# Novel applications of liquid Biopsy: Comprehensive methodology for circulating biomarker exploration in peripheral blood

**Authors:** Caterina De Rosa, Luisa Amato, Annalisa Ariano, Sara Capaldo, Daniela Esposito, Hamid Heydari Sheikhhossein, Alessia Salzillo, Alessandra Di Liello, Concetta Tuccillo, Martina Cesarano, Daniela Frezzetti, Rosa Carmelingo, Antonella De Luca, Antonio Gambardella, Virginia Tirino, Fortunato Ciardiello, Floriana Morgillo, Federica Papaccio, Alberto Servetto, Viviana De Rosa, Francesca Iommelli, Carminia Maria Della Corte

PMC · DOI: 10.1016/j.jlb.2025.100307 · The Journal of Liquid Biopsy · 2025-06-26

## TL;DR

This paper presents a detailed framework for using liquid biopsy to detect cancer-related biomarkers in blood, aiming to improve early detection and treatment monitoring.

## Contribution

A comprehensive methodological framework for evaluating peripheral blood-derived biomarkers with a focus on standardization and translational application.

## Key findings

- Peripheral blood mononuclear cells, circulating tumor cells, and extracellular vesicles remain under-developed despite their potential for tumor tracking.
- Standardized protocols for liquid biopsy can help detect tumor and immune biomarkers at an early stage.
- Evaluation of circulating cytokines and PBMC dynamics in cancer patients is a promising research area.

## Abstract

The liquid biopsy (LB) represents a minimally invasive method for cancer screening that has been introduced in clinical practice for over a decade and that can accelerate treatment response assessment. LB allows the analysis of tumor cells or tumor-derived products (e.g. cell-free circulating nucleic acids, extracellular vesicles, and proteins) released from primary or metastatic tumor lesions into blood or other body fluids. In the era of immune-oncology, recent evidence indicates that tumor-specific immune responses can be detected in peripheral immune cells. The improvement of knowledge and the standardization of the isolation methods of these techniques will allow the detection and characterization of circulating tumor and immune biomarkers at an early stage as innovative tools to predict response to therapies. Nowadays, the analysis of peripheral blood mononuclear cells (PBMCs), circulating tumor cells (CTCs), peripheral blood-derived extracellular vesicles (EVs) and circulating tumor RNA (ctRNA) remains under-developed even if these non-invasive techniques can provide the complete genetic landscape of tumors and allow systematic tracking of cancer evolution. In addition, the evaluation of blood circulating cytokines, and early dynamics changes in the PBMCs of patients with solid tumors represent a promising area of research. Here, we present a comprehensive methodological framework for the evaluation of innovative peripheral blood-derived biomarkers. We also address the current challenges in isolation methods and analysis of PBMC, CTC, EVs and TEPs which are crucial for structuring the large amount of comprehensive information obtained from such samples, with the aim of advancing the translational cancer field.

Image 1

•Comprehensive detailed protocols for liquid biopsy applications.•Address the current challenges in isolation methods of circulating blood cells.•Reduces the gap due to the lack of standardized protocols.•Aims to advance the translational cancer field.

Comprehensive detailed protocols for liquid biopsy applications.

Address the current challenges in isolation methods of circulating blood cells.

Reduces the gap due to the lack of standardized protocols.

Aims to advance the translational cancer field.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Diseases:** cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12272590/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12272590/full.md

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Source: https://tomesphere.com/paper/PMC12272590