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Published on: May 30, 2025
Noncoding RNAs in DNA Damage Response: Opportunities for Cancer Therapeutics
Wani Arjumand1, Asia Asiaf2, Shiekh Tanveer Ahmad3
1Robson DNA Science Centre, Arnie Charbonneau Cancer Institute, Cumming School of Medicine, 2A32 HRIC, University of Calgary, 3330 Hospital Drive NW, Calgary, AB, T2N4N1, Canada.
Abstract:
DNA repair machinery preserves genomic integrity, which is frequently challenged through endogenous and exogenous toxic insults, and any sort of repair machinery malfunctioning ultimately manifests in the form of several types of terrible human diseases such as cancers (Hoeijmakers, Nature 411(6835): 366-374, 2001). Noncoding RNAs (ncRNAs) are crucial players of DNA repair machinery in a cell and play a vital role in maintaining genomic stability, which is essential for its survival and normal functioning thus preventing tumorigenesis. To preserve the integrity of the genome, cells initiate a specific cellular response, recognized as DNA damage response (DDR), which includes several distinct DNA repair pathways. These repair pathways permit normal cells to repair DNA damage or induce apoptosis and cell cycle arrest in case the damage is irreparable. Disruption of these pathways in cancer leads to an increase in genomic instability and mutagenesis. Recently, emerging evidence suggests that ncRNAs play a critical role in the regulation of DDR. There is an extensive crosstalk between ncRNAs and the canonical DDR signaling pathway. DDR-induced expression of ncRNAs can provide a regulatory mechanism to accurately control the expression of DNA damage responsive genes in a spatio-temporal manner. DNA damage alters expression of a variety of ncRNAs at multiple levels including transcriptional regulation, post-transcriptional regulation, and RNA degradation and vice versa, wherein ncRNAs can directly regulate cellular processes involved in DDR by altering expression of their targeting genes, with a particular emphasis on microRNAs (miRNAs) and long noncoding RNAs (lncRNAs). Relationship between the defects in the DDR and deregulation of related ncRNAs in human cancers is one of the established, which is growing stronger with the advent of high-throughput sequencing techniques such as next-generation sequencing. Understanding of the mechanisms that explain the association between ncRNAs and DDR/DNA repair pathways will definitely increase our understanding on human tumor biology and on different responses to diverse drugs. Different ncRNAs interact with distinct DDR components and are promising targets for improving the effects to overcome the resistance to conventional chemotherapeutic agents. In this chapter, we will focus the role of ncRNAs in the DNA damage, repair, and cancer.
Insights
Noncoding RNAs (ncRNAs) are vital for DNA repair and genomic stability, preventing diseases like cancer. Their dysregulation is linked to cancer, offering new therapeutic targets for drug resistance.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- Genomic integrity is crucial for cell survival and preventing diseases like cancer.
- DNA damage response (DDR) pathways maintain genomic stability.
- Noncoding RNAs (ncRNAs) are increasingly recognized for their regulatory roles in cellular processes.
Purpose of the Study:
- To explore the critical role of ncRNAs in regulating the DNA damage response (DDR).
- To understand the intricate crosstalk between ncRNAs and DDR pathways.
- To highlight the implications of ncRNA-DDR interactions in cancer biology and therapeutic strategies.
Main Methods:
- Review of existing literature on ncRNAs and DDR.
- Analysis of high-throughput sequencing data (e.g., next-generation sequencing) linking ncRNA deregulation to DDR defects.
- Examination of molecular mechanisms of ncRNA-DDR interactions.
Main Results:
- ncRNAs, particularly microRNAs (miRNAs) and long noncoding RNAs (lncRNAs), are key regulators of DDR.
- DNA damage alters ncRNA expression, and ncRNAs, in turn, modulate DDR gene expression.
- Dysregulation of ncRNAs is associated with DDR defects and genomic instability in cancers.
Conclusions:
- ncRNAs are integral components of the DDR machinery, influencing DNA repair and cellular responses to damage.
- Understanding ncRNA-DDR interactions deepens insights into tumor biology and drug responses.
- Targeting ncRNAs holds promise for overcoming chemoresistance and improving cancer therapy.
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Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...

