The Breast Cancer Susceptibility Gene (BRCA)
is responsible for approximately 5% of breast cancer cases in America. Though
the overwhelming majority of cases diagnosed are not associated with BRCA1 or
BRCA2, the risk is still present. Before
you go to your doctor to request a BRCA genetic test, here a few things to
know.
Cancer is disease resulting from a gene
that has gotten out of control. Genes tell the cells what to do, specifically
what type of protein to create. The
Breast Cancer Susceptibility Genes (BRCA1 & BRCA2) are codes for proteins
that help to maintain the stability of DNA (deoxyribonucleic acid). BRCA1 is associated with increased risk of
breast, cervical, uterine, colon, and pancreatic cancers. BRCA2 is associated with increased risk of
ovarian, pancreatic, bile duct, gallbladder, and stomach cancers.
Men can also be affected with male
breast cancer from these genes.
Additionally, BRCA1 in men is associated with increased risk of
testicular cancer, and BRCA2 is associated with increased risk of prostate
cancer.
Not everyone needs BRCA genetic testing. Only people who have a strong family history
for breast and ovarian cancer should be tested for BRCA. If you have a sister, mother, or aunt who was
diagnosed with breast or ovarian cancer before menopause or a brother, father
or uncles who was diagnosed with breast cancer, then discuss this with your
physician. Remember an association is
not a definite diagnosis, so speak with your doctor to determine risk factors
prior to genetic testing. If you do not
know your family history, then it may be reasonable to have the BRCA test.
Routine breast self-exam and
mammography remain the best ways to screen for breast cancer. Make it your mission to regularly schedule
your annual mammogram starting at age 40 or earlier if you have a family
history; remind your sisters, friends, and family to do the same. Though Breast Cancer Awareness Month isn’t
until October, health awareness is necessary year round and can be the
difference between life and death.
Be well.
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