Evidence map›Paper›PMID 40336300›Full record

ArticleEndocrinology2025

Functional Analysis of HSD17B3-Deficient Male Mice Reveals Roles for HSD17B7 and HSD17B12 in Testosterone Biosynthesis.

Ben M Lawrence, Liza O'Donnell, Anne-Louise Gannon, David A Skerrett-Byrne, Shanmathi Parameswaran, Imogen Abbott, Sarah Smith, David J Handelsman, Diane Rebourcet, Lee B Smith

Abstract read
In one paragraph

Article in Endocrinology, 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

10 authors.

Ben M LawrenceCollege of Engineering, Science and Environment, The University of Newcastle, Callaghan, New South Wales 2308, Australia.ORCID 0000-0002-7803-1611
Liza O'DonnellOffice of the Deputy Vice-Chancellor (Research), Griffith University, Southport, Queensland 4222, Australia.ORCID 0000-0001-5848-6136
Anne-Louise GannonCollege of Engineering, Science and Environment, The University of Newcastle, Callaghan, New South Wales 2308, Australia.ORCID 0000-0001-6137-4063
David A Skerrett-ByrneCollege of Engineering, Science and Environment, The University of Newcastle, Callaghan, New South Wales 2308, Australia.ORCID 0000-0002-1804-1826
Shanmathi ParameswaranCollege of Engineering, Science and Environment, The University of Newcastle, Callaghan, New South Wales 2308, Australia.
Imogen AbbottCollege of Engineering, Science and Environment, The University of Newcastle, Callaghan, New South Wales 2308, Australia.
Sarah SmithCollege of Engineering, Science and Environment, The University of Newcastle, Callaghan, New South Wales 2308, Australia.
David J HandelsmanUniversity of Sydney and Andrology Department, ANZAC Research Institute, Concord Hospital, Sydney, New South Wales 2139, Australia.ORCID 0000-0002-4200-7476
Diane RebourcetCollege of Engineering, Science and Environment, The University of Newcastle, Callaghan, New South Wales 2308, Australia.
Lee B SmithOffice of the Deputy Vice-Chancellor (Research), Griffith University, Southport, Queensland 4222, Australia.ORCID 0000-0002-4103-3074

Funding

Griffith UniversityNational Health and Medical Research Council APP1158344
6 · The paper itself

Abstract

Historically, 17β-hydroxysteroid dehydrogenase type 3 (HSD17B3) was thought to be the key enzyme responsible for testicular testosterone production. In humans, loss-of-function mutations in HSD17B3 impair testosterone production during prenatal life leading to impaired development of androgen-dependent tissues in 46,XY individuals. However, male mice with HSD17B3 deficiency exhibit normal testicular testosterone concentrations, normal development of reproductive organs and are fertile, suggesting that mice express other hydroxysteroid dehydrogenase enzymes capable of testicular testosterone synthesis. This study aimed to investigate whether 17β-hydroxysteroid dehydrogenase type 12 (HSD17B12), which can convert androstenedione to testosterone in mice but not in humans, compensates for the lack of HSD17B3 in Hsd17b3 knockout (KO) mice. We used CRISPR/Cas9 to substitute the amino acid in mouse HSD17B12 that is responsible for its ability to convert androstenedione to testosterone with the amino acid of the human enzyme that prevents androstenedione being used as a substrate. When this Hsd17b12 mutation was introduced into Hsd17b3 KO mice, males exhibited normal reproductive tracts but reduced testicular testosterone production with a consequential reduction in seminal vesicle weight. This suggests HSD17B12 contributes toward testosterone production in the absence of HSD17B3, but other enzymes must also contribute. We therefore quantified other testicular hydroxysteroid dehydrogenases, finding that HSD17B7 mRNA and protein was markedly upregulated in Hsd17b3 KO testes. We confirmed that mouse, but not human, HSD17B7 can produce testosterone in vitro. We conclude that compared to humans, mice exhibit increased plasticity in testosterone production via hydroxysteroid dehydrogenase enzymes to support androgen action and male fertility.

Indexed as

17-Hydroxysteroid DehydrogenasesTestosteroneAndrostenedioneAnimalsHumansMaleMiceMice, KnockoutTestis17beta-hydroxysteroid dehydrogenase type 317-Hydroxysteroid DehydrogenasesAndrostenedioneTestosteroneandrogenshydroxysteroid dehydrogenasemale fertilitytestistestosterone

Identifiers

PMID40336300
PMCPMC12059215

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.