Sorry, you need to download flash or use a more modern browser.
Chapter: 5 - Types & Stages
Subchapter: 6 - Triple Negative Breast Cancer
In Subchapter 3.1, “Growth of Cancer”, we discussed the role of receptors in cancer cells. Doctors seek to determine what causes certain types of cancer to progress by identifying its “receptors”. These receptors function like mouths: when open, the cancer cells feed and rapidly grow.
Triple Negative Breast Cancer tumors lack receptors for any of three bodily chemicals: estrogen, progesterone, and the HER2/neu gene. There are still effective treatments for it, such as chemotherapy, but doctors are not sure what stimulates this type of tumor to grow.
Women with a family history of breast cancer, specifically with the BRCA1 or BRCA2 breast gene mutation, are more at risk for developing Triple Negative Breast Cancer.
Introduction 01:13
Stage 0 & 1 00:53
Stage 2 01:28
Stage 3 02:26
Stage 4 01:05
Asked by anonymous
Learning About Breast Cancer
Hi Megan genetic testing for the BRCA 1 and BRCA 2 are used post surgery as a further test to determine the treatment course. A positive result tells you that you carry the breast cancer gene the doctor might want to be more aggressive with her treatment and maybe suggesting removal of her...
Hi Megan genetic testing for the BRCA 1 and BRCA 2 are used post surgery as a further test to determine the treatment course. A positive result tells you that you carry the breast cancer gene the doctor might want to be more aggressive with her treatment and maybe suggesting removal of her ovaries. A positive results will also help the family members male and female siblings and children get better monitoring and screening like earlier mammograms then age 50 or blood test and ultra sounds to screen for ovarian, prostrate and testicular cancers A negative results says that one doesn't carry the breast cancer gene but they are only testing two genes there maybe more that they are unable to test at this time. A positive or negative result does not mean you will or will not get cancer. It is just saying the gene is or is not present.
I had the BRCA testing 2 years ago after my surgery. Now my daughter and nieces are having trouble being carried by health insurance for "per-existing condition" be sure to consult this concern with her oncologist.
Comment 0
Asked by anonymous
Learning About Breast Cancer
I am sorry about your mom's diagnosis. If you decide to get genetic testing, make sure you see a genetic counselor and/or a geneticist and ask that doctor if you are a candidate for BART testing. The genetic testing process is more complex than most people think. Your geneticist can explain the...
I am sorry about your mom's diagnosis. If you decide to get genetic testing, make sure you see a genetic counselor and/or a geneticist and ask that doctor if you are a candidate for BART testing. The genetic testing process is more complex than most people think. Your geneticist can explain the different available tests. There is "basic" testing and BART testing. My mother, who has fought breast cancer 3 times, tested BRCA negative after her first diagnosis in 2006 but she in fact really wasn't. (She only had the "basic" test). When I was diagnosed in 2010, I consulted a geneticist with enough brains to order BART genetic testing for me, which confirmed I have a BRCA2 mutation. My mother was re-tested and is also positive. Several cousins were subsequently tested and are also positive. If I hadn't had the BART test, they would not have known. Genetic testing is a scary process but it can give you and your family potentially life-saving information.
Yes. It's the BRCA 1 and BRCA 2 genetic test to see if you carry the breast cancer gene. Having the gene doesn't necessarily mean you will get breast cancer, but it may increase your chances and give you information to take care of yourself and be proactive.
Here is some information from...
Yes. It's the BRCA 1 and BRCA 2 genetic test to see if you carry the breast cancer gene. Having the gene doesn't necessarily mean you will get breast cancer, but it may increase your chances and give you information to take care of yourself and be proactive.
Here is some information from www.breastcenter.com on the test:
In 1994, the first gene associated with breast cancer — BRCA1 (for BReast CAncer1) was identified on chromosome 17. A year later, a second gene associated with breast cancer — BRCA2 — was discovered on chromosome 13. When individuals carry a mutated form of either BRCA1 or BRCA2, they have an increased risk of developing breast or ovarian cancer at some point in their lives. Children of parents with a BRCA1 or BRCA2 mutation have a 50 percent chance of inheriting the gene mutation.
Your Mom's doctor would probably be able to refer you to a genetic counselor to have the test done. They do take a sample of your spit instead of a blood test now. It's an easy test to take, but can cost quite a bit (fyi).
Hope that helps!
Good luck and all the best to your Mom!!!
Asked by anonymous
Family Member or Loved One
It can be. See if you can get the brace test to see if you or she is positive.
3 comments 0It can be Randall, but in over 75% of women diagnosed with breast cancer...there is no family history at all. I wasn't aware of this until I was diagnosed last year. I had no family history of breast cancer. I do think it's a good idea to have the genetic BRACA testing performed. If a woman...
It can be Randall, but in over 75% of women diagnosed with breast cancer...there is no family history at all. I wasn't aware of this until I was diagnosed last year. I had no family history of breast cancer. I do think it's a good idea to have the genetic BRACA testing performed. If a woman tests positive for the gene, she will need to look at more options in her treatment, and there are several more things to be considered as well in a positive result.
No related story
Looking for another topic? Use the search box in the top right.
“ An Early Detection Plan (EDP) significantly increases the chances of surviving breast cancer. ”
spread the word