Evidence map›Paper›PMID 39546465›Full record

ArticlePloS one2024

The mouse gingiva and HIF-1α, a key gene of hypoxic environment, as tools for post-mortem time estimation.

Salomé Mascarell, Coralie Torrens, Caroline Andrique, Asmaa Foda, Tania Delabarde, Bertrand Ludes, Anne-Margaux Collignon, Anne Poliard

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

8 authors.

Salomé MascarellImaging and Biothérapies Laboratory URP2496, Université Paris Cité, Orofacial Pathologies, Dental School, Montrouge, 92120, France.ORCID 0000-0003-3509-8880
Coralie TorrensImaging and Biothérapies Laboratory URP2496, Université Paris Cité, Orofacial Pathologies, Dental School, Montrouge, 92120, France.
Caroline AndriqueImaging and Biothérapies Laboratory URP2496, Université Paris Cité, Orofacial Pathologies, Dental School, Montrouge, 92120, France.ORCID 0000-0002-0447-9616
Asmaa FodaImaging and Biothérapies Laboratory URP2496, Université Paris Cité, Orofacial Pathologies, Dental School, Montrouge, 92120, France.
Tania DelabardeInstitut Médico-Légal, Paris, 75012, France.
Bertrand LudesInstitut Médico-Légal, Paris, 75012, France.
Anne-Margaux CollignonImaging and Biothérapies Laboratory URP2496, Université Paris Cité, Orofacial Pathologies, Dental School, Montrouge, 92120, France.
Anne PoliardImaging and Biothérapies Laboratory URP2496, Université Paris Cité, Orofacial Pathologies, Dental School, Montrouge, 92120, France.ORCID 0000-0003-2285-1909

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The post-mortem interval (PMI) is the time elapsed between the death of an individual and its forensic examination. It is a crucial information for judicial authorities, but current techniques still cannot establish a precise time interval. Novel approaches are therefore required. Recently, gingival tissue has emerged as interesting for forensic analysis thanks to the protection offered by lips to this tissue, limiting the influence of environmental factors. It is also easily accessible, and its sampling is minimally invasive even in the presence of rigor mortis. Moreover, the expression of HIF-1α, a master mediator of the hypoxic environment, has been described in gingival samples at different post-mortem (PM) times. We have hypothesized that the time-dependent post-mortem expression of HIF-1α could serve as a biomarker to more accurately predict the PMI. Our analyses were performed in an animal model, the mouse, where environment can be precisely controlled. Therewith, gingival tissue morphology was evaluated through histochemical staining and HIF-1α expression was analyzed by qPCR, western blots and immunofluorescence at different post-mortem times (0h to 100h). Our results showed (a) a global post-mortem stability of gingival tissue (b) a rapid increase in HIF-1α mRNA expression in the short post-mortem times followed by a slow decrease in transcript expression until 100h PM (c) an expression of the HIF- 1α protein and its degradation products, that follows the mRNA pattern (d) the presence of HIF-1α protein in the epithelial and connective layers of the tissue, with signal accumulation in both gingival strata until at least 32h post-mortem. This pilot study thus validated the mouse and the gingival tissue as models for post-mortem analyses, as well as for studying the fate of proteins such as HIF-1α. Transferring these approaches to human subjects may provide a more accurate estimate of PMI.

Indexed as

GingivaHypoxia-Inducible Factor 1, alpha SubunitPostmortem ChangesAnimalsHypoxiaMaleMiceMice, Inbred C57BLTime FactorsHif1a protein, mouseHypoxia-Inducible Factor 1, alpha Subunit

Identifiers

PMID39546465
PMCPMC11567532

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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.