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Interplay between Reactive oxygen Species and MicroRNAs in Cancer
1Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, USA.
Abstract:
Since both reactive oxygen species (ROS) production and microRNAs expression signature have been associated with tumor development, progression, metastasis and therapeutic response, it is important to understand the crosstalk between ROS and microRNAs. Indeed, growing evidence suggests a reciprocal connection between ROS signaling and microRNAs pathway, resulting in diverse biological effects in cancer cells. In this mini review, we discussed the ROS-responsive microRNAs that have implications in cancer and the possible mechanisms in which ROS regulate microRNAs. We also highlighted the microRNAs which are able to modify cellular ROS homeostasis during tumorigenesis, their biological targets and subsequent functions. As the use of antioxidants is limited due to the diverse or even opposing roles of ROS signaling in cancer, the discovery of ROS-responsive microRNAs provides a potential new strategy to specifically overcome ROS-mediated tumor progression or benefit from ROS-induced apoptosis.
Insights
Reactive oxygen species (ROS) and microRNAs are key in cancer. This review explores their reciprocal relationship, revealing ROS-responsive microRNAs as potential cancer therapeutics targeting tumor progression and apoptosis.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Reactive oxygen species (ROS) production and microRNA expression are implicated in tumor development, progression, metastasis, and therapeutic response.
- A reciprocal connection exists between ROS signaling and microRNA pathways, influencing cancer cell biology.
- Understanding this crosstalk is crucial for cancer research and treatment strategies.
Purpose of the Study:
- To review ROS-responsive microRNAs relevant to cancer.
- To elucidate mechanisms by which ROS regulate microRNAs.
- To highlight microRNAs that modulate cellular ROS homeostasis and their functions in tumorigenesis.
Main Methods:
- Literature review of studies investigating ROS and microRNAs in cancer.
- Analysis of mechanisms linking ROS signaling to microRNA regulation.
- Identification of microRNAs affecting ROS homeostasis and their biological targets.
Main Results:
- Several microRNAs are responsive to ROS and play roles in cancer.
- ROS can regulate microRNA expression through various mechanisms.
- Certain microRNAs can alter cellular ROS levels, impacting tumorigenesis.
Conclusions:
- The interplay between ROS and microRNAs offers novel therapeutic avenues in oncology.
- Targeting ROS-responsive microRNAs may provide strategies to combat ROS-mediated tumor progression.
- Exploiting this relationship could lead to new approaches for inducing ROS-dependent apoptosis in cancer cells.
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