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Metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential

STUDY QUESTION: Is the abundance of certain biochemical compounds in human cumulus cells (CCs) related to oocyte quality? SUMMARY ANSWER: Malonate, 5-oxyproline, and erythronate were positively associated with pregnancy potential. WHAT IS KNOWN ALREADY: CCs are removed and discarded prior to ICSI, t...

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Autores principales: Martínez-Moro, Álvaro, González-Brusi, Leopoldo, Querejeta-Fernández, Ana, Padilla-Ruiz, Ester, García-Blanco, Javier, Bermejo-Álvarez, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628504/
https://www.ncbi.nlm.nih.gov/pubmed/37697661
http://dx.doi.org/10.1093/humrep/dead181
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author Martínez-Moro, Álvaro
González-Brusi, Leopoldo
Querejeta-Fernández, Ana
Padilla-Ruiz, Ester
García-Blanco, Javier
Bermejo-Álvarez, Pablo
author_facet Martínez-Moro, Álvaro
González-Brusi, Leopoldo
Querejeta-Fernández, Ana
Padilla-Ruiz, Ester
García-Blanco, Javier
Bermejo-Álvarez, Pablo
author_sort Martínez-Moro, Álvaro
collection PubMed
description STUDY QUESTION: Is the abundance of certain biochemical compounds in human cumulus cells (CCs) related to oocyte quality? SUMMARY ANSWER: Malonate, 5-oxyproline, and erythronate were positively associated with pregnancy potential. WHAT IS KNOWN ALREADY: CCs are removed and discarded prior to ICSI, thereby constituting an interesting biological material on which to perform molecular analysis aimed to predict oocyte developmental competence. Mitochondrial DNA content and transcriptional analyses in CC have been shown to provide a poor predictive value of oocyte competence, but the untargeted analysis of biochemical compounds (metabolomics) has been unexplored. STUDY DESIGN, SIZE, DURATION: CCs were obtained from three groups of cumulus–oocyte complexes (COCs) of known developmental potential: oocytes not developing to blastocyst following ICSI (Bl−); oocytes developing to blastocyst but failing to establish pregnancy following embryo transfer (P−); and oocytes developing to blastocyst able to establish a pregnancy (P+). Metabolomics analyses were performed on 12 samples per group, each sample comprising the CC recovered from a single COC. PARTICIPANTS/MATERIALS, SETTING, METHODS: Human CC samples were obtained from IVF treatments. Only unfrozen oocytes and embryos not submitted to preimplantation genetic testing were included in the analysis. Metabolomics analysis was performed by ultra-high performance liquid chromatography-tandem mass spectroscopy. MAIN RESULTS AND THE ROLE OF CHANCE: The analysis identified 98 compounds, five of which were differentially abundant (P < 0.05) between groups: asparagine, proline, and malonate were less abundant in P− compared to Bl−, malonate and 5-oxoproline were less abundant in P− group compared to P+, and erythronate was less abundant in Bl− group compared to P+. No significant association between the abundance of the compounds identified and donor age or BMI was noted. LIMITATIONS, REASONS FOR CAUTION: Data dispersion and the lack of coherence between developmental groups preclude the direct use of metabolic markers in clinical practice, where the uterine environment plays a major role in pregnancy outcome. The abundance of other compounds not detected by the analysis may be associated with oocyte competence. As donors were lean (only two with BMI > 30 kg/m(2)) and young (<34 years old), a possible effect of obesity or advanced age on the CC metabolome could not be determined. WIDER IMPLICATIONS OF THE FINDINGS: The abundance of malonate, 5-oxyproline, and erythronate in CC was significantly higher in COCs ultimately establishing pregnancy, providing clues on the pathways required for oocyte competence. The untargeted analysis uncovered the presence of compounds that were not expected in CC, such as β-citrylglutamate and the neurotransmitter N-acetyl-aspartyl-glutamate, which may play roles in chromatin remodeling and signaling, respectively. STUDY FUNDING/COMPETING INTEREST(S): Research was supported by the Industrial Doctorate Project IND2017/BIO-7748 funded by Madrid Region Government. The authors declare no competing interest. TRIAL REGISTRATION NUMBER: N/A.
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spelling pubmed-106285042023-11-08 Metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential Martínez-Moro, Álvaro González-Brusi, Leopoldo Querejeta-Fernández, Ana Padilla-Ruiz, Ester García-Blanco, Javier Bermejo-Álvarez, Pablo Hum Reprod Original Article STUDY QUESTION: Is the abundance of certain biochemical compounds in human cumulus cells (CCs) related to oocyte quality? SUMMARY ANSWER: Malonate, 5-oxyproline, and erythronate were positively associated with pregnancy potential. WHAT IS KNOWN ALREADY: CCs are removed and discarded prior to ICSI, thereby constituting an interesting biological material on which to perform molecular analysis aimed to predict oocyte developmental competence. Mitochondrial DNA content and transcriptional analyses in CC have been shown to provide a poor predictive value of oocyte competence, but the untargeted analysis of biochemical compounds (metabolomics) has been unexplored. STUDY DESIGN, SIZE, DURATION: CCs were obtained from three groups of cumulus–oocyte complexes (COCs) of known developmental potential: oocytes not developing to blastocyst following ICSI (Bl−); oocytes developing to blastocyst but failing to establish pregnancy following embryo transfer (P−); and oocytes developing to blastocyst able to establish a pregnancy (P+). Metabolomics analyses were performed on 12 samples per group, each sample comprising the CC recovered from a single COC. PARTICIPANTS/MATERIALS, SETTING, METHODS: Human CC samples were obtained from IVF treatments. Only unfrozen oocytes and embryos not submitted to preimplantation genetic testing were included in the analysis. Metabolomics analysis was performed by ultra-high performance liquid chromatography-tandem mass spectroscopy. MAIN RESULTS AND THE ROLE OF CHANCE: The analysis identified 98 compounds, five of which were differentially abundant (P < 0.05) between groups: asparagine, proline, and malonate were less abundant in P− compared to Bl−, malonate and 5-oxoproline were less abundant in P− group compared to P+, and erythronate was less abundant in Bl− group compared to P+. No significant association between the abundance of the compounds identified and donor age or BMI was noted. LIMITATIONS, REASONS FOR CAUTION: Data dispersion and the lack of coherence between developmental groups preclude the direct use of metabolic markers in clinical practice, where the uterine environment plays a major role in pregnancy outcome. The abundance of other compounds not detected by the analysis may be associated with oocyte competence. As donors were lean (only two with BMI > 30 kg/m(2)) and young (<34 years old), a possible effect of obesity or advanced age on the CC metabolome could not be determined. WIDER IMPLICATIONS OF THE FINDINGS: The abundance of malonate, 5-oxyproline, and erythronate in CC was significantly higher in COCs ultimately establishing pregnancy, providing clues on the pathways required for oocyte competence. The untargeted analysis uncovered the presence of compounds that were not expected in CC, such as β-citrylglutamate and the neurotransmitter N-acetyl-aspartyl-glutamate, which may play roles in chromatin remodeling and signaling, respectively. STUDY FUNDING/COMPETING INTEREST(S): Research was supported by the Industrial Doctorate Project IND2017/BIO-7748 funded by Madrid Region Government. The authors declare no competing interest. TRIAL REGISTRATION NUMBER: N/A. Oxford University Press 2023-09-11 /pmc/articles/PMC10628504/ /pubmed/37697661 http://dx.doi.org/10.1093/humrep/dead181 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Martínez-Moro, Álvaro
González-Brusi, Leopoldo
Querejeta-Fernández, Ana
Padilla-Ruiz, Ester
García-Blanco, Javier
Bermejo-Álvarez, Pablo
Metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential
title Metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential
title_full Metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential
title_fullStr Metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential
title_full_unstemmed Metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential
title_short Metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential
title_sort metabolomics analysis of human cumulus cells obtained from cumulus–oocyte complexes with different developmental potential
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628504/
https://www.ncbi.nlm.nih.gov/pubmed/37697661
http://dx.doi.org/10.1093/humrep/dead181
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