@article{b88eef1143ff416eb35227de09e41808,
title = "SOX2 is a cancer-specific regulator of tumour initiating potential in cutaneous squamous cell carcinoma",
abstract = "Although the principles that balance stem cell self-renewal and differentiation in normal tissue homeostasis are beginning to emerge, it is still unclear whether cancer cells with tumour initiating potential are similarly governed, or whether they have acquired distinct mechanisms to sustain self-renewal and long-term tumour growth. Here we show that the transcription factor Sox2, which is not expressed in normal skin epithelium and is dispensable for epidermal homeostasis, marks tumour initiating cells (TICs) in cutaneous squamous cell carcinomas (SCCs). We demonstrate that Sox2 is required for SCC growth in mouse and human, where it enhances Nrp1/Vegf signalling to promote the expansion of TICs along the tumour-stroma interface. Our findings suggest that distinct transcriptional programmes govern self-renewal and long-term growth of TICs and normal skin epithelial stem and progenitor cells. These programmes present promising diagnostic markers and targets for cancer-specific therapies.",
author = "Siegle, {Jasmin M.} and Alice Basin and Ana Sastre-Perona and Yoshiya Yonekubo and Jessie Brown and Rachel Sennett and Michael Rendl and Aristotelis Tsirigos and Carucci, {John A.} and Markus Schober",
note = "Funding Information: We thank Slobodan Beronja, Eva Hernando-Monge, Pedro Lee, Panagiotis Ntziachristos, Scott Williams and Eva Gonzalez for discussions and comments on the manuscript. We thank Elaine Fuchs for generous support and reagents, and Paul Khavari for LZRS-RasG12V. We are grateful for the help received from the NYU{\textquoteright}s Flow Cytometry, the Biorepository, Histology and Microscopy Core facilities (NCRR S10 RR024708), and NYU{\textquoteright}s Division of Laboratory Animal Resources, an ALAAC-accredited mouse facility, for their expert handling and care of the mice. This research was also supported by grants to M.S. by the National Institutes of Health R00-AR057260 and NIH/NCRR 1UL1RR029893-01.",
year = "2014",
month = jul,
day = "31",
doi = "10.1038/ncomms5511",
language = "English",
volume = "5",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "Nature Publishing Group",
}