Here's How Stress Hormone Prevents Blood Cancer
Malignant AML cells then use cortisol to increase the release of latrophilin 1 so that they can use it to avoid the immune system.
Washington D.C., Aug 15: A human stress hormone called cortisol has been identified by scientists as a key factor behind when and why the immune system fails to prevent leukemia from taking hold. The team led by Dr. Vadim Sumbayev, of the University's Medway School of Pharmacy, found for the first time that blood or bone marrow cancer - acute myeloid leukemia (AML) - cells evade the anti-cancer activity of the human immune system by employing the human hormone cortisol. The study of the causes of AML - the most severe blood or bone marrow cancer, demonstrated that AML cells employ a unique pathway for the disease to progress, using functional systems of the human body to both support their survival and also reduce the anticancer activities of immune cells.
They do this by using cortisol to force the release of a protein, latrophilin 1. This, in turn, causes the secretion of another protein, galectin-9, which suppresses the body's natural anti-cancer immune mechanism. Dr. Sumbayev's team, working with researchers from two German universities and the UK's Diamond Light Source facility, found that although healthy human white blood cells are not affected by cortisol, they become capable of releasing latrophilin 1 when the malignant transformation takes place. Malignant AML cells then use cortisol to increase the release of latrophilin 1 so that they can use it to avoid the immune system.
Dr. Sumbayev said, "For the first time, we can identify a possible future pathway to develop an effective new therapy using the body's natural immune mechanisms. We have discovered a new fundamental biochemical mechanism within the human body that allows AML cells to employ physiological systems to survive and escape immune attack."
The study concluded that galectin-9, as well as a natural binding partner of latrophilin 1 - known as FLRT3 - which are both present in human blood plasma, are the most promising targets for future anti-AML immune therapy.
The full findings are present in the journal- Cellular and Molecular Immunology.