Evidence map›Paper›PMID 42601565›Full record

ReviewCell biochemistry and biophysics2026

Secretome Derived from Umbilical Cord Mesenchymal Stem Cells as a Therapeutic Approach for Osteoarthritis: Insights from In Vitro, In Vivo, and Clinical Evidence.

Wahyu Widowati, Lydia Lydia, Gabriella Rumayauw J, Monica Permatasari Wijaya, Megan Caroline S S, Jose Hady Putera, Merisa Noviliany Rachmad, Rizal Aziz, Rizky Pratama, Elnaz Zand

Abstract readReview
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In one paragraph

Review in Cell biochemistry and biophysics, 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

10 authors.

Wahyu WidowatiMaster Program of Skin Aging and Aesthetic Medicine, Faculty of Medicine, Maranatha Christian University, Bandung, West Java, 40164, Indonesia. wahyu_w60@yahoo.com.
Lydia LydiaMaster Program of Skin Aging and Aesthetic Medicine, Faculty of Medicine, Maranatha Christian University, Bandung, West Java, 40164, Indonesia.
Gabriella Rumayauw JMaster Program of Skin Aging and Aesthetic Medicine, Faculty of Medicine, Maranatha Christian University, Bandung, West Java, 40164, Indonesia.
Monica Permatasari WijayaMaster Program of Skin Aging and Aesthetic Medicine, Faculty of Medicine, Maranatha Christian University, Bandung, West Java, 40164, Indonesia.
Megan Caroline S SMaster Program of Skin Aging and Aesthetic Medicine, Faculty of Medicine, Maranatha Christian University, Bandung, West Java, 40164, Indonesia.
Jose Hady PuteraMaster Program of Skin Aging and Aesthetic Medicine, Faculty of Medicine, Maranatha Christian University, Bandung, West Java, 40164, Indonesia.
Merisa Noviliany RachmadMaster Program of Skin Aging and Aesthetic Medicine, Faculty of Medicine, Maranatha Christian University, Bandung, West Java, 40164, Indonesia.
Rizal AzizBiomedical Engineering, Department of Electrical Engineering, Faculty of Engineering, Universitas Indonesia, Depok, Indonesia.
Rizky PratamaBiomolecular and Biomedical Research Center, Aretha Medika Utama, Bandung, Indonesia.
Elnaz ZandDepartment of Electronic Engineering and Information Science, University of Science and Technology of China, Hefei, Anhui, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is a chronic degenerative joint disorder characterized by articular cartilage deterioration, synovial inflammation, and progressive loss of joint function. Current treatments predominantly address symptoms without modifying structural disease progression, highlighting the need for disease-modifying strategies. Mesenchymal stem cells (MSCs), particularly umbilical cord-derived MSCs (UC-MSCs), exert therapeutic effects primarily through paracrine mechanisms rather than direct engraftment. The UC-MSCs secretome, comprising soluble bioactive factors and extracellular vesicles, modulates pro-inflammatory signaling, inhibits chondrocyte apoptosis, and promotes cartilage matrix biosynthesis. In vitro studies demonstrate restoration of anabolic chondrocyte phenotype, suppression of catabolic enzymes (MMP-13, ADAMTS-5), and attenuation of NF-κB and MAPK pathway activation. Preclinical models show preservation of cartilage architecture, reduced synovial inflammation, and improved joint function following intra-articular administration. Early clinical investigations report reductions in pain scores and functional improvements with favorable short-term safety profiles, though evidence remains largely derived from MSCs-based rather than secretome-specific interventions. Current findings support the biological plausibility and translational potential of UC-MSCs secretome therapy; however, clinical evidence remains limited and heterogeneous. Adequately powered randomized controlled trials with standardized protocols and extended follow-up are required to establish long-term efficacy and safety.

Indexed as

Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationOsteoarthritisSecretomeUmbilical CordAnimalsChondrocytesHumansCartilage regenerationExtracellular vesiclesOsteoarthritisParacrine signalingSecretomeUmbilical cord mesenchymal stem cells

Identifiers

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.