» Articles » PMID: 37963993

Hydrogel-based Technologies in Liquid Biopsy for the Detection of Circulating Clinical Markers: Challenges and Prospects

Overview
Specialty Chemistry
Date 2023 Nov 14
PMID 37963993
Authors
Affiliations
Soon will be listed here.
Abstract

Liquid biopsy, which promises noninvasive detection of tumor-derived material, has recently been highlighted because of its potential to lead us to an era of precision medicine. However, its development has encountered challenges owing to the extremely low frequency and low purity of circulating tumor markers, such as circulating tumor cells (CTCs), circulating exosomes, and circulating tumor nucleic acids (ctNAs). Much effort has been made to overcome this limitation over the last decade, and an increasing number of studies have shown interest in the special characteristics of hydrogels. This hydrophilic and biocompatible polymeric network, which absorbs a large amount of water, can aid in the isolation, protection, and analysis of these low-abundance and short-lived circulating biomarkers. The role of hydrogels in liquid biopsy is extensive and ranges from enrichment to encapsulation. This review provides an overview of hydrogel-based technologies to pave the way in liquid biopsy.

Citing Articles

Polysaccharide Hydrogel-Assisted Biosensing Platforms for Point-of-Care Use.

Kim S, Kim Y, Lee T Biosensors (Basel). 2025; 15(1).

PMID: 39852065 PMC: 11763626. DOI: 10.3390/bios15010013.


Optical nanomaterial-based detection of biomarkers in liquid biopsy.

Kim Y, Rho W, Park S, Jun B J Hematol Oncol. 2024; 17(1):10.

PMID: 38486294 PMC: 10938695. DOI: 10.1186/s13045-024-01531-y.

References
1.
Speicher M, Pantel K . Tumor signatures in the blood. Nat Biotechnol. 2014; 32(5):441-3. DOI: 10.1038/nbt.2897. View

2.
Arechederra M, Avila M, Berasain C . Liquid biopsy for cancer management: a revolutionary but still limited new tool for precision medicine. Adv Lab Med. 2023; 1(3):20200009. PMC: 10197281. DOI: 10.1515/almed-2020-0009. View

3.
Gold B, Cankovic M, Furtado L, Meier F, Gocke C . Do circulating tumor cells, exosomes, and circulating tumor nucleic acids have clinical utility? A report of the association for molecular pathology. J Mol Diagn. 2015; 17(3):209-24. PMC: 4411248. DOI: 10.1016/j.jmoldx.2015.02.001. View

4.
Gerlinger M, Rowan A, Horswell S, Math M, Larkin J, Endesfelder D . Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med. 2012; 366(10):883-892. PMC: 4878653. DOI: 10.1056/NEJMoa1113205. View

5.
Longo D . Tumor heterogeneity and personalized medicine. N Engl J Med. 2012; 366(10):956-7. DOI: 10.1056/NEJMe1200656. View