Evidence map›Paper›PMID 37209167›Full record

ArticleArchives of dermatological research2023

Differential expression of extracellular matrix proteins in the lesional skin of vitiligo patients.

Seema Rani, Naveed Pervaiz, Davinder Parsad, Ravinder Kumar

Abstract read
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In one paragraph

Article in Archives of dermatological research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. An Overview of the Biological Complexity of Vitiligo.Oxidative medicine and cellular longevity · 2024
    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 4 institutions in 2 countries.

Seema RaniDepartment of Zoology, Hindu Girls College, Sonepat, 131001, India.
Naveed PervaizDepartment of Pharmaceutical Sciences, The University of Tennessee Health Science Center, Memphis, TN, USA.
Davinder ParsadDepartment of Dermatology Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Ravinder KumarDepartment of Zoology, Hindu Girls College, Sonepat, 131001, India. ravinder@pu.ac.in.
Hindu College of Pharmacy · INPanjab University · INPost Graduate Institute of Medical Education and Research · INUniversity of Tennessee Health Science Center · US

Funding

DST-INSPIRE Faculty Project, New Delhi [IFA11-LSBM-61] to Ravinder Kumar, and DST-INSPIRE fellowship [IF140212] to Seema Rani. IFA11-LSBM-61/ IF140212
6 · The paper itself

Abstract

Skin pigmentation is regulated by intricate interaction of the dermis and epidermis. The extracellular components present in the dermis play a very important role in the maintenance of skin homeostasis. Therefore, our objective was to check the expression of various ECM components secreted by the dermal fibroblasts in the lesional skin and non-lesional skin of vitiligo patients. For this study, skin punch biopsies (4 mm) were collected from lesional skin (n = 12), non-lesional skin (n = 6) of non-segmental vitiligo patient's (NSV) and healthy control skin (n = 10). Masson's trichrome staining was performed to check the collagen fibre. The expression of collagen type 1, IV, elastin, fibronectin, E-cadherin and integrin β1 was checked by real-time PCR and immunohistochemistry. In this study, we demonstrated an increased expression of collagen type 1 in the lesional skin of vitiligo patients. The expression of collagen type IV, fibronectin, elastin and adhesion components such as E-cadherin and integrin β1 was observed to be significantly decreased in the lesional skin of NSV patients as compared to healthy control, whereas insignificant difference was observed between non-lesional and control skin. Increased expression of collagen type 1 in the lesional skin of vitiligo patients might be inhibiting the migration of melanocytes, whereas the decreased expression of elastin, collagen type IV, fibronectin, E-cadherins and integrins in the lesional skin may inhibit adhesion, migration, growth and differentiation of cells.

Indexed as

VitiligoCadherinsCollagen Type IVElastinExtracellular MatrixExtracellular Matrix ProteinsFibronectinsHumansIntegrin beta1MelanocytesSkinCadherinsCollagen Type IVElastinExtracellular Matrix ProteinsFibronectinsIntegrin beta1Adhesion moleculesExtracellular matrix componentsVitiligo

Identifiers

PMID37209167
OpenAlexW4377138567

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.