Literature DB >> 29312506

A comparison of apoptosis levels in keloid tissue, physiological scars and normal skin.

Ming-Zi Zhang1, Xin-Hang Dong1, En-Ling Guan2, Lou-Bin Si1, Rui-Qi Zhuge3, Peng-Xiang Zhao4, Xin Zhang4, Meng-Yu Liu4, Yao Mawulikplimi Adzavon4, Xiao Long1, Zheng Qi1, Xiaojun Wang1.   

Abstract

Apoptosis is a process of programmed cell death that occurs in multicellular organisms. The mitochondrial pathway plays a paramount role in apoptosis. In this study, the expression levels of key factors in the mitochondrial pathway and the cell proliferation factor (PCNA) were measured to evaluate the level of apoptosis and proliferation in keloid scars, physiological scars and normal skin tissue. Thirty samples were taken from 30 patients: 10 keloid patients, 10 physiological scar patients and 10 patients without obvious scarring. All 30 patients were selected randomly from the Department of Plastic Surgery at Peking Union Medical College Hospital from June 2016 to December 2016. Hematoxylin and eosin staining and Masson staining were used to observe the differences in histology and fiber tissue content. Mitochondrial pathway factors (caspase-3, caspase-8, caspase-9, Bcl-2, Bax, cytochrome-c) and PCNA expression levels were detected by immunohistochemistry and were analyzed as the percentage of positively stained cells in the epidermis and dermis. Relative protein expression levels were measured by western blotting. Compared with physiological scars and normal skin tissue, keloid tissue had an increase in fiber number and decrease in cell content. In our immunohistochemical and western blot analyses, all tissue types showed similar expression levels of the mitochondrial pathway factors. However, the percentage of PCNA-positive cells and the relative protein expression level of PCNA were significantly higher in keloid tissue. Keloid has a similar apoptosis level as physiological scars and normal skin but has a higher expression of PCNA, indicating that keloid scars have high levels of proliferation and normal apoptosis.

Entities:  

Keywords:  Keloid; apoptosis; physiological scar; proliferation; skin

Year:  2017        PMID: 29312506      PMCID: PMC5752904     

Source DB:  PubMed          Journal:  Am J Transl Res            Impact factor:   4.060


  31 in total

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Journal:  Plast Reconstr Surg       Date:  2001-10       Impact factor: 4.730

Review 2.  Keloids--clinical diagnosis, pathogenesis, and treatment options.

Authors:  Alexander G Marneros; Thomas Krieg
Journal:  J Dtsch Dermatol Ges       Date:  2004-11       Impact factor: 5.584

Review 3.  PCNA, the maestro of the replication fork.

Authors:  George-Lucian Moldovan; Boris Pfander; Stefan Jentsch
Journal:  Cell       Date:  2007-05-18       Impact factor: 41.582

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Authors:  Daniel J Rosen; Mitesh K Patel; Katherine Freeman; Paul R Weiss
Journal:  Plast Reconstr Surg       Date:  2007-10       Impact factor: 4.730

5.  Lipid nano-bubble combined with ultrasound for anti-keloids therapy.

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6.  The surgical treatment of keloids.

Authors:  S V Pollack; J B Goslen
Journal:  J Dermatol Surg Oncol       Date:  1982-12

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Journal:  J Oral Maxillofac Surg       Date:  2007-07       Impact factor: 1.895

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Authors:  Rafael M C Melo; Yuri S Martins; Ronald K Luz; Elizete Rizzo; Nilo Bazzoli
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10.  Chemokine-Like Factor 1 (CKLF-1) is Overexpressed in Keloid Patients: A Potential Indicating Factor for Keloid-Predisposed Individuals.

Authors:  Mingzi Zhang; Ying Xu; Yifang Liu; Yingying Cheng; Pengxiang Zhao; Hao Liu; Youbin Wang; Xuemei Ma
Journal:  Medicine (Baltimore)       Date:  2016-03       Impact factor: 1.889

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  10 in total

1.  A Signature of Genes Featuring FGF11 Revealed Aberrant Fibroblast Activation and Immune Infiltration Properties in Keloid Tissue.

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2.  Downregulation of PLK4 expression induces apoptosis and G0/G1-phase cell cycle arrest in keloid fibroblasts.

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3.  Integrated Interaction Network of MicroRNA Target Genes in Keloid Scarring.

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Journal:  Mol Diagn Ther       Date:  2019-02       Impact factor: 4.074

4.  [Focused ultrasound therapy for reducing recurrence of vulvar lichen simplex chronicus in rats: efficacy and mechanism].

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5.  Dermal fibroblast phagocytosis of apoptotic cells: A novel pathway for wound resolution.

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6.  Extracellular Vesicles from a Three-Dimensional Culture of Perivascular Cells Accelerate Skin Wound Healing in a Rat.

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7.  Striae Distensae: In Vitro Study and Assessment of Combined Treatment with Sodium Ascorbate and Platelet-Rich Plasma on Fibroblasts.

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Journal:  Aesthetic Plast Surg       Date:  2021-06-01       Impact factor: 2.326

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Journal:  Aesthetic Plast Surg       Date:  2021-05-10       Impact factor: 2.708

9.  Effect of Co-transplanting Stromal Vascular Fraction-Gelatin and Platelet-Rich Fibrin on the Long-Term Maintenance of Fat Volume.

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Journal:  Aesthetic Plast Surg       Date:  2021-04-14       Impact factor: 2.708

10.  Keloid pathophysiology: fibroblast or inflammatory disorders?

Authors:  Ferdinand W Nangole; George W Agak
Journal:  JPRAS Open       Date:  2019-11-05
  10 in total

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