Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China; Key Laboratory of Stem Cells and Tissue Engineering (Ministry of Education), Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong.
Department of Pediatrics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong.
Haematologica. 2022 Oct 1;107(10):2344-2355. doi: 10.3324/haematol.2021.280290.
Chemotherapy is the primary treatment option for acute myeloid leukemia (AML), but leukemic stem cells (LSC) can survive chemotherapy for disease recurrence and refractory. Here, we found that AML cells obtained from relapsed patients had increased autophagy levels than de novo AML cells. Furthermore, doxorubicin (DOX) treatment stimulated autophagy in LSC by repressing the mTOR pathway, and pharmaceutical inhibition of autophagy rendered chemoresistant LSC sensitive to DOX treatment in MLL-AF9 induced murine AML. Moreover, we developed a self-assembled leucine polymer, which activated mTOR to inhibit autophagy in AML cells by releasing leucine. The leucine polymer loaded DOX (Leu-DOX) induced much less autophagy but more robust apoptosis in AML cells than the DOX treatment. Notably, the leucine polymer and Leu-DOX were specifically taken up by AML cells and LSC but not by normal hematopoietic cells and hematopoietic stem/progenitor cells in the bone marrow. Consequently, Leu-DOX efficiently reduced LSC and prolonged the survival of AML mice, with more limited myeloablation and tissue damage side effects than DOX treatment. Overall, we proposed that the newly developed Leu-DOX is an effective autophagy inhibitor and an ideal drug to efficiently eliminate LSC, thus serving as a revolutionary strategy to enhance the chemotherapy efficacy in AML.
化疗是急性髓系白血病(AML)的主要治疗选择,但白血病干细胞(LSC)可以在化疗后存活,导致疾病复发和耐药。在这里,我们发现来自复发患者的 AML 细胞比初发 AML 细胞具有更高的自噬水平。此外,多柔比星(DOX)通过抑制 mTOR 通路刺激 LSC 中的自噬,而自噬的药物抑制使耐药 LSC 对 MLL-AF9 诱导的小鼠 AML 中的 DOX 治疗敏感。此外,我们开发了一种自组装亮氨酸聚合物,通过释放亮氨酸激活 mTOR 以抑制 AML 细胞中的自噬。亮氨酸聚合物负载 DOX(Leu-DOX)在 AML 细胞中诱导的自噬少于 DOX 治疗,但诱导的细胞凋亡更强烈。值得注意的是,亮氨酸聚合物和 Leu-DOX 被 AML 细胞和 LSC 特异性摄取,但不被骨髓中的正常造血细胞和造血干/祖细胞摄取。因此,Leu-DOX 有效地减少了 LSC 并延长了 AML 小鼠的存活时间,与 DOX 治疗相比,其骨髓抑制和组织损伤副作用更为有限。总的来说,我们提出新开发的 Leu-DOX 是一种有效的自噬抑制剂,是一种理想的药物,可以有效地消除 LSC,从而为提高 AML 的化疗疗效提供了一种革命性的策略。