4.8 Review

Inflammatory Immune-Associated eRNA: Mechanisms, Functions and Therapeutic Prospects

期刊

FRONTIERS IN IMMUNOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.849451

关键词

eRNA; immune inflammatory; enhancer transcription events; cancers; therapeutic prospects

资金

  1. National Natural Science Foundation of China [81872089, 81370849, 81672551]
  2. Six talent peaks project in Jiangsu Province
  3. Jiangsu Provincial Medical Innovation Team [CXTDA2017025]
  4. National Key Research and Development Program of China [SQ2017YFSF090096]
  5. Innovative Team of Jiangsu Provincial [2017ZXKJQWO7]

向作者/读者索取更多资源

This review summarizes the roles and regulatory mechanisms of functional enhancers and enhancer RNAs (eRNAs) in inflammatory immune cells, non-inflammatory immune cells, inflammatory immune diseases, and tumors, and explores the potential therapeutic effects of enhancer inhibitors affecting eRNA production for diseases with inflammatory immune responses.
The rapid development of multiple high-throughput sequencing technologies has made it possible to explore the critical roles and mechanisms of functional enhancers and enhancer RNAs (eRNAs). The inflammatory immune response, as a fundamental pathological process in infectious diseases, cancers and immune disorders, coordinates the balance between the internal and external environment of the organism. It has been shown that both active enhancers and intranuclear eRNAs are preferentially expressed over inflammation-related genes in response to inflammatory stimuli, suggesting that enhancer transcription events and their products influence the expression and function of inflammatory genes. Therefore, in this review, we summarize and discuss the relevant inflammatory roles and regulatory mechanisms of eRNAs in inflammatory immune cells, non-inflammatory immune cells, inflammatory immune diseases and tumors, and explore the potential therapeutic effects of enhancer inhibitors affecting eRNA production for diseases with inflammatory immune responses.

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