Histone deacetylase inhibition in combination with MEK or BCL-2 inhibition in multiple myeloma

• Published in: Haematologica (Roma) Vol. 104; no. 10; pp. 2061 - 2074
• Main Authors: Ramakrishnan, Vijay G, Miller, Kevin C, Macon, Elaine P, Kimlinger, Teresa K, Haug, Jessica, Kumar, Sanjay, Gonsalves, Wilson I, Rajkumar, S Vincent, Kumar, Shaji K
• Format: Journal Article
• Language: English
• Published: Italy Ferrata Storti Foundation 01.10.2019
• ISSN: 0390-6078; 1592-8721
• DOI: 10.3324/haematol.2018.211110

Despite recent advances in the treatment of multiple myeloma, patients with this disease still inevitably relapse and become refractory to existing therapies. Mutations in , and are common in multiple myeloma, affecting 50% of patients at diagnosis and >70% at relapse. However, targeting mutated via MEK inhibition is merely cytostatic in myeloma and largely ineffective in the clinic. We examined mechanisms mediating this resistance and identified histone deacetylase inhibitors as potent synergistic partners. Combining the MEK inhibitor AZD6244 (selumetinib) with the pan-histone deacetylase inhibitor LBH589 (panobinostat) induced synergistic apoptosis in mutated multiple myeloma cell lines. Interestingly, this synergy was dependent on the pro-apoptotic protein BIM. We determined that while single-agent MEK inhibition increased BIM levels, the protein remained sequestered by antiapoptotic BCL-2 family members. LBH589 dissociated BIM from MCL-1 and BCL-X , which allowed it to bind BAX/BAK and thereby initiate apoptosis. The AZD6244/LBH589 combination was specifically active in cell lines with more BIM:MCL-1 complexes at baseline; resistant cell lines had more BIM:BCL-2 complexes. Those resistant cell lines were synergistically killed by combining the BH3 mimetic ABT-199 (venetoclax) with LBH589. Using more specific histone deacetylase inhibitors, i.e. MS275 (entinostat) and FK228 (romidepsin), and genetic methods, we determined that concomitant inhibition of histone deacetylases 1 and 2 was sufficient to synergize with either MEK or BCL-2 inhibition. Furthermore, these drug combinations effectively killed plasma cells from myeloma patients Given the preponderance of mutations, and the fact that ABT-199 has demonstrated clinical efficacy in relapsed/refractory multiple myeloma, these drug combinations hold prom ise as biomarker-driven therapies.