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Review
. 2024 Mar 14;17(1):10.
doi: 10.1186/s13045-024-01531-y.

Optical nanomaterial-based detection of biomarkers in liquid biopsy

Affiliations
Review

Optical nanomaterial-based detection of biomarkers in liquid biopsy

Young Jun Kim et al. J Hematol Oncol. .

Abstract

Liquid biopsy, which is a minimally invasive procedure as an alternative to tissue biopsy, has been introduced as a new diagnostic/prognostic measure. By screening disease-related markers from the blood or other biofluids, it promises early diagnosis, timely prognostication, and effective treatment of the diseases. However, there will be a long way until its realization due to its conceptual and practical challenges. The biomarkers detected by liquid biopsy, such as circulating tumor cell (CTC) and circulating tumor DNA (ctDNA), are extraordinarily rare and often obscured by an abundance of normal cellular components, necessitating ultra-sensitive and accurate detection methods for the advancement of liquid biopsy techniques. Optical biosensors based on nanomaterials open an important opportunity in liquid biopsy because of their enhanced sensing performance with simple and practical properties. In this review article, we summarized recent innovations in optical nanomaterials to demonstrate the sensitive detection of protein, peptide, ctDNA, miRNA, exosome, and CTCs. Each study prepares the optical nanomaterials with a tailored design to enhance the sensing performance and to meet the requirements of each biomarker. The unique optical characteristics of metallic nanoparticles (NPs), quantum dots, upconversion NPs, silica NPs, polymeric NPs, and carbon nanomaterials are exploited for sensitive detection mechanisms. These recent advances in liquid biopsy using optical nanomaterials give us an opportunity to overcome challenging issues and provide a resource for understanding the unknown characteristics of the biomarkers as well as the mechanism of the disease.

Keywords: Circulating exosomes; Circulating tumor DNAs; Circulating tumor cells; Circulating tumor markers; Liquid biopsy; Optical nanoparticles.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Biopsy and LB biomarkers: a the concept of conventional (solid) biopsy; b the concept of liquid biopsy and its advantages. c LB biomarkers and their own challenges
Fig. 2
Fig. 2
The representative optical nanomaterials and LB biomarkers. a the comparison of nanomaterials and LB biomarkers in size with scale; b illustration of AuNP-based detection of exosomes with the help of magnetic NPs; c illustration of AuNP-based detection of CTCs with the help of magnetic NPs

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References

    1. Crowley E, Di Nicolantonio F, Loupakis F, et al. Liquid biopsy: monitoring cancer-genetics in the blood. Nat Rev Clin Oncol. 2013;10:472–484. doi: 10.1038/nrclinonc.2013.110. - DOI - PubMed
    1. Alix-Panabières C, Pantel K. Real-time liquid biopsy: circulating tumor cells versus circulating tumor DNA. Ann Transl Med. 2013;1:18. - PMC - PubMed
    1. Schwarzenbach H. Circulating nucleic acids as biomarkers in breast cancer. Breast Cancer Res. 2013;15:211. doi: 10.1186/bcr3446. - DOI - PMC - PubMed
    1. Amir E, Ooi WS, Simmons C, et al. Discordance between Receptor status in primary and metastatic breast cancer: an exploratory study of bone and bone marrow biopsies. Clin Oncol. 2008;20:763–768. doi: 10.1016/j.clon.2008.08.005. - DOI - PubMed
    1. Bedard PL, Hansen AR, Ratain MJ, et al. Tumour heterogeneity in the clinic. Nature. 2013;501:355–364. doi: 10.1038/nature12627. - DOI - PMC - PubMed

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