Characterization of a PERK Kinase Inhibitor with Anti-Myeloma Activity

• Published in: Cancers Vol. 12; no. 10; p. 2864
• Main Authors: Bagratuni, Tina, Patseas, Dimitrios, Mavrianou-Koutsoukou, Nefeli, Liacos, Christine Ivy, Sklirou, Aimilia D., Rousakis, Pantelis, Gavriatopoulou, Maria, Terpos, Evangelos, Tsitsilonis, Ourania E., Trougakos, Ioannis P., Kastritis, Efstathios, Dimopoulos, Meletios A.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 05.10.2020; MDPI
• Subjects: Apoptosis; Bone cancer; Bone marrow; Bortezomib; Cell death; Cell growth; Cell proliferation; Chemoresistance; Chemotherapy; Drug development; eIF-2 kinase; Endoplasmic reticulum; Enzyme inhibitors; Gene expression; Health aspects; Investigations; Kinases; Multiple myeloma; Phenotypes; Phosphorylation; Phosphotransferases; Plasma; Plasma cells; Proteasome inhibitors; Protein expression; Protein folding; Protein kinase R; Protein-serine/threonine kinase; Transcription factors; Tumors; Germany
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers12102864

Due to increased immunoglobulin production and uncontrolled proliferation, multiple myeloma (MM) plasma cells develop a phenotype of deregulated unfolded protein response (UPR). The eIF2-alpha kinase 3 [EIF2αK3, protein kinase R (PKR)-like ER kinase (PERK)], the third known sensor of endoplasmic reticulum (ER) stress, is a serine-threonine kinase and, like the other two UPR-related proteins, i.e., IRE1 and ATF6, it is bound to the ER membrane. MM, like other tumors showing uncontrolled protein secretion, is highly dependent to UPR for survival; thus, inhibition of PERK can be an effective strategy to suppress growth of malignant plasma cells. Here, we have used GSK2606414, an ATP-competitive potent PERK inhibitor, and found significant anti-proliferative and apoptotic effects in a panel of MM cell lines. These effects were accompanied by the downregulation of key components of the PERK pathway as well as of other UPR elements. Consistently, PERK gene expression silencing significantly increased cell death in MM cells, highlighting the importance of PERK signaling in MM biology. Moreover, GSK2606414, in combination with the proteasome inhibitor bortezomib, exerted an additive toxic effect in MM cells. Overall, our data suggest that PERK inhibition could represent a novel combinatorial therapeutic approach in MM.