H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Cell Oncol (Dordr). 2011 Dec;34(6):545-51. doi: 10.1007/s13402-011-0060-6. Epub 2011 Oct 1.
Targeting of Notch signaling with γ-secretase inhibitors (GSIs) has been considered a promising strategy for the treatment of hematological malignancies including multiple myeloma (MM). Here we investigated whether the cytotoxic effect of bortezomib, an agent commonly used in MM, could be enhanced by the addition of a GSI.
MM cells were treated with GSI, bortezomib or the combination thereof. Apoptosis of MM cells, proteasome activity and Notch signaling activation were determined. The effect of the drug combination was also evaluated in MM cells transfected with the active domain of Notch-1.
Using MM cell lines and primary MM cells isolated from the bone marrow of patients with MM we found a strong synergistic effect of bortezomib in combination with one of the GSIs studied. We next investigated the mechanism underlying this synergistic effect and determined that the effect of the drug combination was mainly dependent on the ability of the selected GSI to inhibit proteasome activity in MM cells.
Our study demonstrates that selected GSIs that inhibit proteasome activity may be successfully used in combination with bortezomib enhancing its anti-MM effect.
用γ-分泌酶抑制剂(GSIs)靶向 Notch 信号已被认为是治疗包括多发性骨髓瘤(MM)在内的血液恶性肿瘤的一种很有前途的策略。在这里,我们研究了硼替佐米(一种常用于 MM 的药物)的细胞毒性作用是否可以通过添加 GSI 来增强。
用 GSI、硼替佐米或两者联合处理 MM 细胞。检测 MM 细胞的凋亡、蛋白酶体活性和 Notch 信号激活情况。还评估了该药物组合在转染 Notch-1 活性结构域的 MM 细胞中的作用。
通过使用 MM 细胞系和从 MM 患者骨髓中分离的原代 MM 细胞,我们发现硼替佐米与所研究的 GSI 之一联合具有很强的协同作用。我们接下来研究了这种协同作用的机制,并确定药物组合的作用主要取决于所选 GSI 抑制 MM 细胞蛋白酶体活性的能力。
我们的研究表明,抑制蛋白酶体活性的特定 GSI 可能与硼替佐米联合成功使用,增强其抗 MM 作用。