Genetic Testing
Cancer Care Centers of South Texas offers genetic testing for individuals who may be at hereditary risk for certain types of cancers. Genetic testing involves analyzing the DNA for a genetic alteration, or mutation, that may indicate an increased risk for developing a specific type of cancer. Genetic counseling is helpful in assessing an individual's hereditary risk factors to aid in determining if genetic testing is necessary or of value. This involves a communication process between a specially-trained health professional and the person or family concerned about their genetic risk for cancer, and includes discussion of the person's and/or family's medical history.
Cancer Care Centers of South Texas offers genetic testing for the following hereditary risk factors:
- Assessment of a woman's risk for developing breast or ovarian cancer. Genetic testing is based on the detection of mutations in the BRCA1 and BRCA2 genes.
- Assessment of the hereditary risk of developing hereditary colorectal and endometrial cancer (hereditary nonpolyposis colorectal cancer, or HNPCC). This test is based on the detection of mutations in three genes, MLH1, MSH2, and MSH6.
- Assessment of the risk of hereditary colorectal polyps and cancer. Testing involves the detection of mutations in the APC and MYH genes, which cause adenomatous polyposis syndromes which includes familial adenomatous polyposis (FAP), attenuated FAP (AFAP), and MYH-associated polyposis (MAP).
- Assessment of the inherited susceptibility to melanoma and pancreatic cancer. Testing is based on the detection of inherited mutations in the p16 gene. These mutations occur in approximately 40% of families with hereditary melanoma.
Are you at risk?
Family members will benefit from this information, as well as you, since hereditary cancer risk can be significantly reduced by the right medical interventions. A careful review of your family history is an essential first step. To carefully review your family history, please the questions below that apply to you:
Your personal cancer diagnosis _______________________________.
Have YOU been diagnosed with......(answer with yes, no, or uncertain)
Breast cancer before the age of 50?
Ovarian cancer at any age?
Two breast cancers, or breast and ovarian cancer?
Male breast cancer at any age?
Colon or uterine cancer before age 50?
Colon or uterine cancer at any age with a family history of either?
Two colon cancers, or colon and uterine cancer?
10 or more colon polyps (lifetime)?
Two or more melanomas?
Melanoma and pancreatic cancer?
Are you of Ashkenazi (Central or Eastern European) Jewish ancestry?
Have any of your FAMILY members (blood relatives such as parents, grandparents, brothers, sisters, aunts, uncles, nieces or nephews) been diagnosed with......
Breast cancer before age 50?
Ovarian cancer at any age?
Two breast cancers, or breast and ovarian?*
Male breast cancer at any age?
Colon or uterine cancer before age 50?
Colon or uterine cancer at any age with a family history of either?
Two colon cancers, or colon and uterine cancer?
10 or more colon polyps (lifetime)?
Two or more melanomas?
Melanoma and pancreatic cancer?
Are you of Ashkenazi (Central or Eastern European) Jewish ancestry?
*Can be two cancers in one person, or two or more people in your family with these cancers.
If you answered YES to any of these questions, you may have an inherited risk for developing cancer. Please call one of our locations for an appointment to learn more about genetic counseling and genetic testing.





