Epigenetic targeting of Waldenström macroglobulinemia cells with BET inhibitors synergizes with BCL2 or histone deacetylase inhibition.

使用 BET 抑制剂对 Waldenström 巨球蛋白血症细胞进行表观遗传靶向治疗,可与 BCL2 或组蛋白去乙酰化酶抑制产生协同作用

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作者:Matissek Stephan J, Han Weiguo, Karbalivand Mona, Sayed Mohamed, Reilly Brendan M, Mallat Shayna, Ghazal Shimaa M, Munshi Manit, Yang Guang, Treon Steven P, Walker Sarah R, Elsawa Sherine F
Aim: Waldenström macroglobulinemia (WM) is a low-grade B-cell lymphoma characterized by overproduction of monoclonal IgM. To date, there are no therapies that provide a cure for WM patients, and therefore, it is important to explore new therapies. Little is known about the efficiency of epigenetic targeting in WM. Materials & methods: WM cells were treated with BET inhibitors (JQ1 and I-BET-762) and venetoclax, panobinostat or ibrutinib. Results: BET inhibition reduces growth of WM cells, with little effect on survival. This finding was enhanced by combination therapy, with panobinostat (LBH589) showing the highest synergy. Conclusion: Our studies identify BET inhibitors as effective therapy for WM, and these inhibitors can be enhanced in combination with BCL2 or histone deacetylase inhibition.

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