Leonard M Kathryn, Pamidimukkala Nidhi, Puts Gemma S, Snyder Devin E, Slominski Andrzej T, Kaetzel David M
Department of Biochemistry and Molecular Biology, School of Medicine, University of Maryland-Baltimore, Baltimore, MD 21201, USA.
University of Maryland Greenebaum Comprehensive Cancer Center, University of Maryland-Baltimore, Baltimore, MD 21201, USA.
Int J Mol Sci. 2017 Jul 28;18(8):1647. doi: 10.3390/ijms18081647.
Cutaneous malignant melanoma is an aggressive and potentially lethal form of skin cancer, particularly in its advanced and therapy-resistant stages, and the need for novel therapeutics and prognostic tools is acute. Incidence of melanoma has steadily increased over the past few decades, with exposure to the genome-damaging effects of ultraviolet radiation (UVR) well-recognized as a primary cause. A number of genetically-engineered mouse models (GEMMs) have been created that exhibit high incidence of spontaneous and induced forms of melanoma, and a select subset recapitulates its progression to aggressive and metastatic forms. These GEMMs hold considerable promise for providing insights into advanced stages of melanoma, such as potential therapeutic targets and prognostic markers, and as in vivo systems for testing of novel therapies. In this review, we summarize how the HGF/SF transgenic mouse has been used to reveal metastasis-regulating activity of four different genes (, and ) in the context of UV-induced melanoma. We also discuss how these models can potentially yield new strategies for clinical management of melanoma in its most aggressive forms.
皮肤恶性黑色素瘤是一种侵袭性且可能致命的皮肤癌形式,尤其是在其晚期和抗治疗阶段,对新型治疗方法和预后工具的需求十分迫切。在过去几十年中,黑色素瘤的发病率稳步上升,暴露于紫外线辐射(UVR)对基因组的破坏作用被公认为主要原因。已经创建了许多基因工程小鼠模型(GEMMs),这些模型表现出自发性和诱导性黑色素瘤的高发病率,并且有一部分模型概括了其向侵袭性和转移性形式的进展。这些GEMMs在深入了解黑色素瘤的晚期阶段(如潜在治疗靶点和预后标志物)以及作为测试新型疗法的体内系统方面具有很大的前景。在这篇综述中,我们总结了HGF/SF转基因小鼠如何被用于揭示在紫外线诱导的黑色素瘤背景下四种不同基因(、和)的转移调节活性。我们还讨论了这些模型如何有可能为最具侵袭性形式的黑色素瘤临床管理产生新策略。