Loss of intercellular adhesion activates a transition from low‐ to high‐grade human squamous cell carcinoma

The relationship between loss of intercellular adhesion and the biologic properties of human squamous cell carcinoma is not well understood. We investigated how abrogation of E‐cadherin‐mediated adhesion influenced the behavior and phenotype of squamous cell carcinoma in 3D human tissues. Cell‐cell adhesion was disrupted in early‐stage epithelial tumor cells (HaCaT‐II‐4) through expression of a dominant‐negative form of E‐cadherin (H‐2K d ‐Ecad). Three‐dimensional human tissue constructs harboring either H‐2K d ‐Ecad‐expressing or control II‐4 cells (pBabe, H‐2K d ‐EcadΔC25) were cultured at an air‐liquid interface for 8 days and transplanted to nude mice; tumor phenotype was analyzed 2 days and 2 and 4 weeks later. H‐2K d ‐Ecad‐expressing tumors demonstrated a switch to a high‐grade aggressive tumor phenotype characterized by poorly differentiated tumor cells that infiltrated throughout the stroma. This high‐grade carcinoma revealed elevated cell proliferation in a random pattern, loss of keratin 1 and diffuse deposition of laminin 5 γ2 chain. When II‐4 cell variants were seeded into type I collagen gels as an in vitro assay for cell migration, we found that only E‐cadherin‐deficient cells detached, migrated as single cells and expressed N‐cadherin. Function‐blocking studies demonstrated that this migration was matrix metalloproteinase‐dependent, as GM‐6001 and TIMP‐2, but not TIMP‐1, could block migration. Gene expression profiles revealed that E‐cadherin‐deficient II‐4 cells demonstrated increased expression of proteases and cell‐cell and cell‐matrix proteins. These findings showed that loss of E‐cadherin‐mediated adhesion plays a causal role in the transition from low‐ to high‐grade squamous cell carcinomas and that the absence of E‐cadherin is an important prognostic marker in the progression of this disease. © 2005 Wiley‐Liss, Inc.