Center for Translational Science Activities, Mayo Clinic, Rochester, MN, USA.
Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Eur J Haematol. 2013 Dec;91(6):504-13. doi: 10.1111/ejh.12192. Epub 2013 Sep 17.
The introduction of novel immunomodulatory drugs (IMiDs) has dramatically improved the survival of patients with multiple myeloma (MM). While it has been shown that patients with specific cytogenetic subtypes, namely t(4;14), have the best outcomes when treated with bortezomib-based regimens, the relationship between cytogenetic subtypes and response to IMiDs remains unclear. Using DNA synthesis assays, we investigated the relationship between cytogenetic subtype and lenalidomide response in a representative panel of human myeloma cell lines (HMCLs). We examined HMCL protein expression levels of the lenalidomide target cereblon (CRBN) and its downstream target interferon regulatory factor-4 (IRF4), which have previously been shown to be predictive of lenalidomide response in HMCLs. Our results reveal that lenalidomide response did not correlate with specific cytogenetic translocations. There were distinct groups of lenalidomide-responsive and non-responsive HMCLs, as defined by inhibition of cellular proliferation; notably, all of the hyperdiploid HMCLs fell into the latter category. Repeated dosing of lenalidomide significantly lowered the IC50 of the responsive HMCL ALMC-1 (IC50 = 2.6 μm vs. 0.005 μm, P < 0.0001), but did not have an effect on the IC50 of the non-responsive DP-6 HMCL (P > 0.05). Moreover, no association was found between lenalidomide responsiveness and CRBN and IRF4 expression. Our data indicate that lenalidomide sensitivity is independent of cytogenetic subtype in HMCLs. While CRBN and IRF4 have been shown to be associated with response to lenalidomide in patients, these findings do not translate back to HMCLs, which could be attributable to factors present in the bone marrow microenvironment.
新型免疫调节药物(IMiDs)的引入显著改善了多发性骨髓瘤(MM)患者的生存。虽然已经表明,在用硼替佐米为基础的方案治疗时,具有特定细胞遗传学亚型的患者,即 t(4;14),具有最佳的预后,但细胞遗传学亚型与对 IMiDs 反应之间的关系仍不清楚。使用 DNA 合成测定法,我们在代表性的人骨髓瘤细胞系(HMCL)中研究了细胞遗传学亚型与来那度胺反应之间的关系。我们检查了来那度胺靶蛋白 cereblon(CRBN)及其下游靶蛋白干扰素调节因子-4(IRF4)的 HMCL 蛋白表达水平,这些蛋白之前已被证明可预测 HMCL 中对来那度胺的反应。我们的结果表明,来那度胺反应与特定的细胞遗传学易位无关。存在明显的来那度胺反应性和非反应性 HMCL 组,如细胞增殖抑制所定义;值得注意的是,所有超二倍体 HMCL 都属于后者。来那度胺的重复给药显着降低了反应性 HMCL ALMC-1 的 IC50(IC50 = 2.6 μm 对 0.005 μm,P <0.0001),但对非反应性 DP-6 HMCL 的 IC50 没有影响(P > 0.05)。此外,来那度胺反应性与 CRBN 和 IRF4 表达之间没有关联。我们的数据表明,在 HMCL 中,来那度胺敏感性与细胞遗传学亚型无关。虽然 CRBN 和 IRF4 已被证明与患者对来那度胺的反应相关,但这些发现不能转化回 HMCL,这可能归因于骨髓微环境中存在的因素。