6533b834fe1ef96bd129e021

RESEARCH PRODUCT

Abnormal Immunoexpression of Cell Adhesion Molecules (CAMs) in Cervical Cancer

Morelva Toro De MéndezAntonio Llombart Bosch

subject

AdultPathologymedicine.medical_specialtyUterine Cervical NeoplasmsAdenocarcinomaAlphapapillomavirusBiologyPathology and Forensic MedicineImmunoenzyme TechniquesBiopsyBiomarkers TumormedicineHumansDNA Probes HPVCell adhesionAgedCervical cancermedicine.diagnostic_testCadherinCell adhesion moleculeCD44v3Papillomavirus InfectionsE-cadherinCancerArtículosMiddle AgedFacultad de Farmacia y BioanálisisCadherinsmedicine.diseaseImmunohistochemistryHyaluronan ReceptorsTissue Array AnalysisDNA ViralCervical cancerCD44sImmunohistochemistryFemaleSurgeryAnatomyImmunostaining

description

Artículo publicado en: International Journal of Surgical Pathology published online 18 July 2010 The purpose of this study was to examine the immunoexpression of cell adhesion molecules (CAMs) E-cadherin, CD44s, and CD44v3 in cervical cancer and compare it with that in benign exo-endocervical tissue. In all, 81 cervical cancer biopsy specimens and 22 benign controls were included. Primary monoclonal antibodies NHC-38, F10-44-2, and 3G5 for E-cadherin, CD44s, and CD44v3 were used, respectively. Statistical significance was evaluated by the ?2 test. Antigen expression was significantly different in cervical cancer specimens compared with controls, showing marked decrease in membrane expression: E-cadherin, 6.5% and 77.3% (P < .000); CD44s, 3.9% and 81.8% (P < .000); and CD44v3, 0% and 81.8% (P < .000), respectively. The immunoexpression was significantly heterogeneous in carcinomas (P < .034) and adenocarcinomas (P < .000) for E-cadherin and CD44s. For CD44v3, no case of cancer showed immunostaining in membranes. These findings reaffirm that cell adhesion is markedly altered in cervical cancer. The authors suggest that these proteins could serve as markers for invasive cervical neoplasia. tmorelva@ula.ve antonio.llombart@uv.es

https://doi.org/10.1177/1066896909343435