Evidence map›Paper›PMID 38338785›Full record

ReviewInternational journal of molecular sciences2024

Exosomal Osteoclast-Derived miRNA in Rheumatoid Arthritis: From Their Pathogenesis in Bone Erosion to New Therapeutic Approaches.

Sandra Pascual-García, Pascual Martínez-Peinado, Carolina Pujalte-Satorre, Alicia Navarro-Sempere, Jorge Esteve-Girbés, Ana B López-Jaén, Juan Javaloyes-Antón, Raúl Cobo-Velacoracho, Francisco J Navarro-Blasco, José M Sempere-Ortells

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
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

12 citing papers in PubMed, 16 citations in OpenAlex.

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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 at 1 institution in 1 country.

Sandra Pascual-GarcíaDepartment of Biotechnology, University of Alicante, 03690 San Vicente del Raspeig, Spain.ORCID 0000-0002-0536-1185
Pascual Martínez-PeinadoDepartment of Biotechnology, University of Alicante, 03690 San Vicente del Raspeig, Spain.ORCID 0000-0003-4370-5468
Carolina Pujalte-SatorreDepartment of Biotechnology, University of Alicante, 03690 San Vicente del Raspeig, Spain.
Alicia Navarro-SempereDepartment of Biotechnology, University of Alicante, 03690 San Vicente del Raspeig, Spain.
Jorge Esteve-GirbésDepartment of Legal Studies of the State, University of Alicante, 03690 San Vicente del Raspeig, Spain.
Ana B López-JaénDepartment of Biotechnology, University of Alicante, 03690 San Vicente del Raspeig, Spain.
Juan Javaloyes-AntónDepartment of Physics, Systems Engineering and Signal Theory, University of Alicante, 03690 San Vicente del Raspeig, Spain.
Raúl Cobo-VelacorachoDepartment of Biotechnology, University of Alicante, 03690 San Vicente del Raspeig, Spain.
Francisco J Navarro-BlascoDepartment of Biotechnology, University of Alicante, 03690 San Vicente del Raspeig, Spain.
José M Sempere-OrtellsDepartment of Biotechnology, University of Alicante, 03690 San Vicente del Raspeig, Spain.
University of Alicante · ES

Funding

Generalitat Valenciana CIGE/2021/162University of Alicante GRE21-17
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is an autoimmune disease that causes inflammation, pain, and ultimately, bone erosion of the joints. The causes of this disease are multifactorial, including genetic factors, such as the presence of the human leukocyte antigen (HLA)-DRB1*04 variant, alterations in the microbiota, or immune factors including increased cytotoxic T lymphocytes (CTLs), neutrophils, or elevated M1 macrophages which, taken together, produce high levels of pro-inflammatory cytokines. In this review, we focused on the function exerted by osteoclasts on osteoblasts and other osteoclasts by means of the release of exosomal microRNAs (miRNAs). Based on a thorough revision, we classified these molecules into three categories according to their function: osteoclast inhibitors (miR-23a, miR-29b, and miR-214), osteoblast inhibitors (miR-22-3p, miR-26a, miR-27a, miR-29a, miR-125b, and miR-146a), and osteoblast enhancers (miR-20a, miR-34a, miR-96, miR-106a, miR-142, miR-199a, miR-324, and miR-486b). Finally, we analyzed potential therapeutic targets of these exosomal miRNAs, such as the use of antagomiRs, blockmiRs, agomiRs and competitive endogenous RNAs (ceRNAs), which are already being tested in murine and ex vivo models of RA. These strategies might have an important role in reestablishing the regulation of osteoclast and osteoblast differentiation making progress in the development of personalized medicine.

Indexed as

Arthritis, RheumatoidMicroRNAsAnimalsAntagomirsHumansMacrophagesMiceOsteoblastsOsteoclastsAntagomirsMicroRNAsMIRN214 microRNA, humanMIRN324 microRNA, humanexosomesmiRNAsosteoblastosteoclastrheumatoid arthritis

Identifiers

PMID38338785
PMCPMC10855630
OpenAlexW4391219742

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.