Evidence map›Paper›PMID 36293511›Full record

ArticleInternational journal of molecular sciences2022

Collagen V α1 Chain Decrease in Papillary Dermis from Early Systemic Sclerosis: A New Proposal in Cutaneous Fibrosis Molecular Structure.

Jymenez de Morais, Ana Paula P Velosa, Priscila C Andrade, Denise Frediani, Solange Carrasco, Zelita A de Jesus Queiroz, Patrícia Martin, Renata F Saito, Vitória Elias, Cláudia Goldenstein-Schainberg and 4 more

Open access · goldAbstract read
In one paragraph

Article 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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

14 authors at 2 institutions in 1 country.

Jymenez de MoraisDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Ana Paula P VelosaDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Priscila C AndradeDepartment of Pathology, Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Denise FredianiDiscipline of Clinical Emergency (LIM 51), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Solange CarrascoDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0003-2469-9744
Zelita A de Jesus QueirozDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Patrícia MartinDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Renata F SaitoCenter for Translational Research in Oncology (LIM24), Department of Radiology and Oncology, Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Vitória EliasDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Cláudia Goldenstein-SchainbergDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0003-3306-9699
Roger ChammasCenter for Translational Research in Oncology (LIM24), Department of Radiology and Oncology, Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0003-0342-8726
Percival D Sampaio-BarrosDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Vera L CapelozziDepartment of Pathology, Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0001-9732-5853
Walcy R TeodoroDivision of Rheumatology (LIM 17), Faculdade de Medicina da Universidade de São Paulo, São Paulo 01246-903, Brazil.
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRInstituto do Câncer do Estado de São Paulo · BR

Funding

São Paulo Research Foundation 2018/00415-0; 2018/20403-6; 2021/13220-5
6 · The paper itself

Abstract

Cutaneous fibrosis is one of the main features of systemic sclerosis (SSc). Recent findings correlated abnormal collagen V (Col V) deposition in dermis with skin thickening and disease activity in SSc. Considering that Col V is an important regulator of collagen fibrillogenesis, understanding the role of Col V in the first two years of the skin fibrosis in SSc (early SSc) can help to determine new targets for future treatments. In this study, we analyzed the morphological, ultrastructural and molecular features of α1(V) and α2(V) chains and the expression of their coding genes COL5A1 and COL5A2 in collagen fibrillogenesis in early-SSc. Skin biopsies were obtained from seven consecutive treatment-naïve patients with SSc-related fibrosis and four healthy controls. Our data showed increased α1(V) and α2(V) chain expression in the reticular dermis of early-SSc patients; however, immunofluorescence and ultrastructural immunogold staining determined a significant decreased expression of the α1(V) chain along the dermoepidermal junction in the papillary dermis from early-SSc-patients in relation to the control (12.77 ± 1.34 vs. 66.84 ± 3.36; p < 0.0001). The immunoblot confirmed the decreased expression of the α1(V) chain by the cutaneous fibroblasts of early-SSc, despite the increased COL5A1 and COL5A2 gene expression. In contrast, the α2(V) chain was overexpressed in the small vessels (63.18 ± 3.56 vs. 12.16 ± 0.81; p < 0.0001) and capillaries (60.88 ± 5.82 vs. 15.11 ± 3.80; p < 0.0001) in the reticular dermis of early-SSc patients. Furthermore, COLVA2 siRNA in SSc cutaneous fibroblasts resulted in a decreased α1(V) chain expression. These results highlight an intense decrease in the α1(V) chain along the dermoepidermal junction, suggesting an altered molecular histoarchitecture in the SSc papillary dermis, with a possible decrease in the expression of the α1(V)3 homotrimeric isoform, which could interfere with the thickening and cutaneous fibrosis related to SSc.

Indexed as

DermisScleroderma, SystemicCollagenFibroblastsFibrosisHumansMolecular StructureRNA, Small InterferingSkinCollagenRNA, Small Interferingcollagen V alpha chainsfibrosispapillary dermisskinsystemic sclerosis

Identifiers

PMID36293511
PMCPMC9604101
OpenAlexW4307266407

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.