Cancer Stem Cell Section, Laboratory of Cancer Prevention, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.
Stem Cells. 2010 Mar 31;28(3):390-8. doi: 10.1002/stem.271.
There is mounting evidence that tumors are initiated by a rare subset of cells called cancer stem cells (CSCs). CSCs are generally quiescent, self-renew, form tumors at low numbers, and give rise to the heterogeneous cell types found within a tumor. CSCs isolated from multiple tumor types differentiate both in vivo and in vitro when cultured in serum, yet the factors responsible for their differentiation have not yet been identified. Here we show that vitronectin is the component of human serum driving stem cell differentiation through an integrin alpha V beta 3-dependent mechanism. CSCs cultured on vitronectin result in downregulation of stem cell genes, modulation of differentiation markers, and loss of beta-catenin nuclear localization. Blocking integrin alpha V beta 3 inhibits differentiation and subsequently tumor formation. Thus, CSCs must be engaged by one or more extracellular signals to differentiate and initiate tumor formation, defining a new axis for future novel therapies aimed at both the extrinsic and intracellular pathways.
越来越多的证据表明,肿瘤是由一种称为癌症干细胞(CSC)的罕见细胞亚群引发的。CSC 通常处于静止状态,自我更新,以低数量形成肿瘤,并产生肿瘤内发现的异质细胞类型。从多种肿瘤类型中分离出的 CSC 在血清中培养时,无论是在体内还是在体外都能分化,但负责其分化的因素尚未确定。在这里,我们表明,纤连蛋白是通过整合素 αVβ3 依赖性机制驱动干细胞分化的人血清成分。在纤连蛋白上培养的 CSC 导致干细胞基因下调、分化标志物的调节以及β-连环蛋白核定位的丧失。阻断整合素 αVβ3 可抑制分化并随后抑制肿瘤形成。因此,CSC 必须通过一个或多个细胞外信号来分化并启动肿瘤形成,这为未来旨在靶向细胞外和细胞内途径的新型治疗方法定义了一个新的轴。