Müller Ines, Kulms Dagmar
Experimental Dermatology, Medical Faculty, TU-Dresden.
Experimental Dermatology, Medical Faculty, TU-Dresden;
J Vis Exp. 2018 May 18(135):57500. doi: 10.3791/57500.
Malignant transformation of melanocytes, the pigment cells of human skin, causes formation of melanoma, a highly aggressive cancer with increased metastatic potential. Recently, mono-chemotherapies continue to improve by melanoma specific combination therapies with targeted kinase inhibitors. Still, metastatic melanoma remains a life-threatening disease because tumors exhibit primary resistance or develop resistance to novel therapies, thereby regaining tumorigenic capacity. In order to improve the therapeutic success of malignant melanoma, the determination of molecular mechanisms conferring resistance against conventional treatment approaches is necessary; however, it requires innovative cellular in vitro models. Here, we introduce an in vitro three-dimensional (3D) organotypic melanoma spheroid model that can portray the in vivo architecture of malignant melanoma and may warrant new insights into intra-tumoral as well as tumor-host interactions. The model incorporates defined numbers of mature and differentiated melanoma spheroids in a 3D human full skin reconstruction model consisting of primary skin cells. The cellular composition and differentiation status of the embedded melanoma spheroids is similar to the one of cutaneous melanoma metastasis in vivo. Using this organotypic melanoma spheroid model as a drug screening platform may support the identification of responders to selected combination therapies, while sparing the unnecessary treatment burden for non-responders, thereby increasing the benefit of therapeutic interventions.
人类皮肤色素细胞黑素细胞的恶性转化会导致黑色素瘤的形成,黑色素瘤是一种侵袭性很强的癌症,转移潜力增加。最近,单药化疗通过与靶向激酶抑制剂的黑色素瘤特异性联合疗法不断改进。然而,转移性黑色素瘤仍然是一种危及生命的疾病,因为肿瘤表现出原发性耐药或对新疗法产生耐药性,从而恢复致瘤能力。为了提高恶性黑色素瘤的治疗成功率,有必要确定赋予对传统治疗方法耐药性的分子机制;然而,这需要创新的细胞体外模型。在这里,我们介绍一种体外三维(3D)器官型黑色素瘤球体模型,该模型可以描绘恶性黑色素瘤的体内结构,并可能为肿瘤内以及肿瘤与宿主的相互作用提供新的见解。该模型在由原代皮肤细胞组成的3D人类全皮肤重建模型中纳入了确定数量的成熟和分化的黑色素瘤球体。嵌入的黑色素瘤球体的细胞组成和分化状态与体内皮肤黑色素瘤转移的情况相似。将这种器官型黑色素瘤球体模型用作药物筛选平台可能有助于识别对选定联合疗法有反应的患者,同时避免给无反应者带来不必要的治疗负担,从而增加治疗干预的益处。