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A) clonal evolution.
B) metastasis.
C) loss of heterozygosity.
D) epigenetic evolution.
E) signal transduction.
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A) Duplications; deletions
B) Inversions; translocations
C) Duplications; inversions
D) Deletions; translocations
E) Aneuploidy; deletions
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A) proto-oncogenes
B) tumor-suppressor genes
C) genes that promote angiogenesis
D) genes that allow the G1/S transition
E) genes involved in DNA repair
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A) oncogenesis
B) angiogenesis
C) malignancy
D) secondary tumorigenesis
E) metastasis
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A) A chromosome deletion has removed a tumor-suppressor gene.
B) A chromosome deletion has removed an oncogene.
C) A chromosome duplication 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.
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A) a drug that increases the levels of telomerase expression
B) a drug that methylates the promoter of the telomerase gene
C) a drug that repairs the mutation within the coding region of the telomerase
D) a drug that allows the telomerase to be expressed but at lower levels
E) a drug that inhibits a tumor-suppressor gene in the cell line
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A) initiating mitosis.
B) controlling cell adhesion.
C) opening ion channels.
D) duplicating the centrosome.
E) preventing aneuploidy by regulating the spindle-assembly checkpoint.
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A) proto-oncogenes.
B) tumor-suppressor genes.
C) passenger genes.
D) inhibitor genes.
E) driver genes.
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A) errors in transcription
B) the production of unbalanced gametes because of nondisjunction during meiosis
C) genetic or epigenetic changes in somatic cells
D) delayed cell division during early embryogenesis
E) No correct answer is provided.
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Multiple Choice
A) a mutation that causes the overexpression of a DNA repair gene
B) a mutation that causes telomerase to have reduced expression in somatic cells
C) a deleterious mutation in one copy of a tumor-suppressor gene
D) a deletion that removes one copy of an oncogene
E) an extra X chromosome from the mother
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A) Binding of the growth factor to the receptor would occur, but the receptor's conformational change that is needed for the pathway to go forward would not occur.
B) Activated Ras would no longer have the ability to activate Raf, and the signal-transduction pathway would be halted at this step.
C) Ras would lose the ability to bind GTP and thus could no longer become activated, and the signal-transduction pathway would be halted at this step.
D) MAP kinase would not be activated and thus could not move into the nucleus to activate transcription factors.
E) Inactive Ras would move into the nucleus and inactivate tumor-suppressor transcription factors, which could ultimately result in cancer.
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A) inducing the increased expression of a tumor-suppressor gene
B) inducing the increased expression of DNA-repair genes
C) promoting a decreased level of telomerase activity
D) inhibiting the G1 to M transition in the cell cycle
E) increasing the expression of an oncogene
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