Infertility researchers identify one gene’s critical role in the human embryo implantation process

October 2005

Researchers at Cedars-Sinai Medical Center and the University of California at Los Angeles recently conducted a study of the molecular mechanism involved in the human implantation process, specifically targeting the role of one gene in the success of an embryo to implant itself in the endometrium, the inner lining of the uterus.

“There have been studies done both in the United States and Europe showing statistically that there is a defect in the implantation process in women with endometriosis, a condition affecting many premenopausal women who also suffer from infertility,” explains Lee-Chuan Kao, MD, PhD, a reproductive medicine specialist at Cedars-Sinai and co-director of the hospital’s Center for Reproductive Medicine. “My interest was to determine exactly the molecular mechanism responsible for implantation failure.”

In this recent study, Kao, working with Margareta Pisarska, MD, co-director of Cedars-Sinai’s Center for Reproductive Medicine, and Salma Khan, PhD, also of Cedars-Sinai, focused on one specific endometrial target gene (GlcNAc-6-OST) which has a role in shaping L-selectin ligand, a chemical responsible for the tethering and rolling mechanism described at the human maternal-fetal interface, ie. a signal that enables the embryo to recognize the lining of the endometrium.

“This gene (GlcNAc-6-OST) gets transcribed and then translated into a protein and this particular protein functions as an enzyme,” explains Kao. “It has been shown to be expressed specifically during the window of implantation. My hypothesis is that this particular gene, for a yet-to-be-uncovered reason, is abnormally expressed in women with endometriosis which results in the embryo not being able to find the appropriate place to bind to the endometrium leading to a failure or defect in the implantation process.”

The in-vitro study tested whether ovarian hormones, oestrogen and progesterone, can regulate the expression of GlcNAc-6-OST. By treating an endometrial cell line with the ovarian hormones, Kao and his colleagues demonstrated that increasing oestrogen during the first part of the menstrual cycle, when ovarian follicles mature to prepare for ovulation, increases the expression of the enzyme. After ovulation, progesterone production further heightens the expression of the enzyme. This up-regulation of the enzyme (when both oestrogen and progesterone are present) facilitates the production of L-selectin ligand which enables implantation. When only progesterone was present without estrogen, the gene was suppressed and the endometrium would not be receptive to implantation.

“Our next step,” says Kao, “will be to explore other regulatory mechanisms or other chemicals – instead of hormones – that might provide us with a more specific approach to modulate this gene. Additional studies are required before we can apply this information to a clinical situation but I believe we’ve shown there is definitely a need for more research.”


This study was presented at the Conjoint Annual Meeting of the American Society for Reproductive Medicine and the Canadian Fertility and Andrology Society 15-19 October 2005, in Montreal, Quebec, Canada.

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