Identification of Vitronectin as an Extrinsic Inducer of Cancer Stem Cell Differentiation and Tumor Formation

被引:60
作者
Hurt, Elaine M. [1 ]
Chan, King [2 ]
Duhagon Serrat, Maria Ana [1 ,4 ]
Thomas, Suneetha B. [3 ]
Veenstra, Timothy D. [2 ]
Farrar, William L. [1 ]
机构
[1] NCI, Canc Stem Cell Sect, Lab Canc Prevent, Ctr Canc Res, Frederick, MD 21701 USA
[2] NCI, Lab Prote & Analyt Technol, Frederick, MD 21701 USA
[3] NCI, Basic Res Program, Sci Applicat Int Corp Frederick, Ctr Canc Res, Frederick, MD 21701 USA
[4] Univ Republica, LIM F Ciencias, Montevideo, Uruguay
关键词
Prostate cancer; Breast cancer; Tumor-initiating; Vitronectin; Arginine-glycine-aspartic acid peptide; Integrin alphaVbeta3; ACUTE MYELOID-LEUKEMIA; FOCAL-ADHESION KINASE; BREAST-CANCER; SELF-RENEWAL; IN-VITRO; STEM/PROGENITOR CELLS; INITIATING CELLS; INTEGRINS; MAINTENANCE; EXPRESSION;
D O I
10.1002/stem.271
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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. STEM CELLS 2010; 28: 390-398
引用
收藏
页码:390 / 398
页数:9
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