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What Causes Acute Myeloid Leukemia (AML)?

Some people with acute myeloid leukemia (AML) have one or more known risk factors. But it can be very hard to know if any of these factors actually caused the cancer.

Changes (mutations) in genes as a cause of AML

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. Our DNA, which comes from both our parents, affects more than just how we look.

Some genes normally help control when our cells grow, divide to make new cells, or repair mistakes in DNA, or they cause cells to die when they’re supposed to. If these genes aren’t working properly, it can lead to cells growing out of control. For example:

  • Changes in genes that normally help cells grow, divide, or stay alive can lead to these genes being more active than they should be, causing them to become oncogenes. These genes can result in cells growing out of control.
  • Genes that normally help keep cell division under control or cause cells to die at the right time are known as tumor suppressor genes. Changes that turn off these genes can result in cells growing out of control.
  • Some genes normally help repair mistakes in a cell’s DNA. Changes that turn off these DNA repair genes can result in the buildup of DNA changes within a cell, which might lead to them growing out of control.

Any of these types of DNA changes might lead to cells growing out of control, which might lead to cancer, including AML. For instance, changes in certain genes such as FLT3, c-KIT, and RAS are common in AML cells. These types of changes can stop bone marrow cells from maturing the way they normally would, or help the cells grow out of control.

To learn more, see Oncogenes, Tumor Suppressor Genes, and DNA Repair Genes.

Chromosome changes in AML cells

The DNA inside each cell is in long strands called chromosomes. Each time a cell divides into 2 new cells, it must make a new copy of its chromosomes. This process isn't perfect, and errors can occur that affect genes within the chromosomes.

Mutations in many different genes can be found in AML cells, but larger changes in one or more chromosomes are also common. Even though these changes involve larger pieces of DNA, their effects are still likely to be due to changes in just one or a few genes that are on that part of the chromosome. Several types of chromosome changes might be found in AML cells:

  • Translocations are the most common type of chromosome change. A translocation means that a part of one chromosome breaks off and becomes attached to a different chromosome. The point at which the break occurs can affect nearby genes – for example, it can turn on oncogenes or turn off genes like RUNX1 and RARa, which would normally help blood cells to mature.
  • Deletions occur when part of a chromosome is lost. This can result in the cell losing a gene that helped keep its growth in check (a tumor suppressor gene).
  • Inversions occur when part of a chromosome gets turned around, so it’s now in reverse order. This can result in the loss of a gene (or genes) because the cell can no longer read its instructions (much like trying to read a book backward).
  • Addition or duplication means that there is an extra chromosome or part of a chromosome. This can lead to too many copies of certain genes within the cell. This can be a problem if one or more of these genes are oncogenes.

There are many types of AML, and different types can have different gene and chromosome changes, some of which are more common than others. Doctors are trying to figure out why these changes occur and how each of them might lead to leukemia. For example, some are more common in AML that occurs after chemotherapy for another cancer.

Some changes seem to have more of an effect on a person’s prognosis (outlook) than others. For instance, some changes might affect how quickly the leukemia cells grow, or how likely they are to respond to treatment. This is discussed in more detail in Acute Myeloid Leukemia (AML) Subtypes and Prognostic Factors.

Inherited versus acquired gene changes in AML

Some people with certain types of cancer inherit gene mutations from a parent that increase their risk for the disease. Although this can happen sometimes with AML, such as with the genetic syndromes discussed in Risk Factors for Acute Myeloid Leukemia (AML), inherited mutations are not a common cause of AML.

Most DNA changes related to AML are acquired during a person’s lifetime, rather than having been inherited before birth. Some of these changes may have outside causes like radiation or cancer-causing chemicals, but most often the reason they occur isn't clear. Many of these gene changes are probably just random events that sometimes happen inside a cell, without having an outside cause. They seem to happen more often as we age, which might help explain why AML usually occurs in older people.

 

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Developed by the American Cancer Society medical and editorial content team with medical review and contribution by the American Society of Clinical Oncology (ASCO).

Appelbaum FR. Chapter 95: Acute Leukemias in Adults. In: Niederhuber JE, Armitage JO, Doroshow JH, Kastan MB, Tepper JE, eds. Abeloff’s Clinical Oncology. 6th ed. Philadelphia, Pa: Elsevier; 2020.

National Cancer Institute. Acute Myeloid Leukemia Treatment (PDQ®)–Health Professional Version. 2024. Accessed at https://www.cancer.gov/types/leukemia/hp/adult-aml-treatment-pdq on November 25, 2024.

Stock W, Thirman MJ. Acute myeloid leukemia: Pathogenesis. UpToDate. 2024. Accessed at https://www.uptodate.com/contents/acute-myeloid-leukemia-pathogenesis on November 25, 2024.

 

Last Revised: March 4, 2025

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