Evidence map›Paper›PMID 42979254›Full record

ReviewFrontiers in endocrinology2026

The insulin gene in humans and mice: evolution, regulation, and sex-specific mechanisms of diabetes susceptibility.

Ali Mazloum, Nikita Batashkov, Veronika Ledyaeva, Gava Khulkhachiev, Dmitry Tabakov, Olga N Mityaeva, Pavel Yu Volchkov

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 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
–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

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

7 authors.

Ali MazloumMoscow Center for Advanced Studies, Moscow, Russia.
Nikita BatashkovMoscow Center for Advanced Studies, Moscow, Russia.
Veronika LedyaevaMoscow Center for Advanced Studies, Moscow, Russia.
Gava KhulkhachievFederal Research Center for Innovator and Emerging Biomedical and Pharmaceutical Technologies, Moscow, Russia.
Dmitry TabakovMoscow Center for Advanced Studies, Moscow, Russia.
Olga N MityaevaMoscow Center for Advanced Studies, Moscow, Russia.
Pavel Yu VolchkovMoscow Center for Advanced Studies, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The insulin gene (INS) encodes a peptide hormone critical for glucose homeostasis, and its dysregulation underlies both type 1 and type 2 diabetes mellitus. This review compares the structural organization and functional regulation of the insulin gene in humans and mice, highlighting key species differences including the presence of two non-allelic insulin genes (Ins1 and Ins2) in mice versus a single INS gene in humans. Despite these differences, most preclinical diabetes research has historically been conducted in male mice, potentially concealing sex and species specific mechanisms. Additionally, this review examines the growing evidence for sex-specific differences in diabetes susceptibility. Recent single-cell multi-omics studies reveal that human pancreatic islets exhibit sex-specific chromatin accessibility and gene expression patterns, with autosomal sex differences emerging predominantly in type 2 diabetes. The protective effects of estrogen, mediated through estrogen receptor α signaling, contribute to enhanced insulin sensitivity and beta-cell function in premenopausal females. We argue that routine inclusion of both sexes and species aware interpretation of insulin gene studies are prerequisites for precision diabetology.

Indexed as

Diabetes MellitusDiabetes Mellitus, Type 2Genetic Predisposition to DiseaseInsulinAnimalsFemaleGene Expression RegulationHumansMaleMiceSex CharacteristicsInsulinbeta-cell biologycomparative genomicsdiabetes mellitusinsulin gene (INS)insulin regulationmouse modelsprecision medicinesex differences

Identifiers

PMID42979254
PMCPMC13728926

What OpenQuestion holds

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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 OpenQuestion graph.