Fregona Vincent, Bayet Manon, Gerby Bastien
Centre de Recherches en Cancérologie de Toulouse (CRCT), Université de Toulouse, Institut National de la Santé et de la Recherche Médicale (INSERM), UMR-1037, Université Toulouse III Paul Sabatier (UPS), 31100 Toulouse, France.
Cancers (Basel). 2021 Nov 2;13(21):5511. doi: 10.3390/cancers13215511.
Our understanding of the hierarchical structure of acute leukemia has yet to be fully translated into therapeutic approaches. Indeed, chemotherapy still has to take into account the possibility that leukemia-initiating cells may have a distinct chemosensitivity profile compared to the bulk of the tumor, and therefore are spared by the current treatment, causing the relapse of the disease. Therefore, the identification of the cell-of-origin of leukemia remains a longstanding question and an exciting challenge in cancer research of the last few decades. With a particular focus on acute lymphoblastic leukemia, we present in this review the previous and current concepts exploring the phenotypic, genetic and functional heterogeneity in patients. We also discuss the benefits of using engineered mouse models to explore the early steps of leukemia development and to identify the biological mechanisms driving the emergence of leukemia-initiating cells. Finally, we describe the major prospects for the discovery of new therapeutic strategies that specifically target their aberrant stem cell-like functions.
我们对急性白血病分层结构的理解尚未完全转化为治疗方法。事实上,化疗仍需考虑白血病起始细胞可能与肿瘤主体具有不同的化学敏感性特征,因此当前治疗对其无效,从而导致疾病复发。因此,白血病起源细胞的鉴定仍然是过去几十年来癌症研究中一个长期存在的问题和令人兴奋的挑战。本文特别关注急性淋巴细胞白血病,回顾了以往和当前探索患者表型、基因和功能异质性的概念。我们还讨论了使用工程小鼠模型探索白血病发展早期步骤以及识别驱动白血病起始细胞出现的生物学机制的益处。最后,我们描述了发现特异性靶向其异常干细胞样功能的新治疗策略的主要前景。