ReviewFASEB bioAdvances2026
Retrotransposons in Bone and Joint Diseases.
Review in FASEB bioAdvances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Retrotransposons, including non-LTR elements such as LINEs and viral-derived endogenous retroviruses (ERVs), have long been dismissed as "junk DNA" and thought to be biochemically inert. However, emerging evidence suggests that the erosion of epigenetic control during aging and pathological states can lead to the awakening of these dormant genetic elements. Although the role of ERVs in cancer and neurodegeneration is increasingly recognized, their impact on musculoskeletal health has received little attention. This perspective review synthesizes recent and previous findings linking retrotransposon reactivation (particularly ERVs) to osteoarthritis (OA), rheumatoid arthritis (RA), and potentially osteoporosis. We discuss the epigenetic mechanisms that typically silence ERVs in musculoskeletal tissues, how these mechanisms fail in disease, and how the resulting reactivation leads to viral and molecular mimicry. These processes trigger both innate and adaptive immune responses, as well as cellular senescence. Finally, we highlight the therapeutic potential of targeting retrotransposon dysregulation, including its encoded proteins and nucleic acid-sensing pathways to treat chronic bone and joint disorders.
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Registered trials
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.