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Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure

Background: Homeobox genes A10 (HOXA10) and A11 (HOXA11), members of the abdominal B gene family, are responsible for embryonic survival and implantation. This study was planned to investigate whether endometrial injury alters the expression of both transcripts in women with implantation failure. Me...

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Autores principales: Celik, Onder, Yurci, Arzu, Ersahin, Aynur, Gungor, Nur D., Celik, Nilufer, Ozcil, Mustafa D., Dogan, Serdar, Dalkilic, Semih, Dalkilic, Lutfiye, Ulug, Ulun, Celik, Sudenaz, Tinelli, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002420/
https://www.ncbi.nlm.nih.gov/pubmed/36900953
http://dx.doi.org/10.3390/ijerph20053942
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author Celik, Onder
Yurci, Arzu
Ersahin, Aynur
Gungor, Nur D.
Celik, Nilufer
Ozcil, Mustafa D.
Dogan, Serdar
Dalkilic, Semih
Dalkilic, Lutfiye
Ulug, Ulun
Celik, Sudenaz
Tinelli, Andrea
author_facet Celik, Onder
Yurci, Arzu
Ersahin, Aynur
Gungor, Nur D.
Celik, Nilufer
Ozcil, Mustafa D.
Dogan, Serdar
Dalkilic, Semih
Dalkilic, Lutfiye
Ulug, Ulun
Celik, Sudenaz
Tinelli, Andrea
author_sort Celik, Onder
collection PubMed
description Background: Homeobox genes A10 (HOXA10) and A11 (HOXA11), members of the abdominal B gene family, are responsible for embryonic survival and implantation. This study was planned to investigate whether endometrial injury alters the expression of both transcripts in women with implantation failure. Methods: A total of 54 women with implantation failure were divided into two equal groups as experimental (scratching) and sham (no scratching). Participants in the scratching group were exposed to endometrial injury in the mid-luteal phase, and those in the sham group were exposed to endometrial flushing. The scratching group, but not the sham group, underwent prior endometrial sampling. A second endometrial sampling was performed on the scratching group in the mid-luteal phase of the following cycle. The mRNA and protein levels of the HOXA10 and 11 transcripts were determined in endometrial samples collected before and after injury/flushing. Participants in each group underwent IVF/ET in the cycle after the second endometrial sampling. Results: Endometrial injury caused a 60.1-fold (p < 0.01) increase in HOXA10 mRNA and a 9.0-fold increase in HOXA11 mRNA (p < 0.02). Injury resulted in a significant increase in both HOXA10 (p < 0.001) and HOXA11 protein expression (p < 0.003). There was no significant change in HOXA10 and 11 mRNA expressions after flushing. Clinical pregnancy, live birth, and miscarriage rates of the both groups were similar. Conclusions: Endometrial injury increases homeobox transcript expression at both mRNA and protein levels.
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spelling pubmed-100024202023-03-11 Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure Celik, Onder Yurci, Arzu Ersahin, Aynur Gungor, Nur D. Celik, Nilufer Ozcil, Mustafa D. Dogan, Serdar Dalkilic, Semih Dalkilic, Lutfiye Ulug, Ulun Celik, Sudenaz Tinelli, Andrea Int J Environ Res Public Health Article Background: Homeobox genes A10 (HOXA10) and A11 (HOXA11), members of the abdominal B gene family, are responsible for embryonic survival and implantation. This study was planned to investigate whether endometrial injury alters the expression of both transcripts in women with implantation failure. Methods: A total of 54 women with implantation failure were divided into two equal groups as experimental (scratching) and sham (no scratching). Participants in the scratching group were exposed to endometrial injury in the mid-luteal phase, and those in the sham group were exposed to endometrial flushing. The scratching group, but not the sham group, underwent prior endometrial sampling. A second endometrial sampling was performed on the scratching group in the mid-luteal phase of the following cycle. The mRNA and protein levels of the HOXA10 and 11 transcripts were determined in endometrial samples collected before and after injury/flushing. Participants in each group underwent IVF/ET in the cycle after the second endometrial sampling. Results: Endometrial injury caused a 60.1-fold (p < 0.01) increase in HOXA10 mRNA and a 9.0-fold increase in HOXA11 mRNA (p < 0.02). Injury resulted in a significant increase in both HOXA10 (p < 0.001) and HOXA11 protein expression (p < 0.003). There was no significant change in HOXA10 and 11 mRNA expressions after flushing. Clinical pregnancy, live birth, and miscarriage rates of the both groups were similar. Conclusions: Endometrial injury increases homeobox transcript expression at both mRNA and protein levels. MDPI 2023-02-23 /pmc/articles/PMC10002420/ /pubmed/36900953 http://dx.doi.org/10.3390/ijerph20053942 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Celik, Onder
Yurci, Arzu
Ersahin, Aynur
Gungor, Nur D.
Celik, Nilufer
Ozcil, Mustafa D.
Dogan, Serdar
Dalkilic, Semih
Dalkilic, Lutfiye
Ulug, Ulun
Celik, Sudenaz
Tinelli, Andrea
Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure
title Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure
title_full Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure
title_fullStr Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure
title_full_unstemmed Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure
title_short Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure
title_sort endometrial injury upregulates expression of receptivity genes in women with implantation failure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002420/
https://www.ncbi.nlm.nih.gov/pubmed/36900953
http://dx.doi.org/10.3390/ijerph20053942
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