Evidence map›Paper›PMID 42781429›Full record

ReviewBioactive materials2027

Antifibrotic hydrogel strategies for scarless tissue regeneration: mechanisms, design, and application.

Shuangli Zhu, Ying Shi, Haoran Wang, Lei Feng, Yuhui Lu, Xinghui Si, Qiuyue Ma, Liangcan He, Shaoqin Liu

Abstract readReview
In one paragraph

Review in Bioactive materials, 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Shuangli ZhuSchool of Medicine and Health, MOE Key Laboratory of Micro-systems and Micro-structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.
Ying ShiSchool of Medicine and Health, MOE Key Laboratory of Micro-systems and Micro-structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.
Haoran WangSchool of Medicine and Health, MOE Key Laboratory of Micro-systems and Micro-structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.
Lei FengState Key Laboratory of Woody Oil Resources Utilization, Northeast Forestry University, Harbin, 150040, China.
Yuhui LuSchool of Medicine and Health, MOE Key Laboratory of Micro-systems and Micro-structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.
Xinghui SiSchool of Medicine and Health, MOE Key Laboratory of Micro-systems and Micro-structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.
Qiuyue MaSchool of Medicine and Health, MOE Key Laboratory of Micro-systems and Micro-structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.
Liangcan HeSchool of Medicine and Health, MOE Key Laboratory of Micro-systems and Micro-structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.
Shaoqin LiuSchool of Medicine and Health, MOE Key Laboratory of Micro-systems and Micro-structures Manufacturing, Harbin Institute of Technology, Harbin, 150080, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue repair is a highly coordinated process, yet dysregulated fibrosis often diverts healing toward scar formation, resulting in permanent structural and functional impairment. Achieving scarless regeneration requires precise modulation of the wound microenvironment to support functional tissue reconstruction. Hydrogels, owing to their biocompatibility, tunable mechanics, and controllable delivery capabilities, have emerged as promising platforms for regenerative therapy. Recent multifunctional hydrogels can regulate tissue repair through microstructural engineering, mechanical modulation, immune regulation, pro-angiogenic stimulation, and dynamic extracellular matrix remodeling, thereby suppressing fibrotic progression. However, current reviews mainly focus on accelerating wound closure and lack systematic discussion of antifibrotic hydrogel design across different tissues. In this review, we summarize the key mechanisms underlying scar formation and propose design principles for hydrogel-mediated scarless regeneration. We further highlight recent advances in multiple tissues, including skin, tendon, cornea, urethra, nerve, endometrium, liver, myocardium, emphasizing both shared principles and tissue-specific requirements. Finally, we discuss translational challenges and future opportunities, particularly AI-driven hydrogel design for functional regeneration.

Indexed as

AI-Driven hydrogel designAntifibrotic hydrogelsFibrosis modulationScarless tissue regeneration

Identifiers

PMID42781429
PMCPMC13599580

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.