Arrigoni Chiara, Bersini Simone, Gilardi Mara, Moretti Matteo
Cell and Tissue Engineering Laboratory, IRCCS Istituto Ortopedico Galeazzi, via Galeazzi 4, 20161 Milano, Italy.
Department of Biotechnology and Biosciences, PhD School in Life Sciences, University of Milano-Bicocca, 20126 Milano, Italy.
Int J Mol Sci. 2016 Aug 25;17(9):1405. doi: 10.3390/ijms17091405.
Advanced breast cancer frequently metastasizes to bone through a multistep process involving the detachment of cells from the primary tumor, their intravasation into the bloodstream, adhesion to the endothelium and extravasation into the bone, culminating with the establishment of a vicious cycle causing extensive bone lysis. In recent years, the crosstalk between tumor cells and secondary organs microenvironment is gaining much attention, being indicated as a crucial aspect in all metastatic steps. To investigate the complex interrelation between the tumor and the microenvironment, both in vitro and in vivo models have been exploited. In vitro models have some advantages over in vivo, mainly the possibility to thoroughly dissect in controlled conditions and with only human cells the cellular and molecular mechanisms underlying the metastatic progression. In this article we will review the main results deriving from in vitro co-culture models, describing mechanisms activated in the crosstalk between breast cancer and bone cells which drive the different metastatic steps.
晚期乳腺癌常通过多步骤过程转移至骨,该过程包括肿瘤细胞从原发肿瘤脱离、进入血液循环、黏附于内皮细胞并外渗至骨,最终形成恶性循环导致广泛的骨质溶解。近年来,肿瘤细胞与继发器官微环境之间的相互作用备受关注,被认为是所有转移步骤中的关键因素。为了研究肿瘤与微环境之间的复杂相互关系,人们开发了体外和体内模型。体外模型相对于体内模型具有一些优势,主要在于能够在可控条件下,仅用人细胞深入剖析转移进展背后的细胞和分子机制。在本文中,我们将回顾体外共培养模型的主要研究结果,描述乳腺癌与骨细胞相互作用中激活的驱动不同转移步骤的机制。