|
2010, Volume 26, Number 1, Page(s) 031-037
|
|
DOI: 10.5146/tjpath.2010.00992 |
Expression of Ki-67, Bcl-2 and Bax in the First Trimester Abortion Materials |
Canan KELTEN1, Osman ZEKİOĞLU2, Coşan TEREK3, Necmettin ÖZDEMİR2, Ender DÜZCAN1 |
1Department of Pathology, Pamukkale University, Faculty of Medicine, DENIZLI, TURKEY 2Ege University, Faculty of Medicine, IZMIR TURKEY 3Department of Gynecology and Obstetrics, Ege University, Faculty of Medicine, IZMIR, TURKEY |
Keywords:
Abortion, Cell proliferation, Apoptosis, Ki-67, Bcl-2, Bax |
Objective: The aim of this study was to investigate possible similar
or different mechanisms in recurrent and spontaneous abortion by
evaluating immunohistochemical correlation between proliferation
marker Ki-67, and apoptosis markers Bcl-2 and Bax in the fetal
trophoblasts and maternal deciduas from abortion material.
Material and Method: Eighty samples of curettage materials from
65 abortion patients histopathologically diagnosed “decidua showing
Arias-Stella reaction and chorionic villi” or only “decidua showing
Arias-Stella reaction” were included in the study. Hematoxylin&Eosin
stained sections from all cases were re-evaluated and further stained
immunohistochemically using antibodies against Ki-67, Bcl-2 and
Bax.
Results: Proliferation rate evaluated by Ki-67 expression both
in the cytotrophoblastic cells and decidua was found to be
significantly lower in spontaneous and recurrent abortions
compared to evacuation abortion. The extent of Bcl-2 expression in
syncytiotrophoblastic cells covering villous stroma was also decreased
in spontaneous abortion. There were no significant differences
between spontaneous and recurrent abortions in terms of Bcl-2
expression in syncytiotrophoblasts and Ki-67 proliferation index
in cytotrophoblastic cells or decidua. Bax staining showed minimal
decidual expression in a few spontaneous and recurrent abortions.
Conclusion: We concluded that proliferation rate was decreased in
fetal villous cytotrophoblasts and maternal deciduas in spontaneous
and recurrent abortions. We also proposed that loss of Bcl-2
expression in syncytiotrophoblasts may cause abortion in a subset of
cases. However, the data from spontaneous and recurrent abortions
did not not support the presence of different mechanisms in both
groups.
|
|
|
|