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Issue 9, June 2002
The Viral Roots of Cancer
Reem Hasan
Biology, Georgetown University
hasan@jyi.org
When first confronted with the notion that
viruses can cause cancer, many individuals react with suspicion.
Traditionally, cancer is not thought of as an infectious disease;
rather, it is presumed to be a result of a genetic predisposition
to cancer, exposure to nuclear radiation or environmental toxins,
or unhealthy eating and exercise habits. Most people are familiar
with the widespread public health notices encouraging a healthy
lifestyle as a method for substantially decreasing the likelihood
that an individual will contract a serious illness such as cancer.
However, surprising as it may seem, viruses and other microbial
agents also have been correlated directly with a significant proportion
of cancer cases worldwide, according to prominent researchers in
the field. The human papillomavirus (HPV), for example, is a virus
that is implicated as a cause of cervical cancer. In contrast to
health-promoting behavioral choices, we may not have control over
exposure to the invisible cancer-causing viruses and microbial agents
that have been linked to cancer.
Viruses in Cancer Research
Viruses have
played an essential role in cancer biology research over the past
several decades. At first, viruses were utilized as valuable laboratory
research tools for understanding cell cycle controls and carcinogenesis,
the origins and development of cancer. The use of viruses allowed
researchers to unravel the genetics, mechanisms, and controls governing
the processes of normal cell growth and differentiation. Viruses
were also used to determine the role of aberrant cell growth or
proliferation - processes characteristic of cancerous tissues.
Early research on retroviruses - RNA viruses that insert themselves
into a host cell's DNA and then proliferate - allowed scientists
to identify various regions of the genome most susceptible to carcinogenic
mutations. Discovery of the "hot spots" of viral insertion led to
an understanding of the genomic areas that could produce cancer-like
replication rates of cells. Thus, in the research laboratory context,
viruses were beneficial tools that expanded the scientific community's
knowledge and understanding about basic mechanisms of normal and
cancerous cells.
Viruses do not play a carcinogenic role only in experimental studies,
however. The actual cancer-causing ability of some viruses has led
to research in viral oncogenesis, or the origins and development
of tumors. Cancer-causing viruses function much as non-carcinogenic
viruses do, invading the living cells of the host and using its
DNA-synthesizing proteins and mechanisms in order to produce more
copies of itself. Then, the virus disrupts an integral cell-cycle
control mechanism in order to render the infected cell and its progeny
cancerous, or "hyper-proliferative." Uncontrolled cell replication
or proliferation is the basis for oncogenesis.
Viruses and Cancer: The Case of HPV
There are variants
of HPV known to play significant roles in the origins of cervical
cancers, the second greatest cause of death in women due to cancer
worldwide. Normally, benign variants of HPV exist within the human
body, although the carcinogenic types are primarily spread through
sexual interaction with another infected individual. The genomes
of the harmful viruses contain different gene segments that code
for several factors. Two such factors, known as E6 and E7, play
roles in transforming the genes of the infected cell, effectively
"immortalizing" it. Immortalization, or abnormal cell life cycle
control involving continuous replication, is another way to describe
the primary characteristic of cancer development. When E2, an inhibitory
protein that usually keeps these factors under control, is rendered
nonfunctional by the integrating virus, the E6 and E7 segments cause
a transformation and proliferation of the infected cells and further
spread the virus.
This results in several functional and physical changes in the infected
cervical cells. As the layers of epithelium in the cervix mature
and move toward the surface, the virus proliferates within the cells
and is eventually expelled to the exterior as the cells reach the
epithelial surface. After this, the virus can infect other cells.
The effects of these viruses are manifested as lesions on the epithelial
surface, detected by the common clinical technique known as a Pap
smear.
In general, however, viruses have not been shown to be the sole
carcinogenic agents in an individual; in most cases, many patients
who are infected with viruses do not develop cancerous conditions.
Indeed, the human body hosts hundreds of different types of viruses,
and it is only in rare cases that this co-existent relationship
is disturbed, with severe results including cancer. For example,
the vast majority of people infected with HPV do not get cancer;
in fact, less that 0.1% of infected individuals develop tumors.
Often, viruses are able to generate their most serious effects in
individuals who are immuno-compromised or physiologically unable
to deter viral infection. According to Dr. Richard Schlegel, a scientist
at the Georgetown University School of Medicine, the viruses mainly
affect individuals who are unable to produce a cell-mediated response
to the antigens presented by the virus-infected cells. This distinction
likely plays a role in determining why the virus integrates into
the host cell genome in some individuals and does not do so in others.
Determining
the Role of Viruses
Because of these factors,
it is difficult to state, in terms of disease risk, that a virus is
the sole cause of the cancer development. Historically, to prove the
causality between a substance and a disease or other condition, Koch's
postulates must be satisfied. This task would involve isolating the
virus, growing it in a culture, and then inducing the cancer in an
animal and obtaining the same condition consistently under experimental
laboratory conditions (see side bar). Because the challenge of growing
certain viruses in a laboratory setting is great, this undertaking
can be
| Comparing
postulates: Is a virus the sole cause of cancer development? |
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Koch's Postulates:
- The
pathogen must be present in every case of the disease.
- The
pathogen must be isolated from the diseased host and
grown in pure culture.
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The specific disease must be reproduced when a pure
culture of the pathogen is inoculated into a healthy
susceptible host.
- The
pathogen must be recoverable from the experimentally
infected host.
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Hill's
modified postulates:
- Strength
of Association
- Consistency
- Specificity
- Temporality
- Biologic
gradient
- Biologic
plausibility
- Biologic
coherence
- Experimental
evidence
- Analogy
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more information on the epidemiological tenets of causality
and Hill's Postulates, click here.
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quite difficult. However, a more recent set of considerations formulated
by Hill can also be employed to assess the epidemiological
causality between the agent and the disease (see side bar). The criteria
tested include strength of statistical association, consistency, dose-response
relationship, coherence, specificity, and experimental evidence. Based
on these considerations, several viruses can be considered to be the
causal agents of various cancers. Epidemiological studies can be useful
in validating associations with risk of disease in a human population.
However, it is important to remember that while a virus may be implicated
as the primary causal factor behind a certain type of cancer, its
interaction and correlation with the presence or absence of other
substances is also a significant factor in determining the risk of
cancer development and its severity.
At present, more than 15 viruses have been shown to exist in a
causal relationship with cancer. The most prominent of these include
the Hepatitis B virus, Epstein-Barr virus, human papillomaviruses,
human T-cell leukemia virus type I, and hepatitis C virus, which
cause a variety of conditions, including liver, naso-pharyngeal,
cervical, and skin cancers. The hepatitis viruses are known to cause
80% of liver cancer cases worldwide, and the papillomaviruses are
responsible for the majority of cervical cancer cases. Overall,
some researchers estimate that 15% of incident cases worldwide are
in caused by viruses, and that of these cases, cancer appears to
be a side effect, or risk associated with the original viral infection.
HPV Vaccines
Worldwide, there
is a great deal of research currently in progress concerning the
prevention and treatment of cervical cancer. It is estimated that
about $6 billion is spent annually in the United States toward developing
and producing an effective vaccine on a mass scale. This large amount
of money is also the primary reason for the comparatively low cervical
cancer death rate in the United States; the combined effect of routine
screening and early treatment promotes greater survival.
In other areas of the world, the mortality associated with HPV infection
is much more serious, making it the primary cause of the 400,000
annual cervical cancer deaths worldwide. These nations lack the
resources to promote and implement a major screening program similar
to the program that exists in the United States.
Presently, a first-generation vaccine exists for HPV; however, at
approximately $100 per dose, it is inaccessible to residents of
most developing nations. To further complicate the problem, these
countries have the greatest need for the vaccines, as their prevention
guidelines are less ordered and systematic than the programs existing
in the United States and other developed countries.
Dr. Schlegel's laboratory at Georgetown University Medical Center
is involved in the development of a cheap and effective vaccine.
This vaccine is currently undergoing clinical trials to determine
its usefulness in humans. In previous trials on dogs, it has already
been shown as a protective factor against infection with the virus,
and a similar conclusion is expected in the human population.
Summary
Whereas the idea of
cancer-causing viruses may sound dubious at first, several viruses
do indeed play a significant role in the prevalence of cancer worldwide,
including HPV, Epstein-Barr virus, and Hepatitis B virus. Many of
these viruses are infectious, often spread through sexual contact
with another individual. However, they have their greatest effects
in immuno-compromised individuals, those who are unable to initiate
their cell-mediated immune responses, or are otherwise unable to effectively
fight off the infection even after identification of cancerous cells.
In developed nations, screening and other prevention techniques have
been used with great success to detect infections early, specifically
with regard to HPV. Cheap and effective vaccines are currently in
development for easy distribution worldwide, and this appears to be
a critical development for successful control of the spread of viruses
such as HPV and their associated cancers.
Suggested Reading
Butel
JS. "Viral carcinogenesis: revelation of molecular mechanisms and
etiology of human disease." Carcinogenesis: 21 (2000): 405-426.
Epidemiologic Tenets of Causality. Course Website, PH1820 - Statistical
Analysis Fall 2001, University of Texas School of Public Health. 2
May 2002. http://www.sph.uth.tmc.edu:8053/Biometry/LMoye/StatAnalysis%202001/PH1820%202001/epid1.htm
Schecter WP. "Human immunodeficiency virus and malignancy: thoughts
on viral oncogenesis". Archives of Surgery. 136 (2001): 1419-25.
Journal
of Young Investigators. 2002. Volume Five.
Copyright © 2002 by Reem Hasan and JYI. All rights reserved.
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