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The development of colorectal cancer is relatively well understood.Describe the steps of the development of colorectal cancer, including any genetic components.

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There can be a genetic basis to colon ca...

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Which of the following types of cancer is associated with a defect in nucleotide-excision repair?


A) Retinoblastoma
B) Xeroderma pigmentosum
C) Cervical cancer
D) Chronic myelogenous leukemia
E) Bloom syndrome

F) A) and E)
G) A) and C)

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What kind of enzyme phosphorylates other proteins, in turn either activating or inactivating the protein?


A) Cyclin
B) Cyclin-dependent kinases
C) Telomerase
D) GTPase
E) DNA polymerase

F) A) and B)
G) B) and D)

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List three ways in which proto-oncogenes can be converted to oncogenes by viruses.

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(1)The sequence of the proto-oncogene ma...

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Retinoblastoma (RB)protein is important in regulating the cell cycle.It must be completely phosphorylated before the cell can move from the G1 to the S phase of the cell cycle.Retinoblastoma is a type of cancer.Based on this information, what do you think goes wrong in retinoblastoma?

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Retinoblastoma is one example of several...

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How do we know that cancer is a genetic disease?


A) For all individuals that carry a cancer gene, cancer will develop in every tissue in the body.
B) Cancer is a leading cause of mortality worldwide.
C) Only cells exposed to chemical mutagens, but not ionizing radiation, will develop cancer.
D) Certain types of cancer often share the same chromosomal abnormalities.
E) All of the answers are correct.

F) A) and B)
G) A) and C)

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In Burkitt lymphoma, there is increased expression of the MYC gene.Which of the following BEST explains this situation?


A) A chromosome deletion has removed a tumor-suppressor gene.
B) A chromosome deletion has removed an oncogene.
C) There is a chromosome duplication that involves a segment with an oncogene.
D) A translocation has brought the MYC gene next to a different regulatory region.
E) The MYC gene has been amplified.

F) C) and D)
G) A) and B)

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Explain how DNA sequencing studies can aid in our understanding of cancer formation.

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DNA sequencing technology has been used ...

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Explain briefly why changes in oncogenes result in more rapid progression of a cancer compared to changes in tumor-suppressor genes.Mention one situation in which changes in a tumor-suppressor gene have a similar likelihood of causing cancer as changes in an oncogene.

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A single mutation in DNA is sufficient t...

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Many viruses that are associated with cancers in animals are _____ that use reverse transcriptase.


A) papilloma viruses
B) Epstein-Barr virus
C) retroviruses
D) hepatitis B virus
E) None of the answers is correct.

F) B) and D)
G) A) and C)

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The increased levels of telomerase associated with many tumor cells likely promotes cancer by:


A) enhancing levels of DNA repair so that cells remain normal and have stable genomes and thus would be able to replicate their DNA and divide more often.
B) promoting the efficiency of the spindle-assembly checkpoint.
C) reducing the expression of several oncogenes.
D) allowing cells to continue to divide when, normally, chromosomes should shorten beyond a point where division would be no longer possible.
E) decreasing the number of epigenetic changes that would promote cancer.

F) C) and D)
G) B) and D)

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What are oncogenes and tumor-suppressor genes? How are they involved in carcinogenesis?

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The control of the cell division cycle i...

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How can defects in DNA-repair mechanisms lead to the development of cancer?

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Defects in DNA-repair mechanis...

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Which of the following BEST characterizes many cancers such as colorectal cancer?


A) They result from the activation of one critical tumor-suppressor gene.
B) They result when the transition from G2 to M in the cell cycle is inhibited.
C) They result when DNA replication during the S period of the cell cycle is inhibited.
D) They result from a series of sequential mutations in a number of genes.
E) They result from decreased expression in a series of cellular oncogenes.

F) A) and B)
G) B) and D)

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Briefly describe the relationship among cyclins, cyclin-dependent kinases (CDKs), and cancer.

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Cyclins and CDKs play critical roles in ...

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Which of the following statements is TRUE concerning the function of proto-oncogenes?


A) They make products that act as signals to initiate cellular apoptosis.
B) Their products are components of cell growth.
C) Proto-oncogenes make products that act as cell checkpoint regulators.
D) Proto-oncogenes make products that scan the genome for DNA damage.
E) Proto-oncogenes make products that repair DNA at sites of lesions.

F) B) and D)
G) B) and E)

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Which of the following occurs in familial retinoblastoma?


A) There are two subsequent gametic mutations in Retinoblastoma (Rb) gene.
B) A single mutation in the Retinoblastoma (Rb) gene leads to the loss of heterozygosity.
C) Tumors develop only after exposure to ionizing radiation.
D) Changes in the cytoskeleton lead to mutations in the Retinoblastoma (Rb) gene.
E) Multiple gametic cells mutate all at once.

F) C) and D)
G) C) and E)

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Which of the following is NOT correct?


A) Mutations in oncogenes often act in a dominant manner.
B) Mutations in tumor-suppressor genes often act in a recessive manner.
C) In cancer, tumor-suppressor genes often convert to oncogenes following exposure to mutagens.
D) Normal action of proto-oncogenes is to stimulate cell proliferation.
E) All of the answers are correct.

F) A) and B)
G) A) and E)

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The Philadelphia chromosome is:


A) an example of an aneuploidy.
B) the result of a translocated chromosome involving parts of chromosomes 9 and 22.
C) a lengthened version of chromosome 22 that results from a recombination event with chromosome 12.
D) a shortened version of chromosome 22 that results from a deletion.
E) a lengthened version of chromosome 22 that results from a duplication.

F) A) and D)
G) B) and D)

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Deletions of what categories of genes are likely lead to cancer?


A) Tumor suppressors
B) Proto-oncogenes
C) Growth factors
D) All of the answers are correct.
E) None of the answers is correct.

F) All of the above
G) B) and C)

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