Developmental Therapeutics Program, Institute for Peadiatric Clinical Research, Childrens Hospital Los Angeles, and Department of Pediatrics, University of Southern California, Keck School of Medicine, Los Angeles, CA 90027-0367, USA.
Br J Haematol. 2010 May;149(4):508-17. doi: 10.1111/j.1365-2141.2010.08106.x. Epub 2010 Feb 11.
The present study found that the pentapeptide mimic C-61, targeting the substrate binding P-site of SYK tyrosine kinase acted as a potent inducer of apoptosis in chemotherapy-resistant SYK-expressing primary leukemic B-cell precursors taken directly from relapsed B-precursor leukaemia (BPL) patients (but not SYK-deficient infant pro-B leukaemia cells), exhibited favourable pharmacokinetics in mice and non-human primates, and eradicated in vivo clonogenic leukaemia cells in severe combined immunodeficient mouse xenograft models of chemotherapy-resistant human BPL at dose levels non-toxic to mice and non-human primates. These in vitro and in vivo findings provide proof of principle for effective treatment of chemotherapy-resistant BPL by targeting SYK-dependent anti-apoptotic blast cell survival machinery with a SYK P-Site inhibitor. Further development of C-61 may provide the foundation for therapeutic innovation against chemotherapy-resistant BPL.
本研究发现,五肽模拟物 C-61 靶向 SYK 酪氨酸激酶的底物结合 P 位,可作为一种有效的诱导剂,诱导源自复发 B 前体细胞白血病 (BPL) 患者的化疗耐药 SYK 表达原发性白血病 B 细胞前体(而非 SYK 缺陷的婴儿前 B 细胞白血病细胞)发生细胞凋亡,在小鼠和非人类灵长类动物中具有良好的药代动力学特性,并且在化疗耐药人类 BPL 的严重联合免疫缺陷小鼠异种移植模型中,在对小鼠和非人类灵长类动物无毒的剂量水平下消除体内克隆性白血病细胞。这些体外和体内研究结果为通过靶向 SYK 依赖性抗凋亡母细胞存活机制用 SYK P 位抑制剂治疗化疗耐药 BPL 提供了原理证明。进一步开发 C-61 可能为治疗化疗耐药 BPL 的治疗创新提供基础。