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Blood cancer cells initiate signalling cascade

Date:
August 13, 2012
Source:
Albert-Ludwigs-Universität Freiburg
Summary:
Scientists have uncovered how pathological cells activate themselves in chronic lymphocytic leukemia. They have identified a new mechanism that causes immune cells to convert into malignant cancer cells. In chronic lymphocytic leukemia, one of the most common types of blood cancer in the Western world, cells themselves carry the key for the pathogenic transformation, the scientists report.

In patients with Chronic Lymphocytic Leukaemia, two receptors dock at the outside of white blood cells (top, in blue) and use receptor components at the inside of the cell (bottom) to trigger a signalling cascade. This in turn is an important step of the conversion into an uncontrolled dividing cancer cell.
Credit: Dühren-von Minden

Freiburg scientists have uncovered how pathological cells activate themselves in chronic lymphocytic leukemia.

Researchers in the group of Prof. Dr. Hassan Jumaa, Centre for Biological Signalling Studies (BIOSS) of the University of Freiburg, Department for Molecular Immunology, have identified a new mechanism that causes immune cells to convert into malignant cancer cells. In Chronic Lymphocytic Leukemia (CLL), one of the most common types of blood cancer in the Western world, cells themselves carry the key for the pathogenic transformation, the scientists report in the journal “Nature”. Understanding these underlying mechanisms could facilitate new therapies with reduced side effects.

In healthy humans, a subgroup of white blood cells, so-called B-lymphocytes, are responsible for producing antibodies that fight infections. Special receptor molecules of B-lymphocytes detect pathogenic agents via the key-lock principle and consequently start producing antibodies. In patients with CLL, however, abnormal forms of these receptors lead to uncontrolled reproduction of malignant B-lymphocytes. As a result, healthy cells of the immune system get repressed.

“Up to now, it was assumed that agents produced in the bodies of patients dock at the receptor and thereby activate CLL lymphocytes”, Jumaa says. “In our study we could show that specific components of the receptors are responsible for the development of CLL.” In B-lymphocytes of CLL patients, receptor components FR2 and HCDR3 are formed in such a manner that they represent key and lock of the receptor. “Hereby, neighboring receptors of the same cells activate each other and trigger a signalling cascade, which finally causes uncontrolled division of cancer cells.”

Currently, approaches like chemotherapy that suppress symptoms in a relatively unspecific manner are applied in CLL treatment. “Based on decoding the molecular basics of CLL, we now strive to translate this knowledge to make it useful for patients”, Marcus Dühren-von Minden says, another author of the study. “It is conceivable to administer numerous copies of the key FR2 to patients, which then dock to the receptors and prevent neighboring receptors to bind at each other. This stops the consequential signalling cascade.” Through this mechanism, the course of the disease could be precluded much earlier than before, and with less side effects.

The research team is a member of the Cluster of Excellence BIOSS of the Albert-Ludwigs-University of Freiburg. The project is a collaboration between researchers from the University of Freiburg, the Max Planck Institute of Immunobiology Freiburg, and the University Hospital of Freiburg. It strives at to gain insights about the development of CLL and is funded by the Deutsche Krebshilfe (German Cancer Aid) and the Deutsche Forschungsgemeinschaft (German Research Foundation).


Story Source:

The above story is based on materials provided by Albert-Ludwigs-Universität Freiburg. Note: Materials may be edited for content and length.


Journal Reference:

  1. Marcus Dühren-von Minden, Rudolf Übelhart, Dunja Schneider, Thomas Wossning, Martina P. Bach, Maike Buchner, Daniel Hofmann, Elena Surova, Marie Follo, Fabian Köhler, Hedda Wardemann, Katja Zirlik, Hendrik Veelken, Hassan Jumaa. Chronic lymphocytic leukaemia is driven by antigen-independent cell-autonomous signalling. Nature, 2012; DOI: 10.1038/nature11309

Cite This Page:

Albert-Ludwigs-Universität Freiburg. "Blood cancer cells initiate signalling cascade." ScienceDaily. ScienceDaily, 13 August 2012. <www.sciencedaily.com/releases/2012/08/120813074019.htm>.
Albert-Ludwigs-Universität Freiburg. (2012, August 13). Blood cancer cells initiate signalling cascade. ScienceDaily. Retrieved September 23, 2014 from www.sciencedaily.com/releases/2012/08/120813074019.htm
Albert-Ludwigs-Universität Freiburg. "Blood cancer cells initiate signalling cascade." ScienceDaily. www.sciencedaily.com/releases/2012/08/120813074019.htm (accessed September 23, 2014).

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