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Minichromosome maintenance protein 7 expression in gestational trophoblastic disease: correlation with Ki67, PCNA and clinicopathological parameters
Author(s) -
Xue W C,
Khoo U S,
Ngan H Y S,
Chan K Y K,
Chiu P M,
Tsao S W,
Cheung A N Y
Publication year - 2003
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1046/j.1365-2559.2003.01728.x
Subject(s) - minichromosome maintenance , proliferating cell nuclear antigen , correlation , pathology , biology , protein expression , immunohistochemistry , disease , gestational trophoblastic disease , medicine , oncology , cancer research , pregnancy , gestation , genetics , gene , geometry , mathematics , eukaryotic dna replication
Aims: To assess the proliferative activity of gestational trophoblastic disease (GTD) using one of the novel proliferation markers (MCM7) and to determine its prognostic value in hydatidiform mole (HM). Methods and results: Immunohistochemical staining for MCM7 was performed on 122 samples of paraffin‐embedded trophoblastic tissues including 22 normal first‐trimester placentas, 12 term placentas, 12 spontaneous miscarriages (SM), 21 partial moles (PM), 44 complete hydatidiform moles (CM), and 11 choriocarcinomas (CCA). The correlations between the proliferative indices assessed by MCM7, proliferating cell nuclear antigen (PCNA) and Ki67 (MIB1) immunoreactivity as well as clinical progress were assessed. MCM7 immunoreactivity was found predominantly in the nuclei of cytotrophoblast and intermediate trophoblast and decreased with placental maturation. MCM7 expression was highest in CCA, followed by CM, PM, normal first‐trimester placenta, SM and term placenta. MCM7 index was significantly higher in PM and CM than in SM ( P = 0.007, P < 0.001) but not between PM and CM themselves ( P = 0.560). Eighteen of the 65 patients with HM developed persistent trophoblastic disease (PTD) requiring chemotherapy. There was no significant difference in MCM7 indices between the patients who developed PTD and those who did not ( P = 0.312). MCM7 indices correlated well with Ki67 ( P = 0.002) but not with PCNA ( P = 0.054) indices. MCM7 indices demonstrated less variability than PCNA and Ki67 and may be a better proliferation marker than the latter two. Conclusions: We conclude that MCM7 is useful in differentiating molar and non‐molar gestations but is not helpful in discriminating PM from CM or in predicting PTD.