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恶性黑色素瘤研究的模型系统

Model Systems for the Study of Malignant Melanoma.

作者信息

Gregg Randal K

机构信息

Department of Basic Medical Sciences, DeBusk College of Osteopathic Medicine at Lincoln Memorial University-Knoxville, Knoxville, TN, USA.

出版信息

Methods Mol Biol. 2021;2265:1-21. doi: 10.1007/978-1-0716-1205-7_1.

Abstract

Since the first resection of melanoma by Hunter in 1787, efforts to treat patients with this deadly malignancy have been ongoing. Initial work to understand melanoma biology for therapeutics development began with the employment of isolated cancer cells grown in cell cultures. However, these models lack in vivo interactions with the tumor microenvironment. Melanoma cell line transplantation into suitable animals such as mice has been informative and useful for testing therapeutics as a preclinical model. Injection of freshly isolated patient melanomas into immunodeficient animals has shown the capacity to retain the genetic heterogeneity of the tumors, which is lost during the long-term culture of melanoma cells. Upon advancement of technology, genetically engineered animals have been generated to study the spontaneous development of melanomas in light of newly discovered genetic aberrations associated with melanoma formation. Culturing melanoma cells in a matrix generate tumor spheroids, providing an in vitro environment that promotes the heterogeneity commonplace with human melanoma and displaces the need for animal care facilities. Advanced 3D cultures have been created simulating the structure and cellularity of human skin to permit in vitro testing of therapeutics on melanomas expressing the same phenotype as demonstrated in vivo. This review will discuss these models and their relevance to the study of melanomagenesis, growth, metastasis, and therapy.

摘要

自1787年亨特首次切除黑色素瘤以来,针对这种致命恶性肿瘤患者的治疗努力一直在持续。为开发治疗方法而开展的关于黑色素瘤生物学的初步研究始于使用在细胞培养物中生长的分离癌细胞。然而,这些模型缺乏与肿瘤微环境的体内相互作用。将黑色素瘤细胞系移植到合适的动物(如小鼠)体内,作为临床前模型用于测试治疗方法,已颇具价值且很有用。将新鲜分离的患者黑色素瘤注射到免疫缺陷动物体内,已显示出其能够保留肿瘤的基因异质性,而这种异质性在黑色素瘤细胞的长期培养过程中会丧失。随着技术的进步,人们已培育出基因工程动物,以便根据新发现的与黑色素瘤形成相关的基因畸变来研究黑色素瘤的自发发展。在基质中培养黑色素瘤细胞可生成肿瘤球体,提供了一种体外环境,促进了人类黑色素瘤常见的异质性,并取代了对动物饲养设施的需求。已经创建了先进的3D培养模型,模拟人类皮肤的结构和细胞构成,以便在体外对与体内表现出相同表型的黑色素瘤进行治疗测试。本综述将讨论这些模型及其与黑色素瘤发生、生长、转移和治疗研究的相关性。

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