Evidence map›Paper›PMID 41877659›Full record

ArticleInternational endodontic journal2026

Novel Midkine-Derived Peptide Promotes Reparative Dentine Formation via DDIT4/mTOR Pathway-Mediated Activation of Autophagy.

Shuwei Qiao, Jiawen Wang, Hamed Alshawwa, Xinying Zou, Chao Si, Yuyang Li, Xi He, Song Zhu

Abstract read
In one paragraph

Article in International endodontic journal, 2026. 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

8 authors.

Shuwei QiaoJilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, School and Hospital of Stomatology, Jilin University, Changchun, Jilin, China.ORCID https://orcid.org/0000-0001-9256-6770
Jiawen WangJilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, School and Hospital of Stomatology, Jilin University, Changchun, Jilin, China.
Hamed AlshawwaJilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, School and Hospital of Stomatology, Jilin University, Changchun, Jilin, China.ORCID https://orcid.org/0000-0001-9069-6758
Xinying ZouJilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, School and Hospital of Stomatology, Jilin University, Changchun, Jilin, China.
Chao SiJilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, School and Hospital of Stomatology, Jilin University, Changchun, Jilin, China.
Yuyang LiDepartment of Prosthodontics, Nanjing Stomatological Hospital, Affiliated Hospital of Medical School, Research Institute of Stomatology, Nanjing University, Nanjing, Jiangsu, China.
Xi HeHospital of Stomatology, Jilin University, Changchun, Jilin, China.ORCID https://orcid.org/0000-0003-1478-0215
Song ZhuHospital of Stomatology, Jilin University, Changchun, Jilin, China.ORCID https://orcid.org/0000-0001-6935-9490

Funding

Department of Science and Technology of Jilin Province 20250203025SF
6 · The paper itself

Abstract

aimMidkine (MK) protein plays a critical regulatory role in tooth development and odontogenic differentiation, and has been shown to significantly promote reparative dentine formation. However, the direct application of recombinant MK protein as a pulp capping material presents clinical challenges and may increase medical costs. In contrast, peptides offer a cost-effective and feasible alternative by overcoming many of the limitations associated with full-length proteins. This study aimed to develop a novel MK-derived peptide for use in vital pulp therapy (VPT). METHODOLOGY: The human MK protein sequence was appropriately cleaved, resulting in the generation of multiple MK-derived peptides. The peptide with the highest mineralisation potential was identified through quantitative polymerase chain reaction (qPCR) and alizarin red S (ARS) staining. Cell proliferation, live/dead cell staining and apoptosis assays were conducted to evaluate the in vitro biosafety of MK-derived peptide. The optimal concentration of MK-derived peptide for promoting cell migration and odontogenic differentiation was determined using cell migration assays, qPCR, Western blotting, alkaline phosphatase staining and ARS staining. RNA sequencing, bioinformatics analysis, transmission electron microscopy and siRNA were used to explore the potential mechanism by which MK-derived peptide promotes odontogenesis. A rat pulp capping model was established, and in vivo evaluation was conducted through Micro-CT, H&E, Masson and immunohistochemical staining.

resultsFollowing appropriate cleavage of the human MK protein, a total of 15 peptides were generated, among which MK-12 (KARYNAQCQETI) exhibited the highest mineralisation potential. MK-12 demonstrated favourable in vitro biocompatibility at concentrations below 200 μg/mL, with the optimal effect on promoting cell migration and odontogenic differentiation observed at 100 μg/mL. RNA-sequencing and functional analyses revealed that MK-12 was closely associated with autophagy and mammalian target of rapamycin (mTOR) signalling pathways. Subsequent experiments demonstrated that MK-12 modulates the mTOR pathway and autophagy by upregulating the expression of DNA damage-inducible transcript 4 (DDIT4). In vivo studies confirmed that MK-12 effectively promoted the formation of reparative dentine and exhibited favourable biocompatibility.

conclusionMK-12, a peptide derived from midkine, was found to promote reparative dentine formation via DDIT4/mTOR pathway-mediated activation of autophagy, thereby providing a mechanistic basis for its potential clinical application in VPT.

Indexed as

AutophagyDentin, SecondaryMidkinePeptidesTOR Serine-Threonine KinasesTranscription FactorsAnimalsCell DifferentiationCell MovementCell ProliferationHumansRatsRats, Sprague-DawleySignal TransductionMidkinePeptidesTOR Serine-Threonine KinasesTranscription Factorsanimal modeldental pulp stem cellsdentinogenesismidkinepeptidespulp capping materialreparative dentine

Identifiers

PMID41877659
PMCPMC13373034

What Socratic 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 Socratic graph.