Evidence map›Paper›PMID 35269458›Full record

ArticleCells2022

MiR-30a-5p Alters Epidermal Terminal Differentiation during Aging by Regulating BNIP3L/NIX-Dependent Mitophagy.

Fabien P Chevalier, Julie Rorteau, Sandra Ferraro, Lisa S Martin, Alejandro Gonzalez-Torres, Aurore Berthier, Naima El Kholti, Jérôme Lamartine

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% of its field
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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Article
  5. Review
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  7. Review
  8. Role of Mitochondrial Dynamics in Skin Homeostasis: An Update.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Review
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  12. Article
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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 at 1 institution in 1 country.

Fabien P ChevalierCNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007 Lyon, France.ORCID 0000-0001-8034-8661
Julie RorteauCNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007 Lyon, France.
Sandra FerraroCNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007 Lyon, France.
Lisa S MartinCNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007 Lyon, France.
Alejandro Gonzalez-TorresCNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007 Lyon, France.
Aurore BerthierCNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007 Lyon, France.
Naima El KholtiCNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007 Lyon, France.
Jérôme LamartineCNRS UMR 5305, Tissue Biology and Therapeutic Engineering Laboratory (LBTI), 69007 Lyon, France.
Université Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronological aging is characterized by an alteration in the genes' regulatory network. In human skin, epidermal keratinocytes fail to differentiate properly with aging, leading to the weakening of the epidermal function. MiR-30a is particularly overexpressed with epidermal aging, but the downstream molecular mechanisms are still uncovered. The aim of this study was to decipher the effects of miR-30a overexpression in the human epidermis, with a focus on keratinocyte differentiation. We formally identified the mitophagy receptor BNIP3L as a direct target of miR-30a. Using a 3D organotypic model of reconstructed human epidermis overexpressing miR-30a, we observed a strong reduction in BNIP3L expression in the granular layer. In human epidermal sections of skin biopsies from donors of different ages, we observed a similar pattern of BNIP3L decreasing with aging. Moreover, human primary keratinocytes undergoing differentiation in vitro also showed a decreased expression of

Indexed as

MicroRNAsMitophagyAgingApoptosis Regulatory ProteinsEpidermisHumansMembrane ProteinsProto-Oncogene ProteinsTumor Suppressor ProteinsApoptosis Regulatory ProteinsBNIP3L protein, humanMembrane ProteinsMicroRNAsProto-Oncogene ProteinsTumor Suppressor ProteinsagingBNIP3LkeratinocytemiR-30amitochondriamitophagy

Identifiers

PMID35269458
PMCPMC8909909
OpenAlexW4214541473

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.