Evidence map›Paper›PMID 42722668›Full record

ArticleCell death discovery2026

The sperm survival switch: circRNA-mediated regulatory loops control apoptotic signalling in human spermatozoa.

Alice Luddi, Antonella Migliaccio, Matteo Prisinzano, Teresa Chioccarelli, Eugenia Annunzi, Francesca Paola Luongo, Francesca Girolamo, Maryam Raeispour, Bodo Levkau, Guillaume Martinez and 8 more

Abstract read
In one paragraph

Article in Cell death discovery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Alice Luddi *Department of Molecular Medicine and Development, University of Siena, Siena, Italy.
Antonella Migliaccio *Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Matteo PrisinzanoDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Teresa ChioccarelliDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Eugenia AnnunziDepartment of Molecular Medicine and Development, University of Siena, Siena, Italy.
Francesca Paola LuongoDepartment of Molecular Medicine and Development, University of Siena, Siena, Italy.
Francesca GirolamoDepartment of Molecular Medicine and Development, University of Siena, Siena, Italy.
Maryam RaeispourDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Bodo LevkauInstitute of Molecular Medicine III, Heinrich Heine University, Düsseldorf, Germany.ORCID http://orcid.org/0000-0002-0005-125X
Guillaume MartinezHôpital Couple-Enfant, Centre Hospitalier Universitaire de Grenoble, UM de Génétique Chromosomique, Grenoble, France.
Charles CouttonHôpital Couple-Enfant, Centre Hospitalier Universitaire de Grenoble, UM de Génétique Chromosomique, Grenoble, France.
Michele CaragliaDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.ORCID http://orcid.org/0000-0003-2408-6091
Caterina BernacchioniDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Gilda CobellisDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Chiara DonatiDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.
Francesco ManfrevolaDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy. francesco.manfrevola@unicampania.it.ORCID http://orcid.org/0000-0003-0459-7644
Rosanna ChianeseDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy. rosanna.chianese@unicampania.it.ORCID http://orcid.org/0000-0003-3631-1794
Paola PiomboniDepartment of Molecular Medicine and Development, University of Siena, Siena, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Male reproductive health is declining worldwide, partly due to lifestyle factors including obesity, which is linked to increased sperm apoptosis and impaired assisted reproductive technologies (ARTs) outcomes. This growing issue underscores the urgent need for novel molecular biomarkers capable of improving sperm quality assessment. In this context, circular RNAs (circRNAs) are emerging as regulators of germ cell functions and apoptosis, but their role as early apoptotic markers in human sperm under lifestyle-related stress remains poorly explored. In this study, by using the obesity as experimental condition of sperm apoptosis-induction, we performed a comprehensive circRNA profiling in High-quality spermatozoa (A-SPZ) collected from Normal-weight and Obese men. Obese sperm exhibit a pro-apoptotic phenotype associated with a cargo of differentially expressed (DE-) circRNAs enriched in pro-apoptotic regulatory networks. Mechanistically, circRNAs arise both from the trigger of FUS-regulated endogenous backsplicing and via extracellular vesicles (EVs) mediated delivery, thereby establishing a functional pro-apoptotic circRNA regulatory circuit. Furthermore, Obese men exhibit a dysregulated sphingosine 1-phosphate (S1P) signaling axis, along with an imbalanced S1P-to-ceramide rheostat within EVs and increased levels of pro-apoptotic ceramide. Finally, the in vitro sperm apoptosis induction confirmed a functional circRNA-apoptosis axis, identifying a subset of circRNAs responsive to pro-apoptotic stimuli that engage in a self-reinforcing regulatory loop involving pro-CASPASE3 activation. Our findings elucidate a pro-apoptotic propensity in Obese A-SPZ positioning circRNAs as putative molecular biomarkers candidate for early apoptosis. These spermatic circRNAs, which are significantly up-regulated under apoptotic conditions, exert a dual functional role: (i) serving as diagnostic markers for early-stage apoptosis and (ii) acting as active molecular adapters to enhance apoptosis activation. These circRNAs could be suggested as early sperm apoptotic biomarkers enhancing the precision of sperm quality assessment and, in turn, the success of ART procedures.

Identifiers

PMID42722668
PMCPMC13562583

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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 OpenQuestion graph.