone or joint pain; painless lumps in the neck, underarm, stomach or groin; pain or feeling of fullness below the ribs; weakness, feeling tired, or looking pale; loss of appetite
38
What is the diagnosis of ALL?
Blood CBC (complete blood count), bone marrow analysis, cytogenetic analysis
39
What is ALL prognosis?
* Age at diagnosis, gender, and race. * The number of white blood cells at diagnosis. * Whether the leukemia cells began from B lymphocytes or T lymphocytes. * Whether there are certain changes in the chromosomes of lymphocytes. * Whether the child has Down syndrome. * Whether the leukemia has spread to the brain, spinal cord or testicle. * How quickly and how low the leukemia cell count drops after initial treatment.
40
What are low risk ALL groups?
Includes children aged 1 to younger than 10 years who have a WBC count of less than 50,000/μL at diagnosis
41
What are high risk ALL groups?
children younger than 1 year or 10 years and older and children who have a white blood cell count of 50,000/μL or more at diagnosis
42