Evidence map›Paper›PMID 33543036›Full record

ArticleMatrix biology plus2020

Alterations in extracellular matrix composition during aging and photoaging of the skin.

Maxwell C McCabe, Ryan C Hill, Kenneth Calderone, Yilei Cui, Yan Yan, Taihao Quan, Gary J Fisher, Kirk C Hansen

Open access · goldAbstract read
In one paragraph

Article in Matrix biology plus, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
15.3field-weighted citation impact, top 1% 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

84 citing papers in PubMed, 164 citations in OpenAlex.

  1. Article
  2. LiposomalInternational journal of molecular sciences · 2026
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24 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Maxwell C McCabeDepartment of Biochemistry and Molecular Genetics, School of Medicine, University of Colorado, 12801 E 17th Ave., Aurora, CO 80045, USA.
Ryan C HillDepartment of Biochemistry and Molecular Genetics, School of Medicine, University of Colorado, 12801 E 17th Ave., Aurora, CO 80045, USA.
Kenneth CalderoneDepartment of Dermatology, University of Michigan, 1150 W. Medical Center Drive, Medical Science I R6447, Ann Arbor, MI 48109, USA.
Yilei CuiDepartment of Dermatology, University of Michigan, 1150 W. Medical Center Drive, Medical Science I R6447, Ann Arbor, MI 48109, USA.
Yan YanDepartment of Dermatology, University of Michigan, 1150 W. Medical Center Drive, Medical Science I R6447, Ann Arbor, MI 48109, USA.
Taihao QuanDepartment of Dermatology, University of Michigan, 1150 W. Medical Center Drive, Medical Science I R6447, Ann Arbor, MI 48109, USA.
Gary J FisherDepartment of Dermatology, University of Michigan, 1150 W. Medical Center Drive, Medical Science I R6447, Ann Arbor, MI 48109, USA.
Kirk C HansenDepartment of Biochemistry and Molecular Genetics, School of Medicine, University of Colorado, 12801 E 17th Ave., Aurora, CO 80045, USA.
University of Michigan–Ann Arbor · USUniversity of Colorado Denver · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human skin is composed of the cell-rich epidermis, the extracellular matrix (ECM) rich dermis, and the hypodermis. Within the dermis, a dense network of ECM proteins provides structural support to the skin and regulates a wide variety of signaling pathways which govern cell proliferation and other critical processes. Both intrinsic aging, which occurs steadily over time, and extrinsic aging (photoaging), which occurs as a result of external insults such as solar radiation, cause alterations to the dermal ECM. In this study, we utilized both quantitative and global proteomics, alongside single harmonic generation (SHG) and two-photon autofluorescence (TPAF) imaging, to assess changes in dermal composition during intrinsic and extrinsic aging. We find that both intrinsic and extrinsic aging result in significant decreases in ECM-supporting proteoglycans and structural ECM integrity, evidenced by decreasing collagen abundance and increasing fibril fragmentation. Intrinsic aging also produces changes distinct from those produced by photoaging, including reductions in elastic fiber and crosslinking enzyme abundance. In contrast, photoaging is primarily defined by increases in elastic fiber-associated protein and pro-inflammatory proteases. Changes associated with photoaging are evident even in young (mid 20s) sun-exposed forearm skin, indicating that proteomic evidence of photoaging is present decades prior to clinical signs of photoaging. GO term enrichment revealed that both intrinsic aging and photoaging share common features of chronic inflammation. The proteomic data has been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the data set identifier PXD015982.

Indexed as

AgingAUC, area under the curveCE, cornified envelopeCNBr, cyanogen bromideCollagenECM, extracellular matrixExtracellular matrixGO, gene ontologyiECM, insoluble ECMPhotoagingProteomicsQconCATs, quantitative concatemerssECM, soluble ECMSHG, single harmonic generationSkinTPAF, two-photon autofluorescenceUV, ultraviolet

Identifiers

PMID33543036
PMCPMC7852213
OpenAlexW3036810437

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.