癌症干细胞
干细胞
癌症研究
NK-92
抗辐射性
黑色素瘤
川东北117
生物
淋巴因子激活杀伤细胞
免疫学
白细胞介素21
细胞培养
细胞生物学
T细胞
免疫系统
川地34
遗传学
作者
Gabriella Pietra,Claudia Manzini,Massimo Vitale,Maria Luisa Balsamo,Emanuela Ognio,Monica Boitano,Paola Queirolo,Lorenzo Moretta,M. C. Mingari
标识
DOI:10.1093/intimm/dxp047
摘要
Experimental and clinical data suggest that tumours harbour a cell population retaining stem cell characteristics that can drive tumorigenesis. CD133 is considered an important cancer stem cells (CSC)-associated marker. In a large variety of human malignancies, including melanoma, CD133+ cells have been reported to comprise CSC. In this study, we show that melanoma cell lines are highly heterogeneous for the expression of several stem cell-associated markers including CD133, c-kit/CD117 and p75 neurotrophin receptor/CD271. Since no information is available on the ability of NK cells to recognize and lyse melanoma stem cells, we assessed whether melanoma cell lines, characterized by stem cell-like features, were susceptible to lysis by IL-2-activated NK cells. We show that activated NK cells efficiently kill malignant melanoma cell lines that were enriched in putative CSC by the use of different selection methods (i.e. CD133 expression, radioresistance or the ability to form melanospheres in stem cell-supportive medium). NK cell-mediated recognition and lysis of melanoma cells involved different combinations of activating NK receptors. Since CSC have been reported to be both drug resistant and radioresistant, our present data suggest that NK-based adoptive immunotherapy could represent a novel therapeutic approach to possibly eradicate metastatic melanoma.
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