The crosstalk between reactive oxygen species and noncoding RNAs: from cancer code to drug role

Mol Cancer. 2022 Jan 26;21(1):30. doi: 10.1186/s12943-021-01488-3.

Abstract

Oxidative stress (OS), characterized by the excessive accumulation of reactive oxygen species (ROS), is an emerging hallmark of cancer. Tumorigenesis and development driven by ROS require an aberrant redox homeostasis, that activates onco-signaling and avoids ROS-induced programmed death by orchestrating antioxidant systems. These processes are revealed to closely associate with noncoding RNAs (ncRNAs). On the basis of the available evidence, ncRNAs have been widely identified as multifarious modulators with the involvement of several key redox sensing pathways, such as NF-κB and Nrf2 signaling, therefore potentially becoming effective targets for cancer therapy. Furthermore, the vast majority of ncRNAs with property of easy detected in fluid samples (e.g., blood and urine) facilitate clinicians to monitor redox homeostasis, indicating a novel method for cancer diagnosis. Herein, focusing on carcinoma initiation, metastasis and chemoradiotherapy resistance, we aimed to discuss the ncRNAs-ROS network involved in cancer progression, and the potential clinical application as biomarkers and therapeutic targets.

Keywords: Cancer diagnosis; Cancer therapy; Noncoding RNAs; Oxidative stress; Reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism
  • Combined Modality Therapy
  • Disease Management
  • Disease Progression
  • Disease Susceptibility
  • Gene Expression Regulation, Neoplastic* / drug effects
  • Humans
  • Neoplasm Metastasis
  • Neoplasms / diagnosis
  • Neoplasms / drug therapy
  • Neoplasms / genetics*
  • Neoplasms / metabolism*
  • Oxidative Stress
  • Prognosis
  • RNA, Untranslated / genetics*
  • Reactive Oxygen Species / metabolism*
  • Signal Transduction* / drug effects
  • Treatment Outcome

Substances

  • RNA, Untranslated
  • Reactive Oxygen Species