
Cancer has many possible causes, but sometimes it can be linked to changes in your genes, called gene mutations. Since genetic codes are inherited, the same mutation is often found among different family members. If you have a number of relatives with breast or ovarian cancer, a BRCA gene mutation could run in your family.
“Everyone has the BRCA1 and BRCA2 genes, but having a mutation on those gene lines increases your risk for breast and ovarian cancer,” says Darshna Chandrasekhara, MD, an OBGYN in Irving, Texas.
More than 60 percent of women with either mutation will develop breast cancer at some point, according to the National Cancer Institute (NCI). Women with a BRCA1 mutation also have a 39 to 58 percent lifetime risk of developing ovarian cancer, while women with a BRCA2 mutation have a 13 to 29 percent risk.
“Those numbers are shocking, but only 5 to 10 percent of people with breast cancer actually have the genetic type. That means people should only get tested if they’re truly at risk for the mutation,” explains Dr. Chandrasekhara.
What are the BRCA genes?
Normally, the BRCA genes help prevent cancer. Cancer happens when a group of cells start growing too much or too quickly, but the BRCA genes keep your breast and ovarian cells from growing out of control.
If you have a BRCA gene mutation, you’re less protected, but you won’t necessarily develop cancer. That’s because you have two copies of each gene—one from your mother and one from your father. If there’s a mutation on one copy of a gene, the other one may still work.
However, if the working copy gets damaged, cancer could develop. Things that can harm a gene include:
- Tobacco
- Alcohol
- Exposure to radiation or certain chemicals
A poor diet and lack of exercise may also cause damage. In fact, nearly 1 in 5 cancers in the United States have been linked to preventable causes like these.
Should I get tested for BRCA gene mutations?
Your healthcare provider (HCP) may recommend genetic testing if you have:
- A close relative with the BRCA1 or BRCA2 mutation
- A personal history of breast cancer at age 45 or younger, or of ovarian, tubal, or peritoneal cancer at any point
- A family history of breast cancer at age 50 or younger, or of ovarian cancer, pancreatic cancer, high-risk prostate cancer, or male breast cancer at any point
- Eastern or Central European (Ashkenazi) Jewish ancestry
“There are two ways to test for mutations," says Chandrasekhara. "You can have a blood test, or you can have your cheek cells tested. For the cheek test, you’ll swish around mouthwash and then spit it into a cup,” she explains. After that, a lab will filter out your cheek cells and break them down to complete the genetic testing.
What to do if you test positive
If you learn you’re a mutation carrier, work with your OBGYN to decide how often you’ll need to complete screenings for breast cancer, such as:
- Clinical breast exams. These are typically done twice a year starting around age 25.
- Magnetic resonance imaging (MRI). “Annual breast MRIs are recommended between ages 25 to 29 because mammograms aren’t usually helpful in younger people,” says Chandrasekhara. “Younger breasts can be very dense, so mammograms aren’t able to pick up on changes as easily.”
- Mammograms. An annual mammogram and breast MRI are both recommended starting at age 30, according to the NCI.
There are screening tests available for ovarian cancer as well, but these tests aren’t always reliable. You and your HCP should discuss whether ovarian cancer screening is right for you.
How to lower your cancer risk
Along with a careful screening schedule, you can lower your risk by:
- Breastfeeding. “Twelve months of cumulative breastfeeding—even if it’s from different pregnancies—adds up to lower your risk of breast cancer,” says Chandrasekhara. Plus, pregnancy in general may lower your risk of ovarian cancer.
- Maintaining a healthy weight. A body mass index (BMI) of 25 or higher raises cancer risk.
- Avoiding alcohol and tobacco. Find an addiction specialist near you or make a plan to quit tobacco.
Some people undergo preventive chemotherapy or operations to keep cancer from developing. For example, a bilateral mastectomy, during which both breasts are removed, reduces your breast cancer risk by 90 percent, says Chandrasekhara. To reduce the risk of ovarian cancer, others choose to have a risk-reducing salpingo-oophorectomy (RRSO), a procedure during which the ovaries and fallopian tubes are removed. The choice to have preventive chemotherapy or surgery should be based on your age, mutation type, and desire to start a family.
If you have a strong family history of breast or ovarian cancer, ask your HCP if you’re a candidate for genetic testing at your next appointment.
Sources: American College of Obstetricians and Gy... + 16
- American College of Obstetricians and Gynecologists. BRCA1 and BRCA2 Mutations. April 2025.
- National Cancer Institute. BRCA Gene Changes: Cancer Risk and Genetic Testing. July 19, 2024.
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