Royal University Hospital, Saskatoon, Canada.
Division of Pediatric Hematology, Oncology and Transplant, POETIC Laboratory for Novel Therapeutics Discovery in Pediatric Oncology, Alberta Children's Hospital, Calgary, Canada.
Stem Cells Dev. 2019 Oct 1;28(19):1277-1287. doi: 10.1089/scd.2019.0035. Epub 2019 Sep 17.
Although treatment strategies for pediatric leukemia have improved overall survival rates in the recent past, relapse rates in certain subgroups such as infant leukemia remain unacceptably high. Despite undergoing extensive chemotherapy designed to target the rapidly proliferating leukemia cells, many of these children experience relapse. In refractory leukemia, the existence of cell populations with stemness characteristics, termed leukemia stem cells (LSCs), which remain quiescent and subsequently replenish the blast population, has been described. A significant body of evidence exists, derived largely from xenograft models of adult acute myeloid leukemia, to support the idea that LSCs may play a fundamental role in refractory disease. In addition, clinical studies have also linked LSCs with increased minimal residual disease, higher relapse rate, and decreased survival rates in these patients. Recently, a number of reports have addressed effective ways to utilize new-generation genomic sequencing and transcriptomic analyses to identify targeted therapeutic agents aimed at LSCs, while sparing normal hematopoietic stem cells. These data underscore the value of timely translation of knowledge from adult studies to the unique molecular and physiological characteristics seen in pediatric leukemia. We aim to summarize this article in the rapidly expanding field of stem cell biology in hematopoietic malignancies, focusing particularly on relevant preclinical models and novel targeted therapeutics, and their applicability to childhood leukemia.
尽管儿科白血病的治疗策略在最近一段时间内提高了总体生存率,但某些亚组(如婴儿白血病)的复发率仍然高得令人无法接受。尽管接受了旨在针对快速增殖的白血病细胞的广泛化疗,但许多儿童仍会复发。在难治性白血病中,存在具有干性特征的细胞群体,称为白血病干细胞(LSCs),这些细胞保持静止并随后补充成白血病细胞。大量来自成人急性髓细胞白血病异种移植模型的证据支持 LSCs 可能在难治性疾病中起关键作用的观点。此外,临床研究还将 LSCs 与增加的微小残留疾病、更高的复发率和这些患者的生存率降低联系起来。最近,有许多报道探讨了利用新一代基因组测序和转录组分析来识别针对 LSCs 的靶向治疗药物的有效方法,同时保留正常造血干细胞。这些数据强调了及时将成人研究中的知识转化为儿科白血病中独特的分子和生理特征的价值。我们旨在总结这篇文章在造血恶性肿瘤中快速发展的干细胞生物学领域,特别关注相关的临床前模型和新型靶向治疗药物,以及它们在儿童白血病中的适用性。