4.7 Review

Exploring microRNAs in diabetic chronic cutaneous ulcers: Regulatory mechanisms and therapeutic potential

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 177, Issue 18, Pages 4077-4095

Publisher

WILEY
DOI: 10.1111/bph.15139

Keywords

Diabetic chronic cutaneous ulcers; microRNAs; NF-kappa B signaling pathway; PI3K/AKT/mTOR signaling pathway; TGF-beta/Smad signaling pathway Wnt/beta-catenin signaling pathway

Funding

  1. Guizhou Provincial Natural Science Foundation [QKH-J-2020-1Z070]
  2. Special Funding for Postdoctoral Research Projects in Chongqing [Xm2019061]
  3. Science and Technology Department Foundation of Guizhou Province of China [QKHPTRC[2019]5657]
  4. Guizhou Provincial Administration of Traditional Chinese Medicine Funding [QZYY2017-080]
  5. 2011 Collaborative Inovation Center of Guizhou Traditional Chinese Medicine and Ethnic Medicine [2012-311]
  6. Zunyi 15851 Talents Elite Project Funding [2015019]
  7. National Natural Science Foundation of China [81560673, 81560712, 81960741]

Ask authors/readers for more resources

Diabetic chronic cutaneous ulcers (DCU) are one of the serious complications of diabetes mellitus, occurring mainly in diabetic patients with peripheral neuropathy. Recent studies have indicated that microRNAs (miRNAs/miRs) and their target genes are essential regulators of cell physiology and pathology including biological processes that are involved in the regulation of diabetes and diabetes-related microvascular complications. in vivo and in vitro models have revealed that the expression of some miRNAs can be regulated in the inflammatory response, cell proliferation, and wound remodelling of DCU. Nevertheless, the potential application of miRNAs to clinical use is still limited. Here, we provide a contemporary overview of the miRNAs as well as their associated target genes and pathways (including Wnt/beta-catenin, NF-kappa B, TGF-beta/Smad, and PI3K/AKT/mTOR) related to DCU healing. We also summarize the current development of drugs for DCU treatment and discuss the therapeutic challenges of DCU treatment and its future research directions.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available