Evidence map›Paper›PMID 32903493›Full record

ArticleFrontiers in bioengineering and biotechnology2020

Bases for Treating Skin Aging With Artificial Mitochondrial Transfer/Transplant (AMT/T).

Micaela Balcázar, Stalin Cañizares, Tatiana Borja, Patricia Pontón, Sirivanh Bisiou, Eva Carabasse, Angela Bacilieri, Celia Canavese, Ramiro F Diaz, Francisco Cabrera and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  4. International journal of molecular sciences · 2025
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  6. Article
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  9. Mitochondria makeover: unlocking the path to healthy longevity.Expert opinion on therapeutic targets · 2024
    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

11 authors at 3 institutions in 2 countries.

Micaela BalcázarEscuela de Medicina, Colegio de Ciencias de la Salud COCSA, Universidad San Francisco de Quito USFQ, Quito, Ecuador.
Stalin CañizaresEscuela de Medicina, Colegio de Ciencias de la Salud COCSA, Universidad San Francisco de Quito USFQ, Quito, Ecuador.
Tatiana BorjaServicio de Patología, Hospital Voz Andes, Quito, Ecuador.
Patricia PontónServicio de Patología, Hospital Voz Andes, Quito, Ecuador.
Sirivanh BisiouUniversité de Montpellier, Faculté de Medicine, Montpellier, France.
Eva CarabasseUniversité de Montpellier, Faculté de Medicine, Montpellier, France.
Angela BacilieriUniversité de Montpellier, Faculté de Medicine, Montpellier, France.
Celia CanaveseUniversité de Montpellier, Faculté de Medicine, Montpellier, France.
Ramiro F DiazEscuela de Medicina Veterinaria, Colegio de Ciencias de la Salud COCSA, Universidad San Francisco de Quito USFQ, Quito, Ecuador.
Francisco CabreraEscuela de Medicina Veterinaria, Colegio de Ciencias de la Salud COCSA, Universidad San Francisco de Quito USFQ, Quito, Ecuador.
Andrés CaicedoEscuela de Medicina, Colegio de Ciencias de la Salud COCSA, Universidad San Francisco de Quito USFQ, Quito, Ecuador.
Universidad San Francisco de Quito · ECUniversité de Montpellier · FRHospital Vozandes · EC

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The perception of mitochondria as only the powerhouse of the cell has dramatically changed in the last decade. It is now accepted that in addition to being essential intracellularly, mitochondria can promote cellular repair when transferred from healthy to damaged cells. The artificial mitochondria transfer/transplant (AMT/T) group of techniques emulate this naturally occurring process and have been used to develop therapies to treat a range of diseases including cardiac and neurodegenerative. Mitochondria accumulate damage with time, resulting in cellular senescence. Skin cells and its mitochondria are profoundly affected by ultraviolet radiation and other factors that induce premature and accelerated aging. In this article, we propose the basis to use AMT/T to treat skin aging by transferring healthy mitochondria to senescent cells, possibly revitalizing them. We provide insightful information about how skin structure, components, and cells could age rapidly depending on the amount of damage received. Arguments are shown in favor of the use of AMT/T to treat aging skin and its cells, among them the possibility to stop free radical production, add new genetic material, and provide an energetic boost to help cells prolong their viability over time. This article intends to present one of the many aspects in which mitochondria could be used as a universal treatment for cell and tissue damage and aging.

Indexed as

agingartificial mitochondria transfer transplant (AMT/T)MitoCeptionmitochondriaregenerative medicinesenescenceskin

Identifiers

PMID32903493
PMCPMC7438394
OpenAlexW3049358235

What OpenQuestion 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 OpenQuestion graph.