Long noncoding RNA XIST promotes cell proliferation and migration in diabetic foot ulcers through the miR-126-3p/EGFR axis
Open Access
- 6 February 2024
- journal article
- research article
- Published by Springer Nature in Diabetology & Metabolic Syndrome
- Vol. 16 (1) , 1-14
Abstract
Background: The prevalence of diabetic foot ulcers (DFUs) has caused serious harm to human health. To date, a highly effective treatment is lacking. Long noncoding RNA X-inactive specific transcript (lncRNA XIST) has been the subject of mounting research studies, all of which have found that it serves as a protective factor against certain diseases; however, its function in DFUs is not entirely understood. This study was performed to determine the importance of the lncRNA XIST in the pathogenesis and biological function of DFUs. Methods: Diabetic ulcer skin from rats was analysed using haematoxylin-eosin (HE), Masson’s trichrome, and immunohistochemistry (IHC) staining. The differences in the expression of genes and proteins were examined with real-time quantitative polymerase chain reaction (RT–qPCR) and Western blotting. Next, the interaction was verified with a dual luciferase gene reporter assay. In addition, CCK-8, Transwell, and wound healing assays were used to assess the proliferation and migration of HaCaT cells. Results: The lncRNA XIST and epidermal growth factor receptor (EGFR) were downregulated, while microRNA-126-3p (miR-126-3p) was increased in diabetic ulcer rat skin tissues and high glucose-induced HaCaT cells. In addition, we found that the lncRNA XIST binds to miR-126-3p and that EGFR is directly targeted by miR‑126‑3p. Silencing XIST contributed to upregulated miR-126-3p expression, thus lowering EGFR levels and inhibiting the proliferative and migratory abilities of high glucose-treated HaCaT cells; however, the miR-126-3p inhibitor and overexpression of EGFR reversed this effect. Conclusion: Decreased lncRNA XIST expression inhibits the proliferative and migratory abilities of high glucose-induced HaCaT cells by modulating the miR-126-3p/EGFR axis, causing delayed wound healing.Keywords
Funding Information
- National Natural Science Foundation of China (81960352)
- National Natural Science Foundation of China (82160376, 82160380)
- Jiangxi Provincial Department of Science and Technology GanPo 555 Project leading personnel training Program (1210013001)
- Provincial Natural Science Foundation of China (20232BAB206082)
This publication has 41 references indexed in Scilit:
- Global aetiology and epidemiology of type 2 diabetes mellitus and its complicationsNature Reviews Endocrinology, 2017
- Diabetic wound regeneration using peptide-modified hydrogels to target re-epithelializationProceedings of the National Academy of Sciences, 2016
- Endogenous microRNA sponges: evidence and controversyNature Reviews Genetics, 2016
- WHS guidelines update: Diabetic foot ulcer treatment guidelinesWound Repair and Regeneration, 2016
- Interdependent epidermal growth factor receptor signalling and traffickingThe International Journal of Biochemistry & Cell Biology, 2014
- Diabetic foot ulcersJournal of the American Academy of Dermatology, 2014
- Epidermal Growth Factor and Epidermal Growth Factor Receptor: The Yin and Yang in the Treatment of Cutaneous Wounds and CancerAdvances in Wound Care, 2013
- Association between TNFRSF11B gene polymorphisms and history of ischemic stroke in Italian diabetic patientsHuman Genetics, 2012
- High Glucose Suppresses Epidermal Growth Factor Receptor/Phosphatidylinositol 3-Kinase/Akt Signaling Pathway and Attenuates Corneal Epithelial Wound HealingDiabetes, 2009
- Contributions of the epidermal growth factor receptor to keratinocyte motilityMicroscopy Research and Technique, 1998