E-cadherin and its messenger ribonucleic acid in periimplantation phase human endometrium in normal and clomiphene-treated cycles.
basic_science · Level V
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Abstract
The purpose of this investigation was to determine whether treatment with clomiphene citrate, which is estrogenic and antiestrogenic, affects the expression of the cell adhesion molecule E-cadherin in human periimplantation phase endometrium. Five healthy women were studied for two cycles each, a control and a treated (clomiphene 50 mg daily, days 5 through 9) cycle. A biopsy specimen of endometrial tissue was studied (8 to 10 days post luteinizing hormone surge) for immunohistochemical localization, Western analysis of E-cadherin with use of a highly specific monoclonal antibody to human E-cadherin, and determination of messenger ribonucleic acid for E-cadherin by reverse transcription-polymerase chain reaction by use of oligonucleotide primers specific to E-cadherin and amplifying a 432 bp fragment. Luteal phase plasma progesterone levels were significantly higher in clomiphene cycles. E-cadherin was immunocytochemically present in endometrium of control and treated cycles with no apparent difference in staining intensity. Western blots revealed the presence of E-cadherin. It was relatively more abundant in clomiphene-treated than control cycles but not significantly different. The message for E-cadherin gene is expressed in endometrium of control (n = 5) and clomiphene cycles (n = 4). E-cadherin and its gene transcripts are expressed in periimplantation phase endometrium and are not significantly affected by clomiphene treatment.
Medical subject headings
- Adult
- Biopsy
- Blotting, Western
- Cadherins
- Cadherins/analysis
- Cadherins/genetics
- Cadherins/metabolism
- Clomiphene
- Clomiphene/pharmacology
- Embryo Implantation
- Endometrium
- Endometrium/drug effects
- Endometrium/metabolism
- Female
- Humans
- Immunohistochemistry
- Polymerase Chain Reaction
- Pregnancy
- Progesterone
- Progesterone/blood
- RNA, Messenger
- RNA, Messenger/analysis
- RNA, Messenger/metabolism
- RNA-Directed DNA Polymerase