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Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers
Published on: March 1, 2024
Non-coding RNAs as biomarkers and therapeutic targets in pancreatic cancer: Clinical implications and translational
María Carretero-Fernández1, Lucía Ruíz-Durán2, Pinar Uysal-Onganer3
1Genomic Oncology Area, GENYO. Centre for Genomics and Oncological Research: Pfizer / University of Granada / Andalusian Regional Government, PTS, Granada, Spain; Instituto de Investigación Biosanataria IBs.Granada, Granada, Spain; Department of Biochemistry and Molecular Biology I, University of Granada, Granada, Spain.
Abstract:
Pancreatic cancer remains one of the most lethal malignancies, largely due to late diagnosis, marked tumor heterogeneity, and profound resistance to therapy. Beyond recurrent alterations in protein-coding genes, growing evidence identifies non-coding RNAs (ncRNAs) as key regulators of pancreatic cancer biology and promising tools for clinical translation, particularly in pancreatic ductal adenocarcinoma (PDAC). ncRNAs, including microRNAs, long non-coding RNAs (lncRNAs), circular RNAs (circRNAs), and emerging short RNA species such as small nucleolar RNAs, PIWI-interacting RNAs, and tRNA-derived fragments, modulate gene expression through transcriptional, post-transcriptional, and epigenetic mechanisms. This review synthesizes current knowledge on ncRNA dysregulation across pancreatic cancer entities and highlights their roles in tumor initiation, proliferation, epithelial-mesenchymal transition, invasion, metastatic dissemination, immune evasion, and resistance to chemotherapy and targeted therapies. Beyond tumor-intrinsic effects, ncRNAs actively shape the tumor microenvironment by regulating stromal activation, fibrosis, metabolic adaptation, hypoxia responses, and intercellular communication via extracellular vesicles. Importantly, ncRNAs are emerging as minimally invasive biomarkers for early detection, risk stratification, prognosis, and treatment monitoring. Circulating and extracellular vesicle-associated ncRNAs show particular promise for improving diagnostic accuracy and guiding therapeutic decision-making. In parallel, therapeutic strategies targeting ncRNA pathways, including miRNA mimics, antisense oligonucleotides, RNA interference technologies, and advanced delivery systems, are advancing toward clinical application. Key barriers to clinical implementation include assay standardization, delivery specificity, off-target effects, and the need for large-scale prospective validation. Together, ncRNAs represent central regulators of pancreatic cancer pathobiology and hold significant potential to enable biomarker-driven patient stratification and RNA-based precision therapies.
Insights
Non-coding RNAs (ncRNAs) are crucial in pancreatic cancer, influencing tumor growth, spread, and treatment resistance. They also serve as promising biomarkers for early detection and therapeutic targets in pancreatic ductal adenocarcinoma (PDAC).
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Pancreatic cancer is highly lethal due to late diagnosis, heterogeneity, and therapy resistance.
- Non-coding RNAs (ncRNAs) are increasingly recognized as key regulators in pancreatic cancer biology, especially pancreatic ductal adenocarcinoma (PDAC).
- ncRNAs encompass microRNAs, long non-coding RNAs (lncRNAs), circular RNAs (circRNAs), and other small RNA species.
Purpose of the Study:
- To review current knowledge on ncRNA dysregulation in pancreatic cancer.
- To highlight ncRNAs' roles in tumor initiation, progression, immune evasion, and therapy resistance.
- To explore ncRNAs as biomarkers and therapeutic targets for pancreatic cancer.
Main Methods:
- Literature review synthesizing current research on ncRNAs in pancreatic cancer.
- Analysis of ncRNA involvement in tumor-intrinsic processes and the tumor microenvironment.
- Evaluation of ncRNAs as diagnostic, prognostic, and predictive biomarkers.
Main Results:
- ncRNAs regulate gene expression via transcriptional, post-transcriptional, and epigenetic mechanisms.
- Dysregulated ncRNAs are implicated in tumor initiation, proliferation, invasion, metastasis, immune evasion, and treatment resistance.
- ncRNAs modulate the tumor microenvironment, including stromal activation and intercellular communication.
- Circulating and extracellular vesicle-associated ncRNAs show potential as minimally invasive biomarkers.
- ncRNA-targeting therapies are advancing, with challenges in delivery and specificity.
Conclusions:
- ncRNAs are central regulators of pancreatic cancer pathobiology.
- ncRNAs hold significant potential for biomarker-driven patient stratification and precision therapies.
- Further validation and standardization are needed for clinical implementation of ncRNA-based strategies.
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