The Combined Regulation of Long Non-coding RNA and RNA-Binding Proteins in Atherosclerosis

Yuanyuan Ding1, Ruihua Yin1, Shuai Zhang1

  • 1Department of Neurology, The Affiliated Hospital of Qingdao University, Qingdao, China.

Insights

Long non-coding RNAs (lncRNAs) and RNA-binding proteins (RBPs) are key regulators in atherosclerosis. This review details their interactions and roles in the disease, offering new insights into molecular mechanisms.

Area of Science:

  • Cardiovascular Biology
  • Molecular Medicine
  • RNA Biology

Background:

  • Atherosclerosis is a complex cardiovascular disease involving endothelial cells, monocytes/macrophages, and vascular smooth muscle cells.
  • Despite progress, the molecular mechanisms underlying atherosclerosis remain incompletely understood, highlighting the need for further research.
  • Long non-coding RNAs (lncRNAs) and RNA-binding proteins (RBPs) have emerged as critical regulators of cellular functions relevant to atherosclerosis.

Purpose of the Study:

  • To review the significant roles of lncRNAs and RBPs in the pathogenesis of atherosclerosis.
  • To elucidate the functional interplay between lncRNAs and RBPs in the context of this disease.
  • To present novel interaction models illustrating how lncRNAs and RBPs coordinate cellular functions in atherosclerosis.

Main Methods:

  • Comprehensive literature review of studies investigating lncRNAs and RBPs in atherosclerosis.
  • Analysis of existing data on lncRNA-RBP interactions and their functional consequences.
  • Synthesis of information to propose new models of lncRNA-RBP complex formation and function.

Main Results:

  • lncRNAs and RBPs significantly influence key cellular processes in atherosclerosis, including inflammation, lipid metabolism, and cell proliferation.
  • Specific interactions between lncRNAs and RBPs are crucial for modulating gene expression and cellular behavior in atherosclerotic lesions.
  • Evidence suggests that lncRNA-RBP complexes act as critical hubs for integrating molecular signals in the atherosclerotic microenvironment.

Conclusions:

  • lncRNAs and RBPs are integral components of the molecular machinery driving atherosclerosis.
  • Understanding lncRNA-RBP interactions provides a deeper insight into atherosclerosis pathogenesis.
  • Targeting lncRNA-RBP interactions may offer novel therapeutic strategies for atherosclerosis.

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