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Objective:The purpose of this studywas to test whether a quantitative high-throughput molecular screen can be used to probe human endometrium and initiate the development of molecular diagnostic tools with potential for identification of therapeutic targets in women with menstrual complaints. Study design:Endometrium was collected from 10 patients with complaint of heavy bleeding,classified into mid or late secretory phase of the menstrual cycle by histologic dating and serum progesterone concentration. Total RNA was extracted and gene activity assessed using high-density oligonucleotide arrays. Results:Statistical testing identified 83 ‘signature’genes whose expression levels differentiated the mid and late secretory phases of the menstrual cycle. Conclusion:The results show that the endometrium,a complex heterogeneous tissue,is amenable to high-throughput molecular analyses and this work provides further support for the future application of molecular profiling to clinical diagnosis.
Objective: The purpose of this study was to test whether a quantitative high-throughput molecular screen can be used to probe human endometrium and start the development of molecular diagnostic tools with potential for identification of therapeutic targets in women with menstrual complaints. Study design: Endometrium was collected from 10 patients with complaint of heavy bleeding, classified into mid or late secretory phase of the menstrual cycle by histologic dating and serum progesterone concentration. Total RNA was extracted and gene activity assessed using high-density oligonucleotide arrays. ’signature’genes whose expression levels differentiated the mid and late secretory phases of the menstrual cycle. Conclusion: The results show that the endometrium, a complex heterogeneous tissue, is amenable to high-throughput molecular analyzes and this work provides further support for the future application of molecular profiling to clinical diagno sis.