Evidence map›Paper›PMID 39826569›Full record

ReviewPharmacology & therapeutics2025

Unfolded protein responses: Dynamic machinery in wound healing.

Morgan Minjares, Pattaraporn Thepsuwan, Kezhong Zhang, Jie-Mei Wang

Abstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
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  5. Article
  6. 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

4 authors.

Morgan MinjaresDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, USA.
Pattaraporn ThepsuwanCenters for Molecular Medicine and Genetics, Wayne State University, USA.
Kezhong ZhangCenters for Molecular Medicine and Genetics, Wayne State University, USA; Department of Biochemistry, Microbiology, and Immunology, Wayne State University, Detroit, MI, USA. Electronic address: kzhang@med.wayne.edu.
Jie-Mei WangDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, USA; Centers for Molecular Medicine and Genetics, Wayne State University, USA; Karmanos Cancer Institute, Detroit, MI, USA. Electronic address: jiemei.wang@wayne.edu.

Funding

Regulation of Hepatic Steatosis by an ER Stress-Inducible Transcription Factor CRR01DK090313 · NIDDK · WAYNE STATE UNIVERSITY · PI Kezhong Zhang · 2011 to 2026
$5.0M
Novel Role of Hepatic SEL1L-HRD1 ERAD in FGF21 Gene TranscriptionR01DK120330 · NIDDK · UNIVERSITY OF VIRGINIA · PI Deyu Fang, Ling Qi · 2018 to 2026
$4.9M
Training Modules at Wayne State University to Promote Safe and Inclusive EnvironmentsT32GM139807 · NIGMS · WAYNE STATE UNIVERSITY · PI BRYANT-FRIEDRICH, AMANDA C, CHOW, CHRISTINE S · 2021 to 2025
$2.6M
Targeting SGLTs for liver disease in a rabbit model of cystic fibrosisR01DK134361 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JIE XU, Kezhong Zhang · 2023 to 2026
$2.5M
Regulation of Rhythmic m6A RNA Modification by ER‐associated DegradationR01DK126908 · NIDDK · WAYNE STATE UNIVERSITY · PI FANG, DEYU, ZHANG, KEZHONG · 2021 to 2024
$2.2M
Role of Inositol Requiring Enzyme 1 in Regulating Angiogenesis for Diabetic Wound RepairR01DK109036 · NIDDK · WAYNE STATE UNIVERSITY · PI WANG, JIEMEI · 2016 to 2020
$1.7M
Mechanistic study of Small-molecular Therapy in diabetic Wound HealingR01DK128937 · NIDDK · WAYNE STATE UNIVERSITY · PI WANG, JIEMEI, YI, ZHENGPING · 2021 to 2024
$1.6M
Mitochondrial NAD kinase: function and mechanism in metabolismR01DK132065 · NIDDK · WAYNE STATE UNIVERSITY · PI ZHANG, KEZHONG, ZHANG, REN · 2022 to 2025
$1.5M
Alleviating Reactive Carbonyl Species-Induced Progenitor Cell Dysfunction in Diabetic Wound HealingR01DK119222 · NIDDK · WAYNE STATE UNIVERSITY · PI MONKS, TERRENCE J., WANG, JIEMEI · 2019 to 2022
$1.5M
NIDDK NIH HHS R01 DK090313NIDDK NIH HHS R01 DK109036NIDDK NIH HHS R01 DK119222NIDDK NIH HHS R01 DK120330NIDDK NIH HHS R01 DK126908NIDDK NIH HHS R01 DK128937NIDDK NIH HHS R01 DK132065NIDDK NIH HHS R01 DK134361NIGMS NIH HHS T32 GM139807
6 · The paper itself

Abstract

Skin wound healing is a dynamic process consisting of multiple cellular and molecular events that must be tightly coordinated to repair the injured tissue efficiently. The healing pace is decided by the type of injuries, the depth and size of the wounds, and whether wound infections occur. However, aging, comorbidities, genetic factors, hormones, and nutrition also impact healing outcomes. During wound healing, cells undergo robust processes of synthesizing new proteins and degrading multifunctional proteins. This imposes an increasing burden on the endoplasmic reticulum (ER), causing ER stress. Unfolded protein response (UPR) represents a collection of highly conserved stress signaling pathways originated from the ER to maintain protein homeostasis and modulate cell physiology. UPR is known to be beneficial for tissue healing. However, when excessive ER stress exceeds ER's folding potential, UPR pathways trigger cell apoptosis, interrupting tissue regeneration. Understanding how UPR pathways modulate the skin's response to injuries is critical for new interventions toward the control of acute and chronic wounds. Herein, in this review, we focus on the participation of the canonical and noncanonical UPR pathways during different stages of wound healing, summarize the available evidence demonstrating UPR's unique position in balancing homeostasis and pathophysiology of healing tissues, and highlight the understudied areas where therapeutic opportunities may arise.

Indexed as

Unfolded Protein ResponseWound HealingAnimalsEndoplasmic Reticulum StressHumansSignal TransductionSkinEndoplasmic reticulumGene therapyUnfolded protein responseWound healing

Identifiers

PMID39826569
PMCPMC11881203

What OpenQuestion holds

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Registered trials

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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.