Brennan Kieran, Offiah Gozie, McSherry Elaine A, Hopkins Ann M
Department of Surgery, Royal College of Surgeons in Ireland, Dublin, Ireland.
J Biomed Biotechnol. 2010;2010:460607. doi: 10.1155/2010/460607. Epub 2009 Nov 15.
Breast cancer is a complex and heterogeneous disease that arises from epithelial cells lining the breast ducts and lobules. Correct adhesion between adjacent epithelial cells is important in determining the normal structure and function of epithelial tissues, and there is accumulating evidence that dysregulated cell-cell adhesion is associated with many cancers. This review will focus on one cell-cell adhesion complex, the tight junction (TJ), and summarize recent evidence that TJs may participate in breast cancer development or progression. We will first outline the protein composition of TJs and discuss the functions of the TJ complex. Secondly we will examine how alterations in these functions might facilitate breast cancer initiation or progression; by focussing on the regulatory influence of TJs on cell polarity, cell fate and cell migration. Finally we will outline how pharmacological targeting of TJ proteins may be useful in limiting breast cancer progression. Overall we hope to illustrate that the relationship between TJ alterations and breast cancer is a complex one; but that this area offers promise in uncovering fundamental mechanisms linked to breast cancer progression.
乳腺癌是一种复杂的异质性疾病,起源于乳腺导管和小叶内衬的上皮细胞。相邻上皮细胞之间的正确黏附对于确定上皮组织的正常结构和功能很重要,并且越来越多的证据表明细胞间黏附失调与许多癌症有关。本综述将聚焦于一种细胞间黏附复合体——紧密连接(TJ),并总结最近关于紧密连接可能参与乳腺癌发生或进展的证据。我们将首先概述紧密连接的蛋白质组成,并讨论紧密连接复合体的功能。其次,我们将研究这些功能的改变如何促进乳腺癌的起始或进展;重点关注紧密连接对细胞极性、细胞命运和细胞迁移的调节影响。最后,我们将概述对紧密连接蛋白进行药物靶向作用如何有助于限制乳腺癌的进展。总体而言,我们希望说明紧密连接改变与乳腺癌之间的关系是复杂的;但这一领域有望揭示与乳腺癌进展相关的基本机制。