Devita, Hellman, and Rosenberg's Cancer

(Frankie) #1

LWBK1006-03 LWW-Govindan-Review November 24, 2011 11:19


48 DeVita, Hellman, and Rosenberg’s CANCER: Principles and Practice of Oncology Review

genes, which then can lead to devastating consequences resulting in dis-
tinct outcomes in distinct tissues. The haploinsufficient tumor suppressors
contrast with the retinoblastoma paradigm or the Knudson’s hypothesis.
In retinoblastoma, individuals inherit a mutation in one of the alleles of
the RB gene and require a “second hit” to the other allele to develop
cancer.

Answer 3.20. The answer is A.
Among the animal viruses, retroviruses are unique in having an RNA
genome that replicates through a DNA intermediate. Once the retrovirus
infects the cell, the single-stranded viral genome is converted to double-
stranded DNA by an RNA-dependent DNA polymerase or reverse tran-
scriptase. The double-stranded DNA then is integrated into a host cell
chromosome. Retroviruses in animals can transform the infected cell by
integrating the viral DNA close to cellular oncogenes, integrating a pro-
tooncogene in the host cell genome, or altering the cellular gene expres-
sion or function. In humans, HTLV1 is the only retrovirus that has been
shown to have a direct transforming effect. HIV, the other retrovirus,
is more likely to cause malignant transformation in humans through an
indirect effect of immune suppression.

Answer 3.21. The answer is D.
Retroviruses transform cells through either an acute process or a slow
transforming process. Acutely transforming viruses insert a viral oncogene
into the host cell genome leading to malignant transformation. The slowly
transforming viruses cause cellular transformation either by inserting the
viral DNA adjacent to a cellular protooncogene (insertional mutagenesis)
or altering the expression of cellular gene expression and function by
viral proteins. Inflammation and its consequences are not known to be
an important cause of retrovirus-induced cellular transformation.

Answer 3.22. The answer is A.
HTLV-1 shares a number of features with HIV: a complex genetic struc-
ture, tropism for CD4 T lymphocytes, induction of syncytia in cultured
T cells, and similar routes of transmission (blood transfusions, sexual con-
tact, needle sharing, and breastfeeding). However, HTLV-1 infection is not
associated with marked cellular immunodeficiency unless ATL develops.
Unlike HIV, where infection by free virions is typical, with high levels
of viremia detected in HIV-1-infected individuals, a significant viremia is
not detected in individuals with HTLV-1. In patients with HTLV-1, the
virus spreads to uninfected cells by cell-to-cell transmission of the virus.
In addition, the number of HTLV-1-infected cells within an individual
increases by simple mitosis of virus-containing T cells.

Answer 3.23. The answer is C.
HTLV1 protein Tax activates viral gene expression by interacting with cel-
lular transcription proteins. Subsequently through this interaction with
cellular transcription proteins, Tax leads to activation of several cellular
Free download pdf