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
Q

What does the translocation of the philadelphia chromosome cause?

A

A fusion gene/protein
between the BCR gene and the ABL gene

26
Q

What is the fusion protein in a philadelphia chromosome?

A

Tyrosine kinase

27
Q

What is the parent drug used to treat CML?

A

Gleevec (imatinib)

28
Q

What is the mechanism of action WITHOUT Gleevec to induce leukemia?

A

BCR-ABL active -> signal for cell proliferation and survival -> leukemia

29
Q

What is the mechanism of action of Gleevec to NOT induce leukemia?

A

BCR-ABL blocked with gleevec -> no signal -> no leukemia

30
Q

What are the treatment phases for leukemia?

A
  1. induction therapy
  2. consolidation/intensification therapy
  3. maintenance therapy
31
Q

What is the goal of induction therapy?

A

Kill the leukemia cells in the blood and bone marrow
This puts the leukemia into remission

32
Q

What is the goal of consolidation therapy?

A

Kill any remaining leukemia cells that may not be active but could begin to regrow and cause a relapse

33
Q

What is the goal of maintenance therapy?

A

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
Q

Where does acute lymphoblastic leukemia start?

A

Lymphoid cells of the bone marrow

35
Q

What occurs in lymphoblastic leukemia?

A

Bone marrow produces too many immature lymphocytes

36
Q

What are risk factors of ALL?

A
  • 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
Q

What are possible signs and symptoms of ALL?

A

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
Q

What is the diagnosis of ALL?

A

Blood CBC (complete blood count), bone marrow analysis, cytogenetic analysis

39
Q

What is ALL prognosis?

A
  • 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
Q

What are low risk ALL groups?

A

Includes children aged 1 to
younger than 10 years who have a WBC count of less
than 50,000/μL at diagnosis

41
Q

What are high risk ALL groups?

A

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
Q
A