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Gynecol Oncol ; 104(2): 451-4, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17027071

ABSTRACT

INTRODUCTION: There is scant information about the expression of CD44 and E-cadherin, two cell adhesion molecules, and the antimetastatic protein nm23-H1, in complete hydatidiform moles. We measured the expression of these markers to determine their usefulness in predicting the development of invasive disease. MATERIALS AND METHODS: We performed a retrospective study of 27 patients with complete hydatidiform moles, collecting clinical information including the patient's age, pre-evacuation hCG level, pathology, hCG monitoring, and the development of gestational trophoblastic neoplasia. Immunohistochemical staining for CD44, E-cadherin, and nm23-H1 was performed. CD44 expression was classified as positive or negative. For E-cadherin and nm23-H1, the intensity of expression was graded on a 0 to 3 scale. Chi-square or Fisher's exact testing was used to evaluate the relationship between these markers and the development of invasive disease. RESULTS: CD44 was expressed in 26% of cases. E-cadherin expression was 1+, 2+, and 3+in 8%, 33%, and 59% of cases, respectively. Nm23-H1 expression was 1+, 2+, and 3+in 4%, 11%, and 85% of cases. The risk of developing invasive disease did not correlate with the expression of CD44, E-cadherin, or nm23-H1. CONCLUSION: In this preliminary study, there is no relationship between CD44, E-cadherin, and nm23-H1 expression in complete hydatidiform moles and the risk of invasive disease. Other molecular markers predictive of invasive disease should be sought to limit hCG surveillance to those at risk.


Subject(s)
Cadherins/biosynthesis , Hyaluronan Receptors/biosynthesis , Hydatidiform Mole/metabolism , Nucleoside-Diphosphate Kinase/biosynthesis , Uterine Neoplasms/metabolism , Adolescent , Adult , Biomarkers, Tumor/biosynthesis , Female , Humans , Hydatidiform Mole/pathology , NM23 Nucleoside Diphosphate Kinases , Neoplasm Invasiveness , Pregnancy , Retrospective Studies , Uterine Neoplasms/pathology
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