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Researchers have found several factors that can increase a person’s risk of colorectal cancer, but it’s not yet clear exactly how all of these factors might cause this cancer.
Cancer is caused by changes in the DNA inside our cells. DNA is the chemical in our cells that makes up our genes, which control how our cells function. We usually look like our parents because they are the source of our DNA. But DNA affects more than just how we look.
Some genes help control when our cells grow, divide into new cells, and die:
Cancers can be caused by DNA mutations (changes) that turn on oncogenes or turn off tumor suppressor genes. This leads to cells growing out of control. Changes in many different genes are usually needed to cause colorectal cancer.
For more about how genes changes can lead to cancer, see Genes and Cancer.
Some DNA mutations can be passed on in families and are found in all of a person's cells. These are called inherited mutations. A very small portion of colorectal cancers are caused by inherited gene mutations. Many of these DNA changes and their effects on the growth of cells are now known. For example:
Special genetic tests can find gene mutations linked to these inherited conditions. If you have a family history of colorectal polyps or cancer or other symptoms linked to one of these conditions, you may want to ask your doctor about genetic counseling and genetic testing.
The American Cancer Society recommends discussing genetic testing with a qualified cancer genetics professional before any genetic testing is done. For more on this, see Understanding Genetic Testing for Cancer Risk and What Happens during Genetic Testing for Cancer Risk?
Most gene mutations that lead to cancer are acquired mutations. They happen during a person’s lifetime and are not passed on to their children. These DNA changes affect only cells that come from the original mutated cell.
In most cases of colorectal cancer, the DNA mutations that lead to cancer are acquired during a person’s life rather than having been inherited. Certain risk factors probably play a role in causing these acquired mutations, but so far it’s not known what causes most of them.
There doesn’t seem to be a single genetic pathway to colorectal cancer that's the same in all cases. In many cases, the first mutation occurs in the APC gene. This leads to an increased growth of colorectal cells because of the loss of this “brake” on cell growth. Further mutations may then occur in other genes, which can lead the cells to grow and spread uncontrollably. Other genes that aren’t known yet are probably involved as well.
Our team is made up of doctors and oncology certified nurses with deep knowledge of cancer care as well as journalists, editors, and translators with extensive experience in medical writing.
Lawler M, Johnston B, Van Schaeybroeck S, Salto-Tellez M, Wilson R, Dunlop M, and Johnston PG. Chapter 74 – Colorectal Cancer. In: Niederhuber JE, Armitage JO, Dorshow JH, Kastan MB, Tepper JE, eds. Abeloff’s Clinical Oncology. 6th ed. Philadelphia, Pa. Elsevier: 2020.
Libutti SK, Saltz LB, Willett CG, and Levine RA. Ch 62 - Cancer of the Colon. In: DeVita VT, Hellman S, Rosenberg SA, eds. DeVita, Hellman, and Rosenberg’s Cancer: Principles and Practice of Oncology. 11th ed. Philadelphia, Pa: Lippincott-Williams & Wilkins; 2019.
Maisonneuve P, Lowenfels AB. Cancer in cystic fibrosis: A narrative review of prevalence, risk factors, screening, and treatment challenges: Adult Cystic Fibrosis Series. Chest. 2022;161(2):356-364.
National Cancer Institute. Genetics of Colorectal Cancer (PDQ®)–Health Professional Version. https://www.cancer.gov/types/colorectal/hp/colorectal-genetics-pdq#link/_2606. Updated January 27, 2020. Accessed February 7, 2020.
Last Revised: July 19, 2023
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