Evidence map›Paper›PMID 35682813›Full record

ReviewInternational journal of molecular sciences2022

Age-Related Changes in the Fibroblastic Differon of the Dermis: Role in Skin Aging.

Alla Zorina, Vadim Zorin, Dmitry Kudlay, Pavel Kopnin

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. AClinical, cosmetic and investigational dermatology · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Epigallocatechin Gallate inPharmaceuticals (Basel, Switzerland) · 2025
    Article
  9. Article
  10. Article
  11. UnripePreventive nutrition and food science · 2023
    Article
  12. Review
  13. Article
  14. Utilizing deep learning for dermal matrix quality assessment on in vivo line-field confocal optical coherence tomography images.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2023
    Article
  15. Article
  16. Article
  17. Cellular Senescence in Physiological and Pathological Processes.International journal of molecular sciences · 2022
    Article
  18. Review
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

4 authors at 3 institutions in 1 country.

Alla ZorinaHuman Stem Cells Institute, 119333 Moscow, Russia.
Vadim ZorinHuman Stem Cells Institute, 119333 Moscow, Russia.
Dmitry KudlayDepartment of Pharmacology, Institute of Pharmacy, I. M. Sechenov First Moscow State Medical University (Sechenov University), 119991 Moscow, Russia.ORCID 0000-0003-1878-4467
Pavel KopninN. N. Blokhin National Medical Research Oncology Center, Ministry of Health of Russia, 115478 Moscow, Russia.ORCID 0000-0002-2078-4274
Human Stem Cells Institute PJSC (Russia) · RUMinistry of Health of the Russian Federation · RUSechenov University · RU

Funding

Russian Science Foundation № 20-15-00321
6 · The paper itself

Abstract

Skin aging is a multi-factorial process that affects nearly every aspect of skin biology and function. The processes developing in the skin during aging are based on fundamental molecular mechanisms associated with fibroblasts, the main cellular population of the dermis. It has been revealed that the amount of fibroblasts decreases markedly with age and their functional activity is also reduced. This inevitably leads to a decrease in the regenerative abilities of the skin and the progression of its aging. In this review we consider the mechanisms underlying these processes, mainly the changes observed with age in the stem/progenitor cells that constitute the fibroblastic differon of the dermis and form their microenvironment (niches). These changes lead to the depletion of stem cells, which, in turn, leads to a decrease in the number of differentiated (mature) dermal fibroblasts responsible for the production of the dermal extracellular matrix and its remodeling. We also describe in detail DNA damages, their cellular and systemic consequences, molecular mechanisms of DNA damage response, and also the role of fibroblast senescence in skin aging.

Indexed as

Skin AgingDermisExtracellular MatrixFibroblastsSkinagingfibroblastsskinstem cells

Identifiers

PMID35682813
PMCPMC9181700
OpenAlexW4281691456

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.