Colon Cancer and Genetic Testing

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Colon Cancer and Genetic Testing


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  1. Colorectal (Colon) Cancer Slideshow Pictures
  2. Digestive Disease Myths Slideshow Pictures
  3. Medical Illustrations of Colon Cancer Collection

Medical Author: Jay W. Marks, MD

Medical Editor: Michael Lill, MD

How is genetic testing for colon cancer risk done?

There has been much excitement during the past decade because of the
identification of abnormal or defective genes (mutations) associated with
colon cancer
in families where colon cancer is common. When a defective gene can be
identified, it is possible to examine other members of the family to see if they
also carry the defective gene. Those individuals who carry the defective gene
are at a very high risk (75%-100%) for developing colon cancer. The reason for
the excitement is that if an individual is found to have the defective gene, his
or her colon can be carefully monitored and then removed before the cancer occurs.

Only 5% of all colon cancers occur in families with a history of colon cancer
and identifiable genetic defects. Therefore, genetic testing as it exists today
is useful for only a minority of the about 130,000 people each year who are destined
to develop colon cancer. Nevertheless, genetic testing is important because the
risk is so extremely high among individuals who are found to have the genetic
defect. In addition, more defective genes are likely to be found during the next
few years, and this will make genetic testing valuable for an increasing number
of individuals who will develop colon cancer.

At present, there are two types of familial colon cancer in which defective
genes can be identified. One type of cancer is associated with a strong family
history of colon polyps. The other type of colon cancer is not associated with a
family history of colon polyps. The polyp-associated cancerous disease is called
familial adenomatous polyposis (FAP). (Adenomatous polyps are a type of polyp
that have the potential to become cancerous.) The nonpolyp-associated cancerous
disease is called hereditary nonpolyposis colorectal cancer (HNPCC).

How does someone know if he or she may be a member of a family with FAP and
may need genetic testing?

An individual is likely to belong to a family with FAP if he or she has more
than 100 adenomatous colon polyps or is a first-degree relative (parent,
sibling, or child) of a person who has more than 100 adenomatous colon polyps.
The number of polyps is less in some families, a condition referred to as
attenuated FAP. Therefore, individuals who have between 20 and 100 adenomatous
colon polyps or are first-degree relatives of individuals with 20 to100
adenomatous colon polyps also may belong to a family with FAP.

How does someone know if he or she may be a member of a family with HNPCC and
may need genetic testing?

An individual is likely to belong to a family with HNPCC and require genetic
testing if:

  1. three or more relatives have had colon cancer (or another cancer
    associated with HNPCC such as uterine, small bowel, urethral, or renal pelvic
    cancer) and at least one of the relatives is a first-degree relative,
  2. two or
    more generations of the family have colon cancer, or
  3. one or more relatives
    were diagnosed with colon cancer before age 50.

These criteria for identifying HNPCC are referred to as the Amsterdam II Criteria. The Amsterdam II Criteria
have been modified in order to identify additional individuals who should
undergo genetic testing for HNPCC. These include people with:

  1. two or more
    colon cancers,
  2. with colon cancer and a first-degree relative with colon
    cancer or another cancer associated with HNPCC before age 50, or an adenomatous colon polyp/a> before the age of 40,
  3. colon or uterine cancer before age 50, and
  4. an adenomatous colon polyp before age 50. The expanded Amsterdam II Criteria
    are referred to as the modified Bethesda Criteria.

How is genetic testing done in families suspected of being FAP families?/h3>

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