Evidence map›Paper›PMID 41183425›Full record

ArticleEBioMedicine2025

Characterisation of phosphate transport in epididymis and prostate with possible relevance for semen quality.

Zhihui Cui, Sam Kafai Yahyavi, Ida Marie Boisen, Lasse Bøllehuus Hansen, Niels Jørgensen, Beate Lanske, Anders Juul, Mikkel Fode, Peter Busch Østergren, Thomas Hasselager and 2 more

Abstract read
In one paragraph

Article in EBioMedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Zhihui CuiDivision of Translational Endocrinology, Department of Endocrinology and Internal Medicine, Copenhagen University Hospital - Herlev and Gentofte Hospital, Herlev, Denmark.
Sam Kafai YahyaviDivision of Translational Endocrinology, Department of Endocrinology and Internal Medicine, Copenhagen University Hospital - Herlev and Gentofte Hospital, Herlev, Denmark; Department of Growth and Reproduction and International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Ida Marie BoisenDivision of Translational Endocrinology, Department of Endocrinology and Internal Medicine, Copenhagen University Hospital - Herlev and Gentofte Hospital, Herlev, Denmark; Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.
Lasse Bøllehuus HansenDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.
Niels JørgensenDepartment of Growth and Reproduction and International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Beate LanskeDivision of Bone and Mineral Research, HSDM/HMS, Harvard University, Boston, USA.
Anders JuulDepartment of Growth and Reproduction and International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Mikkel FodeDepartment of Urology, Copenhagen University Hospital- Herlev and Gentofte Hospital, Herlev, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Peter Busch ØstergrenDepartment of Urology, Copenhagen University Hospital- Herlev and Gentofte Hospital, Herlev, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Thomas HasselagerDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Pathology, Copenhagen University Hospital - Herlev and Gentofte Hospital, Herlev, Denmark.
Anne JørgensenDivision of Translational Endocrinology, Department of Endocrinology and Internal Medicine, Copenhagen University Hospital - Herlev and Gentofte Hospital, Herlev, Denmark.
Martin Blomberg JensenDivision of Translational Endocrinology, Department of Endocrinology and Internal Medicine, Copenhagen University Hospital - Herlev and Gentofte Hospital, Herlev, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. Electronic address: martin.blomberg.jensen@regionh.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeminal phosphate concentrations are markedly higher than serum levels, suggesting a yet uncharacterised role of phosphate transporters in the male reproductive tract.

methodsAnalysis of type II and III phosphate co-transporter (SLC34A1-3/NPT2a-c, SLC20A1-2/PIT1-2) expression was conducted in prostate, seminal vesicle, and epididymis from wildtype mice fed normal or high-phosphate diet, mice treated with a NPT2a-inhibitor, Global Fgf23 knockout mice, and in human tissues. Seminal phosphate concentrations and semen quality were examined in 301 healthy men.

findingsPhosphate transporters are expressed in a zone-specific manner in the mouse epididymis and prostate. Elevated serum phosphate increased the expression of Slc34a1 (466 ± 24 vs. 1 ± 0.3, p < 0.05), Slc34a2 (54 ± 26 vs. 1 ± 0.2, p < 0.05), Slc34a3 (5 ± 0.3 vs. 1 ± 0.8, p < 0.001) and Slc20a1 (37 ± 18 vs. 1 ± 0.3, p < 0.05) to maintain a stable epididymal phosphate concentration. In contrast, prostatic phosphate concentrations increased (6.0 ± 0.4 vs. 4.5 ± 0.4, p < 0.05) with no change in expression of phosphate transporters except for lower Slc34a3 (0.1 ± 0.04 vs. 1 ± 0.4, p < 0.05). Hyperphosphatemic Fgf23 knockout mice had higher Slc20a2 expression (5.1 ± 1.1 vs. 1 ± 0.4, p < 0.05), while inhibition of NPT2a reduced phosphate concentrations specifically in caput epididymis (15 ± 0.1 vs. 19 ± 0.7, p < 0.001). Human epididymis, prostate and seminal vesicle showed distinct region-specific expression of phosphate-transporters with an abundant SLC34A2 expression in seminal vesicle. In healthy men, high seminal phosphate was positively linked with sperm concentration, motile sperm count, morphologically normal sperm (all, p < 0.05) and serum testosterone (p < 0.01).

interpretationThis study shows distinct expression and regulation of phosphate transporters in the epididymis, prostate and seminal vesicle. Moreover, both systemic and local phosphate concentrations may be of importance for reproductive organ function and semen quality.

fundingThis study was supported by funding from the Novo Nordisk Foundation, Denmark; Independent Research Fund Denmark, Denmark; Cleveland Foundation, UK; Beckett-Fonden, Denmark; Brødrene Hartmanns Fond, Denmark; Innovation Fund Denmark, Denmark.

Indexed as

EpididymisPhosphatesProstateSemen AnalysisAdultAnimalsBiological TransportFibroblast Growth Factor-23Fibroblast Growth FactorsHumansMaleMiceMice, KnockoutMiddle AgedSemenFGF23 protein, humanFgf23 protein, mouseFibroblast Growth Factor-23Fibroblast Growth FactorsPhosphatesEpididymisPhosphate transportersProstateSemen quality

Identifiers

PMID41183425
PMCPMC12677103

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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.