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Updated: Jan 2, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as A Novel Detection and Quantification Method
Published on: October 7, 2025
microRNAs Tune Oxidative Stress in Cancer Therapeutic Tolerance and Resistance
1Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, 6900 Lake Nona Blvd, Orlando, FL 32827, USA.
Abstract:
Relapsed disease following first-line therapy remains one of the central problems in cancer management, including chemotherapy, radiotherapy, growth factor receptor-based targeted therapy, and immune checkpoint-based immunotherapy. Cancer cells develop therapeutic resistance through both intrinsic and extrinsic mechanisms including cellular heterogeneity, drug tolerance, bypassing alternative signaling pathways, as well as the acquisition of new genetic mutations. Reactive oxygen species (ROSs) are byproducts originated from cellular oxidative metabolism. Recent discoveries have shown that a disabled antioxidant program leads to therapeutic resistance in several types of cancers. ROSs are finely tuned by dysregulated microRNAs, and vice versa. However, mechanisms of a crosstalk between ROSs and microRNAs in regulating therapeutic resistance are not clear. Here, we summarize how the microRNA-ROS network modulates cancer therapeutic tolerance and resistance and direct new vulnerable targets against drug tolerance and resistance for future applications.
Insights
Cancer cells develop resistance to treatments like chemotherapy and immunotherapy through complex mechanisms. This study explores the crucial interplay between microRNAs and reactive oxygen species (ROSs) in overcoming cancer drug resistance.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Therapeutic resistance is a major challenge in cancer treatment, impacting chemotherapy, targeted therapy, and immunotherapy.
- Cancer cells employ intrinsic and extrinsic mechanisms to evade treatment, including genetic mutations and pathway alterations.
- Reactive oxygen species (ROSs), byproducts of metabolism, are increasingly recognized for their role in cancer development and treatment resistance, particularly when antioxidant defenses are compromised.
Purpose of the Study:
- To elucidate the mechanisms by which the microRNA-ROS network influences cancer therapeutic tolerance and resistance.
- To identify novel therapeutic targets within the microRNA-ROS axis for overcoming drug resistance.
Main Methods:
- Review and synthesis of current literature on microRNA regulation, ROS metabolism, and cancer therapeutic resistance.
- Analysis of the crosstalk between microRNAs and ROSs in the context of cancer cell survival and treatment evasion.
Main Results:
- Dysregulated microRNAs fine-tune ROS levels, contributing to cancer cells' ability to withstand therapy.
- The intricate network between microRNAs and ROSs plays a significant role in both cancer cell tolerance and the development of resistance.
- Specific microRNA-ROS interactions represent potential vulnerabilities in resistant cancer cells.
Conclusions:
- The microRNA-ROS network is a critical modulator of cancer therapeutic resistance.
- Targeting the microRNA-ROS crosstalk offers promising strategies for developing novel therapies to overcome drug resistance in various cancers.
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