Characterization of the Menin-MLL Interaction as Therapeutic Cancer Target
Autor: | Andrea Haegebarth, Stephan Siegel, Bernard Haendler, Uwe Eberspaecher, Antonius Ter Laak, Nicolas Werbeck, Ralf Lesche, Carlo Stresemann, Amaury Ernesto Fernandez-Montalvan, Ursula Moenning, Krzysztof Brzezinka, Ashley Eheim, Ekaterina Nevedomskaya |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Cancer Research Biology lcsh:RC254-282 Article 03 medical and health sciences 0302 clinical medicine In vivo Prostate hemic and lymphatic diseases medicine cancer chemical probe Cancer lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens medicine.disease Synovial sarcoma Leukemia 030104 developmental biology KMT2A medicine.anatomical_structure target validation Oncology Cell culture 030220 oncology & carcinogenesis Histone methyltransferase biology.protein Cancer research menin-MLL solid tumor |
Zdroj: | Cancers Volume 12 Issue 1 Cancers, Vol 12, Iss 1, p 201 (2020) |
ISSN: | 2072-6694 |
DOI: | 10.3390/cancers12010201 |
Popis: | Inhibiting the interaction of menin with the histone methyltransferase MLL1 (KMT2A) has recently emerged as a novel therapeutic strategy. Beneficial therapeutic effects have been postulated in leukemia, prostate, breast, liver and in synovial sarcoma models. In those indications, MLL1 recruitment by menin was described to critically regulate the expression of disease associated genes. However, most findings so far rely on single study reports. Here we independently evaluated the pathogenic functions of the menin-MLL interaction in a large set of different cancer models with a potent and selective probe inhibitor BAY-155. We characterized the inhibition of the menin-MLL interaction for anti-proliferation, gene transcription effects, and for efficacy in several in vivo xenografted tumor models. We found a specific therapeutic activity of BAY-155 primarily in AML/ALL models. In solid tumors, we observed anti-proliferative effects of BAY-155 in a surprisingly limited fraction of cell line models. These findings were further validated in vivo. Overall, our study using a novel, highly selective and potent inhibitor, shows that the menin-MLL interaction is not essential for the survival of most solid cancer models. We can confirm that disrupting the menin-MLL complex has a selective therapeutic benefit in MLL-fused leukemia. In solid cancers, effects are restricted to single models and more limited than previously claimed. |
Databáze: | OpenAIRE |
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