Evidence map›Paper›PMID 28880199›Full record

ArticleInternational journal of molecular sciences2017

The Role of Focal Adhesion Kinase in Keratinocyte Fibrogenic Gene Expression.

Michael Januszyk, Sun Hyung Kwon, Victor W Wong, Jagannath Padmanabhan, Zeshaan N Maan, Alexander J Whittam, Melanie R Major, Geoffrey C Gurtner

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Fibroblasts in Scar Formation: Biology and Clinical Translation.Oxidative medicine and cellular longevity · 2022
    Pooled it
  3. A Marine-Derived Steroid fromMarine drugs · 2025
    Article
  4. Article
  5. Review
  6. Advances in pharmacological and pharmaceutical sciences · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. FAK in Cancer: From Mechanisms to Therapeutic Strategies.International journal of molecular sciences · 2022
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Mechanotransduction in Wound Healing and Fibrosis.Journal of clinical medicine · 2020
    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

8 authors at 1 institution in 1 country.

Michael JanuszykHagey Laboratory, Division of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305-5148, USA. mjanuszyk@mednet.ucla.edu.
Sun Hyung KwonHagey Laboratory, Division of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305-5148, USA. kwonsunh@stanford.edu.
Victor W WongHagey Laboratory, Division of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305-5148, USA. vicw.wong@gmail.com.
Jagannath PadmanabhanHagey Laboratory, Division of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305-5148, USA. jaganpa@stanford.edu.
Zeshaan N MaanHagey Laboratory, Division of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305-5148, USA. zmaan@stanford.edu.
Alexander J WhittamHagey Laboratory, Division of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305-5148, USA. alexander.whittam@gmail.com.
Melanie R MajorHagey Laboratory, Division of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305-5148, USA. melaniermajor@gmail.com.
Geoffrey C GurtnerHagey Laboratory, Division of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305-5148, USA. ggurtner@stanford.edu.
Stanford University · US

Funding

POSTDOCTORAL TRAINING IN MEDICAL INFORMATION SCIENCEST15LM007033 · NLM · STANFORD UNIVERSITY · PI SYLVIA KATINA PLEVRITIS · 1985 to 2026
$25.5M
NLM NIH HHS T15 LM007033
6 · The paper itself

Abstract

Abnormal skin scarring causes functional impairment, psychological stress, and high socioeconomic cost. Evidence shows that altered mechanotransduction pathways have been linked to both inflammation and fibrosis, and that focal adhesion kinase (FAK) is a key mediator of these processes. We investigated the importance of keratinocyte FAK at the single cell level in key fibrogenic pathways critical for scar formation. Keratinocytes were isolated from wildtype and keratinocyte-specific FAK-deleted mice, cultured, and sorted into single cells. Keratinocytes were evaluated using a microfluidic-based platform for high-resolution transcriptional analysis. Partitive clustering, gene enrichment analysis, and network modeling were applied to characterize the significance of FAK on regulating keratinocyte subpopulations and fibrogenic pathways important for scar formation. Considerable transcriptional heterogeneity was observed within the keratinocyte populations. FAK-deleted keratinocytes demonstrated increased expression of genes integral to mechanotransduction and extracellular matrix production, including Igtbl, Mmpla, and Col4a1. Transcriptional activities upon FAK deletion were not identical across all single keratinocytes, resulting in higher frequency of a minor subpopulation characterized by a matrix-remodeling profile compared to wildtype keratinocyte population. The importance of keratinocyte FAK signaling gene expression was revealed. A minor subpopulation of keratinocytes characterized by a matrix-modulating profile may be a keratinocyte subset important for mechanotransduction and scar formation.

Indexed as

AnimalsExtracellular MatrixFocal Adhesion Protein-Tyrosine KinasesFocal AdhesionsHumansKeratinocytesMechanotransduction, CellularMice, KnockoutSignal TransductionFocal Adhesion Protein-Tyrosine Kinasesextracellular matrixfocal adhesion kinasehypertrophic scarkeratinocytemechanotransductionsingle-cell transcriptional analysisskin fibrosistranscriptomics

Identifiers

PMID28880199
PMCPMC5618564
OpenAlexW2750600358

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.