In search of candidate genes critically expressed in the human endometrium during the window of implantation

• Published in: Human reproduction (Oxford) Vol. 20; no. 8; pp. 2104 - 2117
• Main Authors: Mirkin, S., Arslan, M., Churikov, D., Corica, A., Diaz, J.I., Williams, S., Bocca, S., Oehninger, S.
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.08.2005; Oxford Publishing Limited (England)
• Subjects: Adult; Biological and medical sciences; Computational Biology; Embryo Implantation - genetics; endometrium; Endometrium - physiology; Female; gene expression; Gene Expression Profiling; Gynecology. Andrology. Obstetrics; Humans; implantation; luteal phase; Medical sciences; microarray; Oligonucleotide Array Sequence Analysis; Pregnancy; Promoter Regions, Genetic - genetics; Prospective Studies; Receptors, Estrogen - genetics; Receptors, Progesterone - genetics; Reverse Transcriptase Polymerase Chain Reaction; endometrium; implantation; microarray; gene expression; luteal phase; Pregnancy; Human; Vertebrata; Luteal phase; Mammalia; endometrium/gene expression/implantation/luteal phase/microarray; Uterus; Ovum implantation; Female genital system; Candidate gene; Gene expression; Endometrium
• ISSN: 0268-1161; 1460-2350
• DOI: 10.1093/humrep/dei051

BACKGROUND: In this prospective randomized blinded clinical trial, we examined gene expression profiles of the human endometrium during the early and mid-luteal phases of the natural cycle. METHODS: An endometrial biopsy was performed on day 16 (LH +3) or on day 21 (LH +8), followed by RNA extraction and microarray analysis using an Affymetrix HG-U95A microchip. Data analysis was carried out using pairwise multiple group comparison with the significance analysis of microarrays (SAM) software. RESULTS: With a false discovery rate of 0, the analysis revealed that 107 genes were significantly and differently expressed (≥2-fold) during the early versus the mid-luteal phase of the cycle. Forty-five of these genes have not been previously linked to endometrial receptivity. Validation of the microarray data was accomplished using semiquantitative RT–PCR. We demonstrated the presence of estrogen and progesterone response elements (ERE and PRE) by analysis of the 5′-flanking regions of a subset of differentially regulated genes. CONCLUSIONS: Using a strict bioinformatics approach of microarray data, we demonstrated significant changes in candidate genes during the transition of the early to the mid-luteal phase of the human endometrium that may have functional significance for the opening and maintenance of the window of implantation.