Evidence map›Paper›PMID 39862403›Full record

ArticleMolecular human reproduction2025

Pro-cumulin addition in a biphasic in vitro oocyte maturation system modulates human oocyte and cumulus cell transcriptomes.

Berta Cava-Cami, Antonio Galvao, Heidi Van Ranst, William A Stocker, Craig A Harrison, Johan Smitz, Michel De Vos, Gavin Kelsey, Ellen Anckaert

Abstract read
In one paragraph

Article in Molecular human reproduction, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Berta Cava-CamiFollicle Biology Laboratory, Research Group Genetics, Reproduction and Development, Vrije Universiteit Brussel (VUB), Brussels, Belgium.ORCID 0000-0002-8547-0532
Antonio GalvaoInstitute of Animal Reproduction and Food Research, Polish Academy of Science, Olsztyn, Poland.
Heidi Van RanstFollicle Biology Laboratory, Research Group Genetics, Reproduction and Development, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
William A StockerDepartment of Physiology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.ORCID 0009-0001-8334-2027
Craig A HarrisonDepartment of Physiology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.
Johan SmitzFollicle Biology Laboratory, Research Group Genetics, Reproduction and Development, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Michel De VosFollicle Biology Laboratory, Research Group Genetics, Reproduction and Development, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Gavin KelseyBabraham Institute, Epigenetics Programme, Cambridge, UK.ORCID 0000-0002-9762-5634
Ellen AnckaertFollicle Biology Laboratory, Research Group Genetics, Reproduction and Development, Vrije Universiteit Brussel (VUB), Brussels, Belgium.

Funding

European Union's Horizon 2020 Research and innovation programme 860960Medical Research Council MR/S000437/1UK Biotechnology and Biological Sciences Research Council BBS/E/B/000C0423VUB Research FundingWellcome TrustWellcome Trust 210754/B/18/Z
6 · The paper itself

Abstract

Biphasic IVM can be offered as a patient-friendly alternative to conventional ovarian stimulation in IVF patients predicted to be hyper-responsive to ovarian stimulation. However, cumulative live birth rates after IVM per cycle are lower than after conventional ovarian stimulation for IVF. In different animal species, supplementation of IVM media with oocyte-secreted factors (OSFs) improves oocyte developmental competence through the expression of pro-ovulatory genes in cumulus cells. Whether the addition of OSFs in human biphasic IVM culture impacts the transcriptome of oocytes and cumulus cells retrieved from small antral follicles in minimally stimulated non-hCG-triggered IVM cycles remains to be elucidated. To answer this, human cumulus-oocyte complexes (COCs) that were fully surrounded by cumulus cells or partially denuded at the time of retrieval were cultured in a biphasic IVM system either without or with the addition of pro-cumulin, a GDF9:BMP15 heterodimer. Oocytes and their accompanying cumulus cells were collected separately, and single-cell RNA-seq libraries were generated. The transcriptomic profile of cumulus cells revealed that pro-cumulin upregulated the expression of genes involved in cumulus cell expansion and proliferation while downregulating steroidogenesis, luteinization, and apoptosis pathways. Moreover, pro-cumulin modulated the immature oocyte transcriptome during the pre-maturation step, including regulating translation, apoptosis, and mitochondria remodeling pathways in the growing germinal vesicle oocytes. The addition of pro-cumulin also restored the transcriptomic profile of matured metaphase II oocytes that were partially denuded at collection. These results suggest that cumulus cell and oocyte transcriptome regulation by pro-cumulin may increase the number of developmentally competent oocytes after biphasic IVM treatment. Future studies should assess the effects of pro-cumulin addition in human biphasic IVM at the proteomic level and the embryological outcomes, particularly its potential to enhance outcomes of oocytes that are partially denuded at COC collection.

Indexed as

Bone Morphogenetic Protein 15Cumulus CellsGrowth Differentiation Factor 9In Vitro Oocyte Maturation TechniquesOocytesTranscriptomeAdultFemaleFertilization in VitroHumansOogenesisOvulation InductionBMP15 protein, humanBone Morphogenetic Protein 15GDF9 protein, humanGrowth Differentiation Factor 9biphasic IVMcumulus cellsoocyteoocyte-secreted factors (OSFs)pre-maturationRNA-seqsingle-cell transcriptomics

Identifiers

PMID39862403
PMCPMC11842067

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.