Paul O'Gorman Leukaemia Research Centre, Medical Faculty, University of Glasgow, Glasgow, United Kingdom.
Blood. 2010 Mar 18;115(11):2241-50. doi: 10.1182/blood-2008-06-164582. Epub 2010 Jan 12.
Chronic myeloid leukemia (CML) is treated effectively with tyrosine kinase inhibitors (TKIs); however, 2 key problems remain-the insensitivity of CML stem and progenitor cells to TKIs and the emergence of TKI-resistant BCR-ABL mutations. BCR-ABL activity is associated with increased proteasome activity and proteasome inhibitors (PIs) are cytotoxic against CML cell lines. We demonstrate that bortezomib is antiproliferative and induces apoptosis in chronic phase (CP) CD34+ CML cells at clinically achievable concentrations. We also show that bortezomib targets primitive CML cells, with effects on CD34+38(-), long-term culture-initiating (LTC-IC) and nonobese diabetic/severe combined immunodeficient (NOD/SCID) repopulating cells. Bortezomib is not selective for CML cells and induces apoptosis in normal CD34+38(-) cells. The effects against CML cells are seen when bortezomib is used alone and in combination with dasatinib. Bortezomib causes proteasome but not BCR-ABL inhibition and is also effective in inhibiting proteasome activity and inducing apoptosis in cell lines expressing BCR-ABL mutations, including T315I. By targeting both TKI-insensitive stem and progenitor cells and TKI-resistant BCR-ABL mutations, we believe that bortezomib offers a potential therapeutic option in CML. Because of known toxicities, including myelosuppression, the likely initial clinical application of bortezomib in CML would be in resistant and advanced disease.
慢性髓性白血病(CML)可以通过酪氨酸激酶抑制剂(TKI)有效地治疗;然而,仍存在 2 个关键问题——CML 干细胞和祖细胞对 TKI 的不敏感性,以及 TKI 耐药 BCR-ABL 突变的出现。BCR-ABL 的活性与蛋白酶体活性的增加有关,蛋白酶体抑制剂(PIs)对 CML 细胞系具有细胞毒性。我们证明硼替佐米在临床上可达到的浓度下对慢性期(CP)CD34+CML 细胞具有抗增殖作用,并诱导其凋亡。我们还表明,硼替佐米靶向原始 CML 细胞,对 CD34+38(-)、长期培养起始(LTC-IC)和非肥胖型糖尿病/严重联合免疫缺陷(NOD/SCID)重建细胞有作用。硼替佐米对 CML 细胞不是选择性的,并且在正常 CD34+38(-)细胞中诱导凋亡。硼替佐米单独使用和与 dasatinib 联合使用时,对 CML 细胞的作用可见。硼替佐米引起蛋白酶体而不是 BCR-ABL 抑制,并且在表达 BCR-ABL 突变的细胞系中,包括 T315I,也能有效抑制蛋白酶体活性并诱导其凋亡。通过靶向 TKI 不敏感的干细胞和祖细胞以及 TKI 耐药的 BCR-ABL 突变,我们认为硼替佐米为 CML 提供了一种潜在的治疗选择。由于已知的毒性,包括骨髓抑制,硼替佐米在 CML 中的可能初始临床应用将是在耐药和晚期疾病中。