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DOI 10.1007/s10528-026-11338-w

Медицинская библиотека · Biochemical genetics · 2026

The Impact of NEAT1 on Inflammatory Responses and Processes in Arthropathic Diseases: Latest Findings and Perspectives.

Mohammad Suleiman Ibrahim, Saleh Raed Obaid, Owida Hamza Abu, Al-Khafaji Zahraa Abbas, Varma Pooja, Vasudevan Asokan, Kadhum Wesam R, Al-Tameemi Ahmed Read, Mustafa Yasser Fakri, Ansari Shakeel Ahmed

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Аннотация

Arthropathies are joint-related disorders with diverse etiologies but standard clinical and radiographic features. There is growing evidence that long non-coding RNAs (lncRNAs) play a crucial role in regulating the development and progression of certain diseases. Nuclear-enriched abundant transcript 1 (NEAT1) is one of these lncRNAs. It is common and helps control transcription and epigenetics, especially during inflammation. This narrative review presents current data on NEAT1's role in inflammation and its contribution to the development of arthropathies, including psoriasis, rheumatoid arthritis, osteoarthritis, SLE, Behçet's disease, and hemophilic arthropathy. The research demonstrated that NEAT1 regulates immune cell activity, inflammasome formation, and inflammatory signaling pathways through interactions with miRNAs and transcriptional regulators. The activity, progression, and response to treatment of the disease are all linked to its dysregulated expression. In conclusion, NEAT1 appears to be a significant regulator of inflammation and joint disease, potentially serving as both a therapeutic target and a biomarker for joint-related disorders. More mechanistic and translational studies are needed to better understand how it works and how it might be used in medicine.

Для цитирования: Mohammad Suleiman Ibrahim, Saleh Raed Obaid, Owida Hamza Abu, Al-Khafaji Zahraa Abbas, Varma Pooja, Vasudevan Asokan, Kadhum Wesam R, Al-Tameemi Ahmed Read, Mustafa Yasser Fakri, Ansari Shakeel Ahmed. The Impact of NEAT1 on Inflammatory Responses and Processes in Arthropathic Diseases: Latest Findings and Perspectives.. Biochemical genetics. 2026. DOI: 10.1007/s10528-026-11338-w.

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