Abel Ethan V, Aplin Andrew E
Department of Cancer Biology and Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Front Biosci (Schol Ed). 2011 Jun 1;3(3):937-45. doi: 10.2741/198.
Melanoma is an exceptionally aggressive cancer with limited treatment options. As such, the idea that a minority of tumor cells, termed melanoma stem cells, are actually responsible for the progression of the disease offers up new possibilities for targeted therapies. However, reliable identification of these melanoma stem cells is complicated by the lack of clearly defined markers to distinguish them from the general tumor cell population. Additionally, there is evidence that under permissive conditions, a high proportion of melanoma cells are capable of forming tumors in mice. This review summarizes a number of the possible markers being considered for identifying melanoma stem cells, the potential role of transcription factors that regulate pluripotency and stem cell maintenance in melanoma, and evidence that may undermine the applicability of the cancer stem cell hypothesis to melanoma.
黑色素瘤是一种极具侵袭性的癌症,治疗选择有限。因此,少数被称为黑色素瘤干细胞的肿瘤细胞实际上是导致疾病进展的原因这一观点为靶向治疗提供了新的可能性。然而,由于缺乏明确的标志物来将这些黑色素瘤干细胞与一般肿瘤细胞群体区分开来,可靠地识别它们变得很复杂。此外,有证据表明,在适宜条件下,很大比例的黑色素瘤细胞能够在小鼠体内形成肿瘤。本综述总结了一些被考虑用于识别黑色素瘤干细胞的可能标志物、调节黑色素瘤多能性和干细胞维持的转录因子的潜在作用,以及可能削弱癌症干细胞假说在黑色素瘤中适用性的证据。