This page was reviewed under our medical and editorial policy by
Eric Fowler, MS, LCGC, Manager, Clinical Genetics, Western Region & Licensed Certified Genetic Counselor
This page was reviewed on August 11, 2021.
Inside the DNA of every cell in your body, there are genes—around 30,000 of them. They’re located on all 23 pairs of your chromosomes. You get one set of chromosomes from each parent, and together they determine all your physical characteristics.
However, a gene may change, or mutate itself. This isn’t necessarily a bad thing, because gene mutations may either lead to nothing or be beneficial. These beneficial mutations may even prevent you from getting certain disorders. For example, some people have a genetic mutation that prevents diabetes from developing.
Even when a gene mutation might cause problems, the body has a remarkable ability to correct these mutations before that problem happens.
But unfortunately, some mutations may be a possible cause of a person developing cancer in their lifetime. In fact, this is the way that all cancers start in the body—a result of multiple mutations that occur throughout someone’s life. Cancer doesn’t usually happen from a single mutation alone.
These changes in the gene, or mutations, are what cause a normal protein to become abnormal. Sometimes a mutation may prevent a protein from being created in the first place. When that protein isn’t working like it’s supposed to, it may result in additional DNA damage not being repaired and cause cells to start growing and dividing quickly and out of control. This is when cancer cells form in certain areas of the body.
There are two classes of genes that are tied to cancer: oncogenes and tumor suppressor genes.
So what are they, and how do they cause cancer?
It’s helpful to understand first that an oncogene is actually the name of a mutated proto-oncogene. Proto-oncogenes are normal genes in your body that help control cells dividing, growing, and even the rate at which they die off. This balance is what keeps your body healthy and working as it should.
But if there are too many copies of this gene, or it mutates, it may become hyperactivated, which means cell growth and division get out of control. Cancer cells start to form from what used to be normal cells. Once a mutation occurs, the proto-oncogene is referred to as an oncogene.
Usually, these mutations aren’t inherited, which means they aren’t passed from a parent to a child. They, like most cancers, are acquired, meaning they happen because of damage to genes. These mutations are only present in certain cells, not every cell in the body, as is the case with inherited mutations.
Oncogenes (former proto-oncogenes) are activated and cause cells to grow and divide too quickly because of a mutation. Tumor suppressor genes, on the other hand, work slightly differently.
Tumor suppressor genes are normal genes located inside cells. Their job is to regulate cell growth and division and repair acquired DNA damage. They keep cells from growing too fast, but when mutations occur, the gene becomes inactivated or shut itself off. This causes cells to start growing out of control because the gene no longer has the ability to limit its growth and how quickly the cell divides. The result is the same as that which occurs with oncogenes—cell growth that happens too quickly and out of control, leading to the development of cancer cells.
Most of the time, like oncogenes, these mutations aren’t inherited, but acquired, meaning they happen after you’ve been born.