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Chronic Myeloid Leukemia (CML)
- Targeted Therapy Drugs for Chronic Myeloid Leukemia
- Interferon Therapy for Chronic Myeloid Leukemia
- Chemotherapy for Chronic Myeloid Leukemia
- Radiation Therapy for Chronic Myeloid Leukemia
- Surgery for Chronic Myeloid Leukemia
- Stem Cell Transplant for Chronic Myeloid Leukemia
- How Do You Know If Treatment for Chronic Myeloid Leukemia Is Working?
- Treating Chronic Myeloid Leukemia by Phase
- References: Chronic Myeloid Leukemia
- If You Have Chronic Myeloid Leukemia (CML)
What Causes Chronic Myeloid Leukemia?
Normal human cells grow and function based mainly on the information contained in each cell's chromosomes. Chromosomes are long molecules of DNA in each cell. DNA is the chemical that carries our genes, the instructions for how our cells function. We look like our parents because they are the source of our DNA. But our genes affect more than the way we look.
Each time a cell prepares to divide into 2 new cells, it must make a new copy of the DNA in its chromosomes. This process is not perfect, and errors can occur that may affect genes within the DNA.
Some genes control when our cells grow and divide.
- Certain genes that promote cell growth and division are called oncogenes.
- Others that slow down cell division or cause cells to die at the right time are calledtumor suppressor genes.
Cancers can be caused by changes in DNA (mutations) that turn on oncogenes or turn off tumor suppressor genes.
Over the past few years, scientists have made great progress in understanding how certain changes in DNA can cause normal bone marrow cells to become leukemia cells. In no cancer is this better understood than in chronic myeloid leukemia (CML).
Each human cell contains 23 pairs of chromosomes. Most cases of CML start during cell division, when DNA is "swapped" between chromosomes 9 and 22. Part of chromosome 9 goes to 22 and part of 22 goes to 9.
This is known as a translocation and it makes a chromosome 22 that's shorter than normal. This new abnormal chromosome is called the Philadelphia chromosome.The Philadelphia chromosome is found in the leukemia cells of almost all patients with CML
The swapping of DNA between the chromosomes leads to the formation of a new gene (an oncogene) called BCR-ABL. This gene then produces the BCR-ABL protein, which is the type of protein called a tyrosine kinase. This protein causes CML cells to grow and divide out of control.
In a very small number of CML patients, the leukemia cells have the BCR-ABL oncogene but not the Philadelphia chromosome. It's thought that the BCR-ABL gene must form in a different way in these people. In an even smaller number of people who seem to have CML, neither the Philadelphia chromosome nor the BCR-ABL oncogene can be found. They might have other, unknown oncogenes causing their disease and are not considered to truly have CML.
Sometimes people inherit DNA mutations from a parent that greatly increase their risk of getting certain types of cancer. But mutations passed on by parents do not cause CML. DNA changes related to CML occur during the person's lifetime, rather than having been inherited before birth.
The American Cancer Society medical and editorial content team
Our team is made up of doctors and oncology certified nurses with deep knowledge of cancer care as well as editors and translators with extensive experience in medical writing.
American Society of Clinical Oncology. Leukemia - Chronic Myeloid - CML: Treatment Options. 11/2016. Accessed at www.cancer.net/cancer-types/leukemia-chronic-myeloid-cml/introduction on May 14, 2018.
National Cancer Institute. Chronic Myelogenous Leukemia Treatment (PDQ)-Patient Version. March 30, 2018. Accessed at www.cancer.gov/types/leukemia/patient/cml-treatment-pdq on May 14, 2018.
Last Revised: June 19, 2018
American Cancer Society medical information is copyrighted material. For reprint requests, please see our Content Usage Policy.
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