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Related Experiment Video

Updated: Jun 27, 2026

Detection of Cell-Free DNA in Blood Plasma Samples of Cancer Patients
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Where Does Liquid Biopsy Add Value in Thyroid Cancer? Biological Rationale, Technological Innovation, and Clinical

María Alonso-Chamorro1, Ainhoa Palacios Mejorada1, Garcilaso Riesco-Eizaguirre1,2

  • 1Molecular Endocrinology Group, Faculty of Medicine, Universidad Francisco de Vitoria, 28223 Madrid, Spain.

Biomedicines
|June 26, 2026
PubMed
Summary

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BRAF V600E in thyroid cancer: navigating prognostic uncertainty and therapeutic opportunity.

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DNA Methylation Dynamics and Prognostic Implications in Metastatic Differentiated Thyroid Cancer.

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Validation of dynamic risk stratification and impact of BRAF in risk assessment of thyroid cancer, a nation-wide multicenter study.

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Liquid biopsy offers promising biomarkers for diverse thyroid cancers. Advances in circulating tumor DNA, microRNAs, extracellular vesicles, and circulating tumor cells aid diagnosis and treatment monitoring.

Area of Science:

  • Oncology
  • Biomarker Discovery
  • Molecular Diagnostics

Background:

  • Thyroid cancer presents diverse subtypes, necessitating minimally invasive biomarkers.
  • Current diagnostic and monitoring methods require improvement for various thyroid cancer types.

Purpose of the Study:

  • To review recent advancements in liquid biopsy techniques for thyroid cancer.
  • To explore various analytes and technologies applicable to thyroid cancer liquid biopsies.
  • To provide a framework for selecting appropriate liquid biopsy analytes based on clinical needs.

Main Methods:

  • Review of circulating tumor DNA (ctDNA) technologies (qPCR/ddPCR, NGS) and strategies (tumor-informed/agnostic).
  • Analysis of circulating microRNAs (miRNAs) in bulk and extracellular vesicle (EV)-enriched samples.
Keywords:
CTCsctDNAextracellular vesicles (EVs)liquid biopsymicroRNAsthyroid cancers

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  • Examination of extracellular vesicles (EVs) and circulating tumor cells (CTCs) for diagnostic and prognostic applications.
  • Main Results:

    • ctDNA analysis faces challenges like low tumor fraction in differentiated thyroid cancer (DTC) but shows promise with methylation-based detection.
    • EV-miRNAs offer distinct advantages over bulk samples, with validated classifiers for metastatic disease and indeterminate nodules.
    • CTC research has evolved from enumeration to risk stratification and monitoring treatment response.

    Conclusions:

    • An indications-first framework is proposed, matching analyte choice to clinical intent (diagnosis, risk stratification, treatment response, MRD).
    • Standardization and prospective validation are crucial for clinical adoption.
    • Integration of multi-analytes, cfDNA signals (epigenetic/fragmentomic), and advanced EV analytics will accelerate clinical use, especially in advanced thyroid cancer.