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10.1080/21541248.2016.1182242

http://scihub22266oqcxt.onion/10.1080/21541248.2016.1182242
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C5003544!5003544!27111451
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suck abstract from ncbi


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pmid27111451      Small+GTPases 2016 ; 7 (3): 147-55
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  • Oncogenic Ras: A double-edged sword for human epidermal stem and transient amplifying cells #MMPMID27111451
  • Dellambra E
  • Small GTPases 2016[Jul]; 7 (3): 147-55 PMID27111451show ga
  • The human epidermal clonal evolution, i.e. the transition from stem cells (SCs) to transient amplifying (TA)-cells and post-mitotic cells, is a continuous and tightly regulated process that ensures physiologic tissue homeostasis. The Ras family of small GTPases has a key role in skin homeostasis and tumorigenesis. Indeed, activating mutations in Ras genes have been found in human cutaneous squamous cell carcinomas (cSCCs) and in experimentally-induced murine cSCCs. In mouse models, the Ras signaling might lead to hyperproliferative phenotypes, including the development of cSCCs, depending on the nature of the founding cells. Tumor-initiating cells or Cancer Stem Cells (CSCs) have been demonstrated in murine and human cSCCs even if the mechanism of their development from normal SCs or TA-cells is not completely elucidated. Here, the relation between the Ras expression outcome and the clonogenic potential of the target keratinocyte is discussed.
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