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.

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.