Lee John T, Herlyn Meenhard
The Wistar Institute, Program of Molecular and Cellular Oncogenesis, Philadelphia, PA 19104, USA.
J Cell Biochem. 2007 Jul 1;101(4):862-72. doi: 10.1002/jcb.21204.
An often overlooked facet of tumor biology research is the involvement of the surrounding tumor microenvironment. Increasing evidence is being presented to support a major role for stromal components in all stages of tumorigenesis including initiation, progression, and metastasis. Melanoma serves as a model for studying cellular and stromal interactions within the tumor microenvironment due to the array of cell types localized to these lesions. Here, we discuss the both the molecular mechanisms, as well as the extracellular and contextual input that contribute to melanoma progression. Special emphasis is given to the assorted cell types and their interactions with the extracellular matrix and adjacent cells. Melanoma progression also initiates development of intralesional hypoxic regions; the relative significance of hypoxia in disease is also addressed. Lastly, a number of laboratories are currently developing innovative strategies to study melanoma within a microenvironmental platform. These promising model systems and their potential for closing current gaps in knowledge of disease are reviewed. The development of such models holds translational value that cannot be achieved with most current systems.
肿瘤生物学研究中一个常常被忽视的方面是肿瘤周围微环境的作用。越来越多的证据表明,基质成分在肿瘤发生的各个阶段,包括起始、进展和转移中都发挥着重要作用。黑色素瘤由于其病变部位存在多种细胞类型,成为研究肿瘤微环境中细胞与基质相互作用的一个模型。在此,我们将讨论促成黑色素瘤进展的分子机制,以及细胞外和环境因素。特别强调了各种细胞类型及其与细胞外基质和相邻细胞的相互作用。黑色素瘤的进展还引发了瘤内缺氧区域的形成;文中也探讨了缺氧在疾病中的相对重要性。最后,目前许多实验室正在开发创新策略,以在微环境平台上研究黑色素瘤。本文综述了这些前景广阔的模型系统及其在填补当前疾病知识空白方面的潜力。此类模型的开发具有目前大多数系统无法实现的转化价值。