Department of Biochemistry and Cancer Institute, West Virginia University Health Sciences Center, One Medical Center Drive, Morgantown, WV, USA.
Department of Biology, Shepherd University, Shepherdstown, WV, USA.
Adv Exp Med Biol. 2019;1139:105-114. doi: 10.1007/978-3-030-14366-4_6.
Metastatic melanoma continues to present a significant challenge-with a cure rate of less than 10% and a median survival of 6-9 months. Despite noteworthy advances in the field, the heterogeneity of melanoma tumors, comprised of cell subpopulations expressing a cancer stem cell (CSC) phenotype concomitant with drug resistance markers presents a formidable challenge in the design of current therapies. Particularly vexing is the ability of distinct subpopulations of melanoma cells to resist standard-of-care treatments, resulting in relapse and progression to metastasis. Recent studies have provided new information and insights into the expression and function of CSC markers associated with the aggressive melanoma phenotype, such as the embryonic morphogen Nodal and CD133, together with a drug resistance marker ABCA1. This chapter highlights major findings that demonstrate the promise of targeting Nodal as a viable option to pursue in combination with standard-of-care therapy. In recognizing that aggressive melanoma tumors utilize multiple mechanisms to survive, we must consider a more strategic approach to effectively target heterogeneity, tumor cell plasticity, and functional adaptation and resistance to current therapies-to eliminate relapse, disease progression, and metastasis.
转移性黑色素瘤仍然是一个重大挑战,治愈率不到 10%,中位生存期为 6-9 个月。尽管该领域取得了显著进展,但黑色素瘤肿瘤的异质性,由表达癌症干细胞 (CSC) 表型的细胞亚群与耐药标志物共同构成,给当前疗法的设计带来了巨大挑战。特别令人烦恼的是,不同亚群的黑色素瘤细胞能够抵抗标准治疗,导致复发和转移进展。最近的研究为与侵袭性黑色素瘤表型相关的 CSC 标志物的表达和功能提供了新的信息和见解,例如胚胎形态发生素 Nodal 和 CD133,以及耐药标志物 ABCA1。本章重点介绍了主要发现,这些发现表明靶向 Nodal 作为一种可行的选择与标准治疗联合应用具有广阔的前景。在认识到侵袭性黑色素瘤肿瘤利用多种机制来存活的同时,我们必须考虑采取更具战略性的方法来有效靶向异质性、肿瘤细胞可塑性以及对现有疗法的功能适应和耐药性,以消除复发、疾病进展和转移。