A B ST R AC T Background:P120(ctn)isaspecificmembranousadhesionprotein,thatmaintainsthestabilityofintercellularjunctions.Analtered expressionofp120(ctn),eitherreducedinthecellmembraneorincreaseinthecytoplasm,playsacrucialroleincarcinogenesis.No researchhasanalysedtheexpressionofp120(ctn)inbasalcellcarcinoma(BCC)oftheskinsofar.Therefore,weimmunohistochemically studiedp120(ctn)inasetofcutaneousBCCsinordertodetermine,whetherthereisdifferenceintheexpressionpatternrelatedtothe histologicsubtypesandtumorgrowthcharacteristics.MaterialandMethods:Thestudygroupconsistedof38BCCscathegorizedinto low-risk(non-infiltrative)subroup(8superficialand12nodularsubtypes)andhigh-risk(infiltrative)subgroup(10nodular-infiltrativeand 8infiltrativesubtypes).Specificmonoclonalantibodyagainstp120(ctn)wasusedforstaining.Results:Overall,therewere12cases(31.6%) withnormalpreservedand26cases(68.4%)withabnormalp120(ctn)expression.Insuperficial,nodular,nodular-infiltrativeandinfiltrative subtypes,abnormalp120(ctn)immunoreactivitywasfoundin37.5%(3/8),41.7%(5/12),100%(10/10)and100%(8/8),respectively.We haveconfirmedastrongcorrelationbetweentheexpressionofp120(ctn)andbothgiven,non-infiltrativeandinfiltrativeBCCgrowth phenotypes.Inthelattersubgroup,almostalllesionsshoweddiffuselyreducedmembranousstaining,ofwhichfivealsomanifestedan aberrantimmunoreactivityinthecytoplasm.Thiscytoplasmicpositivityoccurredsolelyattheinvasivefrontoftheinfiltrativetumor formations.Conclusion:Ourresultsshowedthatdecreasedmembranousexpressionofp120(ctn)wasafrequenteventinhumancutaneous BCCanditwasassociatedwithinfiltrativegrowthphenotype.ConsideringthatnearlyhalfoftheBCCswithnon-infiltrativegrowthpattern alsoexhibitedreducedmembranousexpression,aberrantcytoplasmicimmunoreactivityofp120(ctn),whichwasfoundexclusivelyinthe high-riskBCCvariants,canmorereliablyreflectandpredictbiologicalbehaviourandmalignantpotential.