Université Libre de Bruxelles (ULB), IRIBHM, Brussels B-1070, Belgium.
Nat Cell Biol. 2010 Mar;12(3):299-305. doi: 10.1038/ncb2031. Epub 2010 Feb 14.
For most types of cancers, the cell at the origin of tumour initiation is still unknown. Here, we used mouse genetics to identify cells at the origin of basal cell carcinoma (BCC), which is one of the most frequently occurring types of cancer in humans, and can result from the activation of the Hedgehog signalling pathway. Using mice conditionally expressing constitutively active Smoothened mutant (SmoM2), we activated Hedgehog signalling in different cellular compartments of the skin epidermis and determined in which compartments Hedgehog activation induces BCC formation. Activation of SmoM2 in hair follicle bulge stem cells and their transient amplifying progenies did not induce cancer formation, demonstrating that BCC does not originate from bulge stem cells, as previously thought. Using clonal analysis, we found that BCC arises from long-term resident progenitor cells of the interfollicular epidermis and the upper infundibulum. Our studies uncover the cells at the origin of BCC in mice and demonstrate that expression of differentiation markers in tumour cells is not necessarily predictive of the cancer initiating cells.
对于大多数类型的癌症来说,肿瘤起始的细胞仍然未知。在这里,我们使用小鼠遗传学来鉴定基底细胞癌 (BCC) 的起始细胞,BCC 是人类最常见的癌症类型之一,可由 Hedgehog 信号通路的激活引起。我们使用条件表达组成型激活 Smoothened 突变体 (SmoM2) 的小鼠,在皮肤表皮的不同细胞区室中激活 Hedgehog 信号,并确定在哪些区室中 Hedgehog 激活诱导 BCC 形成。Hedgehog 信号在毛囊隆突干细胞及其短暂扩增后代中的激活并未诱导癌症形成,这表明 BCC 并非起源于以前认为的隆突干细胞。通过克隆分析,我们发现 BCC 起源于毛囊间表皮和上部漏斗的长期驻留祖细胞。我们的研究揭示了小鼠中 BCC 的起始细胞,并表明肿瘤细胞中分化标志物的表达不一定能预测癌症起始细胞。