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Interfering with stem cell-specific gatekeeper functions controls tumour initiation and malignant progression of skin tumours

机译:干扰干细胞特有的网守功能可控制肿瘤的发生和皮肤肿瘤的恶性进展

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摘要

Epithelial cancer constitutes a major clinical challenge and molecular mechanisms underlying the process of tumour initiation are not well understood. Here we demonstrate that hair follicle bulge stem cells (SCs) give rise to well-differentiated sebaceous tumours and show that SCs are not only crucial in tumour initiation, but are also involved in tumour plasticity and heterogeneity. Our findings reveal that SC-specific expression of mutant Lef1, which mimics mutations found in human sebaceous tumours, drives sebaceous tumour formation. Mechanistically, we demonstrate that mutant Lef1 abolishes p53 activity in SCs. Intriguingly, mutant Lef1 induces DNA damage and interferes with SC-specific gatekeeper functions normally protecting against accumulations of DNA lesions and cell loss. Thus, normal control of SC proliferation is disrupted by mutant Lef1, thereby allowing uncontrolled propagation of tumour-initiating SCs. Collectively, these findings identify underlying molecular and cellular mechanisms of tumour-initiating events in tissue SCs providing a potential target for future therapeutic strategies.
机译:上皮癌构成了主要的临床挑战,对于肿瘤起始过程的分子机制尚不清楚。在这里,我们证明了毛囊隆突干细胞(SCs)引起了分化良好的皮脂腺肿瘤,并显示了SCs不仅在肿瘤起源中至关重要,而且还参与了肿瘤的可塑性和异质性。我们的研究结果表明,突变Lef1的SC特异性表达可模拟皮脂瘤的形成,该突变体模仿人皮脂瘤中发现的突变。从机制上讲,我们证明了突变Lef1废除了SC中的p53活性。有趣的是,突变体Lef1诱导DNA损伤并干扰SC特有的网守功能,该功能通常可防止DNA损伤的积累和细胞丢失。因此,突变体Lef1破坏了正常的SC增殖控制,从而导致肿瘤起始SC不受控制地传播。总的来说,这些发现确定了组织SC中肿瘤引发事件的潜在分子和细胞机制,为将来的治疗策略提供了潜在的靶标。

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