
Cancer is a general term for the abnormal growth of cells in the body. There are millions of cells in the body, and each cell contains DNA (the genetic blueprint for life). DNA provides millions of messages to the genes, which tell the body how to grow, function and behave. Sometimes there is a mistake in one of the messages, called a mutation. Cancer results when a gene sends the wrong message to a cell and the cell multiplies repeatedly. As the cancer cells grow it may be felt in the form of a solid mass or bump or lump. The words tumor, mass, nodule, or lump are all used to refer to a collection of cells. A mass can be benign (no cancer) or malignant (cancer) but only a biopsy or sampling of the cells can determine a cancer diagnosis.
Each year, 78,000 women in the United States learn they have a gynecologic cancer. Although these cancers are often grouped together, they vary widely in their causes, risk factors, detection, treatment and chance of a cure. For more information about breast and gynecologic cancers, click on the links below.
Although most cancers are not hereditary, some cases do involve an inherited risk for a specific cancer. Everyone has BRCA1 and BRCA2 genes, which normally help to prevent cancer by telling DNA to instruct cells not to grow abnormally. However, some individuals inherit a mutation in one of these genes, possibly resulting in the DNA allowing cells to grow abnormally.
Working in collaboration with the GenRISK® Adult Genetics Program at Cedars-Sinai, the Women's Cancer Research Institute can help patients determine their genetic risk for cancer. For more information, click the links* below.
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