Gerby Bastien, Tremblay Cedric S, Tremblay Mathieu, Rojas-Sutterlin Shanti, Herblot Sabine, Hébert Josée, Sauvageau Guy, Lemieux Sébastien, Lécuyer Eric, Veiga Diogo F T, Hoang Trang
Institute of Research in Immunology and Cancer - University of Montreal, Montreal, Quebec, Canada; Molecular Biology Program, Faculty of Medicine, University of Montreal, Montreal, Quebec, Canada.
Institute of Research in Immunology and Cancer - University of Montreal, Montreal, Quebec, Canada.
PLoS Genet. 2014 Dec 18;10(12):e1004768. doi: 10.1371/journal.pgen.1004768. eCollection 2014 Dec.
The molecular determinants that render specific populations of normal cells susceptible to oncogenic reprogramming into self-renewing cancer stem cells are poorly understood. Here, we exploit T-cell acute lymphoblastic leukemia (T-ALL) as a model to define the critical initiating events in this disease. First, thymocytes that are reprogrammed by the SCL and LMO1 oncogenic transcription factors into self-renewing pre-leukemic stem cells (pre-LSCs) remain non-malignant, as evidenced by their capacities to generate functional T cells. Second, we provide strong genetic evidence that SCL directly interacts with LMO1 to activate the transcription of a self-renewal program coordinated by LYL1. Moreover, LYL1 can substitute for SCL to reprogram thymocytes in concert with LMO1. In contrast, inhibition of E2A was not sufficient to substitute for SCL, indicating that thymocyte reprogramming requires transcription activation by SCL-LMO1. Third, only a specific subset of normal thymic cells, known as DN3 thymocytes, is susceptible to reprogramming. This is because physiological NOTCH1 signals are highest in DN3 cells compared to other thymocyte subsets. Consistent with this, overexpression of a ligand-independent hyperactive NOTCH1 allele in all immature thymocytes is sufficient to sensitize them to SCL-LMO1, thereby increasing the pool of self-renewing cells. Surprisingly, hyperactive NOTCH1 cannot reprogram thymocytes on its own, despite the fact that NOTCH1 is activated by gain of function mutations in more than 55% of T-ALL cases. Rather, elevating NOTCH1 triggers a parallel pathway involving Hes1 and Myc that dramatically enhances the activity of SCL-LMO1 We conclude that the acquisition of self-renewal and the genesis of pre-LSCs from thymocytes with a finite lifespan represent a critical first event in T-ALL. Finally, LYL1 and LMO1 or LMO2 are co-expressed in most human T-ALL samples, except the cortical T subtype. We therefore anticipate that the self-renewal network described here may be relevant to a majority of human T-ALL.
使特定群体的正常细胞易受致癌重编程转化为自我更新的癌症干细胞的分子决定因素,目前还知之甚少。在此,我们利用T细胞急性淋巴细胞白血病(T-ALL)作为模型来定义该疾病中的关键起始事件。首先,被SCL和LMO1致癌转录因子重编程为自我更新的白血病前期干细胞(pre-LSCs)的胸腺细胞仍保持非恶性,这可由它们产生功能性T细胞的能力得到证明。其次,我们提供了有力的遗传学证据,表明SCL直接与LMO1相互作用,以激活由LYL1协调的自我更新程序的转录。此外,LYL1可以与LMO1协同替代SCL对胸腺细胞进行重编程。相比之下,抑制E2A不足以替代SCL,这表明胸腺细胞重编程需要SCL-LMO1的转录激活。第三,只有正常胸腺细胞的一个特定亚群,即DN3胸腺细胞,易受重编程影响。这是因为与其他胸腺细胞亚群相比,生理状态下的NOTCH1信号在DN3细胞中最高。与此一致的是,在所有未成熟胸腺细胞中过表达一种配体非依赖性的高活性NOTCH1等位基因足以使它们对SCL-LMO1敏感,从而增加自我更新细胞的数量。令人惊讶的是,尽管在超过55%的T-ALL病例中NOTCH1通过功能获得性突变被激活,但高活性的NOTCH1自身并不能对胸腺细胞进行重编程。相反,提高NOTCH1会触发一条涉及Hes1和Myc的平行途径,该途径会显著增强SCL-LMO1的活性。我们得出结论,具有有限寿命的胸腺细胞获得自我更新能力以及白血病前期干细胞的产生是T-ALL中的关键首个事件。最后,除皮质T亚型外,LYL1和LMO1或LMO2在大多数人类T-ALL样本中共同表达。因此,我们预计这里描述的自我更新网络可能与大多数人类T-ALL相关。