T‐cadherin loss induces an invasive phenotype in human keratinocytes and squamous cell carcinoma (SCC) cells in vitro and is associated with malignant transformation of cutaneous SCC in vivo

Background  Cadherins play important roles in controlling keratinocyte growth, differentiation and survival. Atypical glycosylphosphatidylinositol‐anchored T‐cadherin (T‐cad) is highly expressed in the basal keratinocyte layer of skin. The role of T‐cad in keratinocyte biology and pathology is unclear.

[1]  P. Erne,et al.  High T‐cadherin expression is a feature of basal cell carcinoma , 2009, The British journal of dermatology.

[2]  Andrés J. García,et al.  Cadherin-mediated cell-cell contact regulates keratinocyte differentiation. , 2009, The Journal of investigative dermatology.

[3]  Suzanne M Olbricht,et al.  Cutaneous squamous cell carcinoma. , 2008, Advances in dermatology.

[4]  C. Kang,et al.  Comparative analysis of immunohistochemical markers with invasiveness and histologic differentiation in squamous cell carcinoma and basal cell carcinoma of the skin , 2008, Journal of surgical oncology.

[5]  C. Kolly,et al.  Outside-in signaling through integrins and cadherins: a central mechanism to control epidermal growth and differentiation? , 2008, The Journal of investigative dermatology.

[6]  J. Bonenkamp Squamous cell carcinoma and basal cell carcinoma of the skin , 2007 .

[7]  K. Green,et al.  Desmosomes: new perspectives on a classic. , 2007, The Journal of investigative dermatology.

[8]  Preety M. Sharma,et al.  Beyond steric hindrance: the role of adhesion signaling pathways in the pathogenesis of pemphigus. , 2007, Journal of dermatological science.

[9]  V. Wilson,et al.  In vitro culture conditions to study keratinocyte differentiation using the HaCaT cell line , 2007, Cytotechnology.

[10]  A. Utani,et al.  T‐cadherin enhances cell–matrix adhesiveness by regulating β1 integrin trafficking in cutaneous squamous carcinoma cells , 2007, Genes to cells : devoted to molecular & cellular mechanisms.

[11]  D. Piatier‐Tonneau,et al.  Expression of T‐cadherin in tumor cells influences invasive potential of human hepatocellular carcinoma , 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[12]  P. Erne,et al.  Atypical GPI-Anchored T-Cadherin Stimulates Angiogenesis In Vitro and In Vivo , 2006, Arteriosclerosis, thrombosis, and vascular biology.

[13]  D. Cassarino,et al.  Cutaneous squamous cell carcinoma: a comprehensive clinicopathologic classification , 2006, Journal of cutaneous pathology.

[14]  D. Cassarino,et al.  Cutaneous squamous cell carcinoma: a comprehensive clinicopathologic classification , 2006, Journal of cutaneous pathology.

[15]  A. Margulis,et al.  E-cadherin loss promotes the initiation of squamous cell carcinoma invasion through modulation of integrin-mediated adhesion , 2006, Journal of Cell Science.

[16]  S. Cai,et al.  Overexpression of Phosphorylated‐STAT3 Correlated with the Invasion and Metastasis of Cutaneous Squamous Cell Carcinoma , 2005, The Journal of dermatology.

[17]  Y. Miyachi,et al.  T-cadherin negatively regulates the proliferation of cutaneous squamous carcinoma cells. , 2005, The Journal of investigative dermatology.

[18]  P. Erne,et al.  RhoA and Rac mediate endothelial cell polarization and detachment induced by T‐cadherin , 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[19]  H. Trau,et al.  Expression of E-Cadherin and Beta-Catenin in Cutaneous Squamous Cell Carcinoma and its Precursors , 2004, The American Journal of dermatopathology.

[20]  Valerie J. Brown Hazardous Waste: Electronics, Lead, and Landfills , 2004, Environmental health perspectives.

[21]  B. Smoller,et al.  Metalloproteinase-2 expression correlates with aggressiveness of cutaneous squamous cell carcinomas , 2004, Modern Pathology.

[22]  G. Christofori,et al.  Multitasking in Tumor Progression: Signaling Functions of Cell Adhesion Molecules , 2004, Annals of the New York Academy of Sciences.

[23]  P. Erne,et al.  Cell adhesion molecule T-cadherin regulates vascular cell adhesion, phenotype and motility. , 2004, Experimental cell research.

[24]  N. Penneys,et al.  P27 And Mib1 Expression in Actinic Keratosis, Bowen Disease, and Squamous Cell Carcinoma , 2004, The American Journal of dermatopathology.

[25]  B. Smoller,et al.  Ets‐1 immunohistochemical expression in non‐melanoma skin carcinoma , 2004, Journal of cutaneous pathology.

[26]  H. Kurzen,et al.  Expression of desmosomal proteins in squamous cell carcinomas of the skin , 2003, Journal of cutaneous pathology.

[27]  P. Erne,et al.  Polarisation of T-cadherin to the leading edge of migrating vascular cells in vitro: a function in vascular cell motility? , 2003, Histochemistry and Cell Biology.

[28]  Y. Ohtsuki,et al.  Reciprocal altered expression of T‐cadherin and P‐cadherin in psoriasis vulgaris , 2003, The British journal of dermatology.

[29]  P. Friedl,et al.  Tumour-cell invasion and migration: diversity and escape mechanisms , 2003, Nature Reviews Cancer.

[30]  Y. Ohtsuki,et al.  Downregulation of expression of a novel cadherin molecule, T‐cadherin, in basal cell carcinoma of the skin , 2002, Molecular carcinogenesis.

[31]  Y. Ohtsuki,et al.  Loss of T-Cadherin (CDH13, H-Cadherin) Expression in Cutaneous Squamous Cell Carcinoma , 2002, Laboratory Investigation.

[32]  Y. Ohtsuki,et al.  Expression of T-cadherin in Basal keratinocytes of skin. , 2002, The Journal of investigative dermatology.

[33]  D. Czarnecki,et al.  The Majority of Cutaneous Squamous Cell Carcinomas Arise in Actinic Keratoses , 2002, Journal of cutaneous medicine and surgery.

[34]  D. Gutmann,et al.  Heterozygosity for the neurofibromatosis 1 (NF1) tumor suppressor results in abnormalities in cell attachment, spreading and motility in astrocytes. , 2001, Human molecular genetics.

[35]  P. Amerio,et al.  Cutaneous carcinomas and preinvasive neoplastic lesions. Role of MMP‐2 and MMP‐9 metalloproteinases in neoplastic invasion and their relationship with proliferative activity and p53 expression , 2001, Journal of cutaneous pathology.

[36]  Kathleen J. Green,et al.  Are desmosomes more than tethers for intermediate filaments? , 2000, Nature Reviews Molecular Cell Biology.

[37]  L. Rodriguez-Rodriguez,et al.  CD44-9v and CD44-10v Are Potential Molecular Markers for Squamous Cell Carcinoma of the Vulva , 2000, The Journal of the Society for Gynecologic Investigation: JSGI.

[38]  Y. Mitsuhashi,et al.  An Immunohistochemical Study of E‐Cadherin Expression in Human Squamous Cell Carcinoma of the Skin , 1999, The Journal of dermatology.

[39]  Z. Werb,et al.  Misregulation of Stromelysin-1 Expression in Mouse Mammary Tumor Cells Accompanies Acquisition of Stromelysin-1-dependent Invasive Properties* , 1997, The Journal of Biological Chemistry.

[40]  B. Fredette,et al.  Inhibition of motor axon growth by T-cadherin substrata. , 1996, Development.

[41]  Jensen Pj,et al.  The relationships among adhesion, stratification and differentiation in keratinocytes. , 1996 .

[42]  D. Macdonald,et al.  Expression of E‐cadherin in human epidermal non‐melanoma cutaneous tumours , 1996, The British journal of dermatology.

[43]  B. Fredette,et al.  T-cadherin expression delineates specific regions of the developing motor axon-hindlimb projection pathway , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[44]  P. Jensen,et al.  Regulation of keratinocyte intercellular junction organization and epidermal morphogenesis by E-cadherin , 1992, The Journal of cell biology.

[45]  J. Hornung,et al.  Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line , 1988, The Journal of cell biology.

[46]  Nicholas E. Timmins,et al.  Generation of multicellular tumor spheroids by the hanging-drop method. , 2007, Methods in molecular medicine.

[47]  Cdm Fletcher,et al.  World Health Organization Classification of Tumours , 2002 .

[48]  R. Glogau The risk of progression to invasive disease. , 2000, Journal of the American Academy of Dermatology.

[49]  P. Jensen,et al.  The relationships among adhesion, stratification and differentiation in keratinocytes. , 1996, Cell death and differentiation.