idw – Informationsdienst Wissenschaft

Nachrichten, Termine, Experten

Grafik: idw-Logo
Grafik: idw-Logo

idw - Informationsdienst

Science Video Project

idw-News App:


Google Play Store

27.11.2019 12:34

Exploring drug repurposing to treat glioblastoma

Dr. Tilmann Kiessling EMBO Communications
EMBO - excellence in life sciences

    MALT1 blockers have long been in clinical use for the treatment of blood cancers. A study suggests that these drugs could potentially also be developed as a treatment option for glioblastoma, the most common and lethal type of brain tumour.

    Heidelberg, 27 November 2019 – For a long time, cancer research has largely focused on so-called oncogenes – genes that can cause cancer when mutated. While targeting these genes has led to the successful development of a number of valuable drugs, this approach is hampered by the fact that tumours often become resistant to these treatments.

    A study conducted by Julie Gavard at the Université de Nantes, CNRS, INSERM, France, and her team, published today in The EMBO Journal, is now based on a different concept, termed non-oncogene addiction. During disease progression, cancer cells become strongly dependent on normal genes and cell functions to survive. These genes could thus serve as potential targets to attack tumour growth more efficiently. A gene called mucosa-associated lymphoid tissue l (MALT1), for example, is highly active in lymphoma, a type of blood cancer, and blocking MALT1 causes lymphoma cells to die. MALT1 blockers have been viewed as a promising new treatment for lymphomas.

    The researchers now addressed the role of MALT1 in solid tumours, namely glioblastoma. Using data from The Cancer Genome Atlas, a molecular characterization of over 20,000 primary cancers, they revealed that MALT1 levels strongly correlate with patients’ survival in brain cancer – patients with less MALT1 tend to live longer.

    Gavard and colleagues then focused their attention on so-called glioblastoma stem cells, a self-renewing subpopulation of cells within the tumour that are likely responsible for cancer recurrence after treatment. They uncovered that targeting MALT1 with MALT1 blockers caused glioblastoma stem cells to undergo a rare form of cellular suicide termed lysosomal cell death in human cell culture experiments. Lysosomes are organelles within the cell that serve as the cells’ digestive system. MALT1 keeps lysosomes low in cancer cells, which is crucial for their survival. Blocking MALT1 leads to an increase in lysosomes, which in turn impairs the cells’ waste disposal system, eventually killing them. This points to the possibility of further exploring MALT1 inhibitors as potential treatment of glioblastoma.


    Control of the Homeostasis of Endo-lysosomes by the Paracaspase MALT1 regulates Glioma Cell Survival

    The EMBO Journal

    Kathryn A. Jacobs, Gwennan André-Grégoire, Clément Maghe, An Thys, Ying Li, Elizabeth Harford-Wright1, Kilian Trillet, Tiphaine Douanne, Carolina Alves Nicolau, Jean-Sébastien Frénel, Nicolas Bidère, and Julie Gavard

    DOI: 10.15252/embj.2019102030

    Weitere Informationen:

    http://Read the paper:


    Merkmale dieser Pressemitteilung:



    Die Suche / Erweiterte Suche im idw-Archiv

    Sie können Suchbegriffe mit und, oder und / oder nicht verknüpfen, z. B. Philo nicht logie.


    Verknüpfungen können Sie mit Klammern voneinander trennen, z. B. (Philo nicht logie) oder (Psycho und logie).


    Zusammenhängende Worte werden als Wortgruppe gesucht, wenn Sie sie in Anführungsstriche setzen, z. B. „Bundesrepublik Deutschland“.


    Die Erweiterte Suche können Sie auch nutzen, ohne Suchbegriffe einzugeben. Sie orientiert sich dann an den Kriterien, die Sie ausgewählt haben (z. B. nach dem Land oder dem Sachgebiet).

    Haben Sie in einer Kategorie kein Kriterium ausgewählt, wird die gesamte Kategorie durchsucht (z.B. alle Sachgebiete oder alle Länder).