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.
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
| 期刊: | Epigenomics | 影响因子: | 2.600 |
| 时间: | 2021 | 起止号: | 2021 Jan;13(2):129-144 |
| doi: | 10.2217/epi-2020-0189 | 靶点: | BCL2 |
| 研究方向: | 细胞生物学、表观遗传 | ||
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