Blocking the Migration of Cancer Cells to Destroy Them
News Aug 09, 2016
Lymphoma is a cancer that affects lymphocytes, a type of white blood cell. The disease originates in a lymphoid organ (lymph node, spleen, or bone marrow) before spreading through the blood to infiltrate not only other lymphoid organs but also other tissues. Every year, nearly 2,000 people in Switzerland are diagnosed with lymphoma, a disease that can be very aggressive, resisting standard treatments with chemotherapeutic drugs. Today, researchers at the University of Geneva (UNIGE) and the Geneva University Hospitals (HUG), Switerland, give a new hope to patients. Their innovative approach consists in using an antibody able to neutralize a specific protein to block the migration of lymphoma cells, thus preventing the disease from developing. This still experimental immunotherapeutic strategy paves the way for new treatments against lymphoma. The results can be read in the Journal of Leukocyte Biology.
Lymphocytes, a special type of white blood cell, are essential components of the immune system. But like any other cell, they are not safe from carcinogenic mutations that can cause uncontrolled proliferation. They can then circulate freely in the blood and spread to the lymphatic system, thus causing a tumor called lymphoma.
Lymphoma cells only become truly dangerous when they leave the blood vessels and multiply in the lymphatic system. ‘Since they cannot survive in the blood for long, these malignant cells are compelled to find a more accommodating environment – such as the lymphatic system – where they can proliferate. We decided to focus on this Achilles heel by containing them in the blood so as to prevent any resulting harm’, explains Thomas Matthes, Professor at UNIGE, Faculty of Medicine, and Doctor at HUG, who supervised the study together with Beat Imhof, Professor at UNIGE, Faculty of Medicine.
A way to prevent malignant cell circulation
The inner wall of blood vessels is formed by a layer of endothelial cells that act as a barrier, which prevents the blood cells from leaving the circulation. Yet, some lymphocytes, having mutated to become cancerous, are equipped with a specific surface marPRESS RELEASE Geneva | 4 August 2016 Blocking the migration of cancer cells to destroy them Scientists in Geneva developed an antibody able to fight off lymphomas Blocking JAM-C on lymphoma cells inhibits their migration through vessel walls.
A two-faceted antibody
The H225 antibody proved itself very efficient, decreasing the transit of cancerous cells into the organs of the lymphatic system by over 50%. ‘This is not its only effect, Thomas Matthes adds, H225 also significantly limited cell proliferation, even when tumor cells had already settled in the lymphatic system. In our mice, we observed the nearly-complete disappearance of already-present tumor cells in the organs.’
This discovery is in line with the recent advances in cancer immunotherapy, a field that focuses on the design of treatments based on the human immune system. With their specific interest in the JAM-C marker, the Geneva team has laid the foundation for a new therapeutic strategy against lymphoma. The researchers now focus their ongoing efforts on the quest for an efficient treatment that could, in the near future, be offered to patients.
Human Malaria Parasites Grown for the First Time in Dormant FormNews
One of the biggest obstacles to eradicating malaria is a dormant form of the parasite which is resistant to most antimalarial drugs and can reawaken years later, causing disease relapse. Researchers have shown they can grow the dormant parasite in engineered human liver tissue for several weeks, allowing them to closely study how the parasite becomes dormant, what vulnerabilities it may have, and how it springs back to life.READ MORE
Gut Bacteria Latest Ally in Fight Against SepsisNews
Sepsis occurs when the body's response to the spread of bacteria or toxins to the bloodstream damages tissues and organs. The fight against sepsis could get a helping hand from a surprising source: gut bacteria. Researchers found that giving mice particular microbes increased blood levels of immunoglobulin A (IgA) antibodies, which protected against the kind of widespread bacterial invasion that leads to sepsis.READ MORE