Your new experience awaits. Try the new design now and help us make it even better

EDITORIAL article

Front. Endocrinol., 11 July 2025

Sec. Diabetes: Molecular Mechanisms

Volume 16 - 2025 | https://doi.org/10.3389/fendo.2025.1650648

This article is part of the Research TopicDiabetic Wound: Multifaceted Mechanisms and Future of Diabetic Wound Healing, Volume IIView all 7 articles

Editorial: Diabetic wound: multifaceted mechanisms and future of diabetic wound healing, volume II

  • 1Division of Endocrinology, Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
  • 2Hubei Clinical Medical Research Center for Endocrinology and Metabolic Diseases, Hubei, China
  • 3Branch of National Clinical Research Center for Metabolic Diseases, Hubei, China
  • 4Department of Podiatry, National University Hospital Singapore, Singapore, Singapore
  • 5Department of Endocrinology and Metabolism, West China Hospital of Sichuan University, Chengdu, China

Diabetic foot ulcer (DFU) represents a severe complication of diabetes, which will develop in an estimated 15%-25% of diabetic patients globally during their lifetime (1). DFU is associated with significant disability and mortality rates, with reported annual mortality rate of 11% and mortality rate among those who undergo amputation surgery exceeding 22% (2). The management of DFU continues to pose substantial clinical challenges. Six recent studies published in “Diabetic wound: multifaceted mechanisms and future of diabetic wound healing, volume II” shed light on innovative therapeutic strategies that may help to transform patient outcomes.

Mesenchymal stem cells (MSCs) have been recently widely investigated in the field of wound management due to their powerful regenerative capabilities and immunomodulatory properties (3, 4). Of note, the regenerative effects of MSCs are mainly attributed to extracellular vesicles (EVs). A meta-analysis by Yue et al. on MSC-derived small EVs (MSC-sEVs) included 21 preclinical studies, which reported that MSC-sEVs could significantly enhance wound closure, angiogenesis, collagen deposition, and anti-inflammatory responses in type 2 diabetic models. Notably, local injection may be the optimal route of administration for EVs due to their rapid systemic clearance. Despite these promising results, the clinical translation of sEVs faces several hurdles, such as standardization of isolation methods, scalability, and safety concerns. Rigorous randomized controlled trials (RCTs) to validate these findings in humans are needed.

Complementing this, Aghayants et al. provide a comprehensive review of non-coding RNAs (ncRNAs) as regulators of diabetic wound healing. Their work elucidates the roles of microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs) in modulating inflammation, angiogenesis, and tissue remodeling. The study indicated that the recent advancement in nanomedicine may contribute to the therapeutic promise of ncRNA-based interventions by improving the stability and targeting precision of exogenous ncRNAs.

Fibrous proteins, particularly collagen and elastin, serve as key structural components of the extracellular matrix (ECM), which play a critical role in wound repair and tissue regeneration (5). Yan et al.’s review on fibrous proteins underscores the potential of biomaterials to revolutionize diabetic wound care. The authors emphasize that advanced wound dressings incorporating fibrous proteins offer bioactive properties that go beyond traditional passive dressings. These materials not only provide structural support but also modulate cellular behavior, promote angiogenesis, and reduce oxidative stress. However, most of the literature cited in this review are animal experimental articles and clinical evidences are limited.

Ni et al. offered a therapeutic potential of a traditional Chinese medicine (TCM) formulation, Danggui Sini decoction (DSD). DSD is a TCM prescription with a long history of use for blood deficiency and cold coagulation syndromes. Using network pharmacology and molecular docking, the authors identify that the major molecular pathways of DSD may be mediated by AGE-RAGE and PI3K-AKT signaling. Their meta-analysis of six RCTs with a total of 444 patients further validates DSD’s efficacy on the improvement of wound repair and ankle-brachial index.

Interestingly, Guan et al. investigate machine learning (ML)’s applications in DFU, emphasizing its capacity to analyze complex datasets from imaging, biomarkers, and clinical biomechanics. ML algorithms, such as convolutional neural networks (CNNs) and XGBoost, have demonstrated their remarkable accuracy in detecting early DFU (e.g., via thermography), predicting ulcer healing, and stratifying amputation risks. The authors also discuss challenges of ML, including data quality and model interpretability, and propose the potential solutions like SHAP (SHapley Additive exPlanations) to elucidate model decision-making processes. With ongoing technological advancements, the application of ML presents unprecedented opportunities to redefine the diagnostic and therapeutic strategies of diabetic foot care.

Furthermore, it has been predicted that nearly 50% of patients with DFU suffer from foot infections (6). Boey et al. present a compelling case report on the use of transtibial transport (TTT) to manage thromboembolic (TE) events following surgical intervention for necrotizing soft tissue infection (NSTI) in a 70-year-old patient with poorly controlled diabetes. TTT is a technique based on distraction osteogenesis, which has been widely applied in ischemic foot disease. The clinical effect of TTT on the resolution of TE events remains unclear, which needs more investigations.

This editorial integrates cutting-edge findings focusing on diagnostic and therapeutic strategies for DFU. Original research and review articles published in this Research Topic provide new perspectives on treatment trends for DFU. We sincerely acknowledge the collaborative efforts of all contributors and reviewers, which have facilitated innovation within the field. Looking ahead, we are committed to translating these research outcomes into patient-centered practice protocols to improve clinical outcomes.

Author contributions

SS: Writing – original draft, Validation, Conceptualization, Writing – review & editing. XR: Supervision, Conceptualization, Writing – review & editing. JB: Validation, Writing – review & editing, Methodology, Supervision.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. van Dieren S, Beulens JW, van der Schouw WT, Grobbee DE, and Neal B. The global burden of diabetes and its complications: an emerging pandemic. Eur J Cardiovasc Prev Rehabil. (2010) 17 Suppl 1:S3–8. doi: 10.1097/01.hjr.0000368191.86614.5a

PubMed Abstract | Crossref Full Text | Google Scholar

2. Fortington LV, Geertzen JHB, van Netten JJ, Postema K, Rommers GM, and Dijkstra PU. Short and long term mortality rates after a lower limb amputation. Eur J Vasc Endovascular Surg. (2013) 46:124–31. doi: 10.1016/j.ejvs.2013.03.024

PubMed Abstract | Crossref Full Text | Google Scholar

3. Nakamura Y, Ishikawa H, Kawai K, Tabata Y, and Suzuki S. Enhanced wound healing by topical administration of mesenchymal stem cells transfected with stromal cell-derived factor-1. Biomaterials. (2013) 34:9393–400. doi: 10.1016/j.biomaterials.2013.08.053

PubMed Abstract | Crossref Full Text | Google Scholar

4. Jiang D, Singh K, Muschhammer J, Schatz S, Sindrilaru A, Makrantonaki E, et al. MSCs rescue impaired wound healing in a murine LAD1 model by adaptive responses to low TGF-β1 levels. EMBO Rep. (2020) 21:e49115. doi: 10.15252/embr.201949115

PubMed Abstract | Crossref Full Text | Google Scholar

5. Gardeazabal L and Izeta A. Elastin and collagen fibres in cutaneous wound healing. Exp Dermatol. (2024) 33:e15052. doi: 10.1111/exd.15052

PubMed Abstract | Crossref Full Text | Google Scholar

6. Hurlow JJ, Humphreys GJ, Bowling FL, and McBain AJ. Diabetic foot infection: A critical complication. Int Wound J. (2018) 15:814–21. doi: 10.1111/iwj.12932

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: mesenchymal stem cells, non-coding RNAs, diabetic foot infection, diabetic foot ulcer, fibrous proteins, machine learning, transtibial transport

Citation: Shao S, Boey J and Ran X (2025) Editorial: Diabetic wound: multifaceted mechanisms and future of diabetic wound healing, volume II. Front. Endocrinol. 16:1650648. doi: 10.3389/fendo.2025.1650648

Received: 20 June 2025; Accepted: 30 June 2025;
Published: 11 July 2025.

Edited and Reviewed by:

Guy A. Rutter, Imperial College London, United Kingdom

Copyright © 2025 Shao, Boey and Ran. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Xingwu Ran, cmFueGluZ3d1QDE2My5jb20=; Johnson Boey, Sm9obnNvbmJjZUBnbWFpbC5jb20=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.