β1 and β4 integrins: from breast development to clinical practice. Review uri icon

Overview

abstract

  • Following a highly dynamic and complex dialogue between the epithelium and the surrounding microenvironment, the mammary gland develops into a branching structure during puberty, buds during pregnancy, forms intricate polar acini during lactation and, once the babies are weaned, remodels and involutes. At every stage of menstrual and pregnancy cycles, interactions between the cells and the extracellular matrix (ECM) and homotypic and heterotypic cell–cell interactions give rise to the architecture and function of the gland at that junction. These orchestrated programs would not be possible without the important role of the ECM receptors, integrins being the prime examples. The ECM–integrin axis regulates many crucial cellular functions including survival, migration and quiescence; the imbalance in any of these processes could contribute to oncogenesis. In this review we spotlight the involvement of two prominent integrin subunits, β1 and β4 integrins, in cross-talk with tyrosine kinase receptors, and we discuss the roles of these integrin subunits in the biology of normal breast differentiation and as potential prognostic and therapeutic targets in breast cancer.

publication date

  • January 1, 2014

Research

keywords

  • Breast Neoplasms
  • Integrin beta1
  • Integrin beta4
  • Mammary Glands, Human

Identity

PubMed Central ID

  • PMC4384274

Scopus Document Identifier

  • 85047286136

Digital Object Identifier (DOI)

  • 10.1155/2012/967347

PubMed ID

  • 25606594

Additional Document Info

volume

  • 16

issue

  • 5