| Literature DB >> 25262208 |
Irene Miranda-Lorenzo1, Jorge Dorado1, Enza Lonardo1, Sonia Alcala1, Alicia G Serrano2, Jenifer Clausell-Tormos1, Michele Cioffi1, Diego Megias3, Sladjana Zagorac1, Anamaria Balic1, Manuel Hidalgo4, Mert Erkan5, Joerg Kleeff5, Aldo Scarpa6, Bruno Sainz1, Christopher Heeschen7.
Abstract
Cancer stem cells (CSCs) are thought to drive tumor growth, metastasis and chemoresistance. Although surface markers such as CD133 and CD44 have been successfully used to isolate CSCs, their expression is not exclusively linked to the CSC phenotype and is prone to environmental alteration. We identified cells with an autofluorescent subcellular compartment that exclusively showed CSC features across different human tumor types. Primary tumor-derived autofluorescent cells did not overlap with side-population (SP) cells, were enriched in sphere culture and during chemotherapy, strongly expressed pluripotency-associated genes, were highly metastatic and showed long-term in vivo tumorigenicity, even at the single-cell level. Autofluorescence was due to riboflavin accumulation in membrane-bounded cytoplasmic structures bearing ATP-dependent ABCG2 transporters. In summary, we identified and characterized an intrinsic autofluorescent phenotype in CSCs of diverse epithelial cancers and used this marker to isolate and characterize these cells.Entities:
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Year: 2014 PMID: 25262208 DOI: 10.1038/nmeth.3112
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547