A synthetic lethal screen identifies HDAC4 as a potential target in MELK overexpressing cancers

Author:

Zhou Lin,Zheng Siqi,Rosas Bringas Fernando R.,Bakker Bjorn,Simon Judith E.,Bakker Petra L.,Kazemier Hinke G.,Schubert MichaelORCID,Roorda MauritsORCID,van Vugt Marcel,Chang MichaelORCID,Foijer FlorisORCID

Abstract

AbstractMaternal embryonic leucine zipper kinase (MELK) is frequently overexpressed in cancer, but the role of MELK in cancer is still poorly understood. MELK was shown to have roles in many cancer-associated processes including tumor growth, chemotherapy resistance, and tumor recurrence. To determine whether the frequent overexpression of MELK can be exploited in therapy, we performed a high-throughput screen using a library of Saccharomyces cerevisiae mutants to identify genes whose functions become essential when MELK is overexpressed. We identified two such genes: LAG2 and HDA3. LAG2 encodes an inhibitor of the SCF ubiquitin-ligase complex, while HDA3 encodes a subunit of the HDA1 histone deacetylase complex. We find that one of these synthetic lethal interactions is conserved in mammalian cells, as inhibition of a human homolog of HDA3 (HDAC4) is synthetically toxic in MELK overexpression cells. Altogether, our work might provide a new angle of how to exploit MELK overexpression in cancers and might thus lead to novel intervention strategies.

Publisher

Cold Spring Harbor Laboratory

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