» Articles » PMID: 36213956

Urinary Cell-Free DNA in Liquid Biopsy and Cancer Management

Overview
Journal Clin Chem
Specialty Biochemistry
Date 2022 Oct 10
PMID 36213956
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The current methodology used to detect, diagnose, and monitor many types of cancers requires invasive tissue biopsy testing. Recently, liquid biopsy using blood, plasma, urine, saliva, and various other bodily fluids has shown utility to solve many issues associated with tissue biopsy. Blood/plasma has received most of the attention within the liquid biopsy field, however, obtaining blood samples from patients is still somewhat invasive and requires trained professionals. Using urine to detect cell-free DNA cancer biomarkers offers a truly non-invasive sampling method that can be easily and reproducibly conducted by patients.

Content: Novel technologies and approaches have made the detection of small quantities of cell-free tumor DNA of varying lengths possible. Recent studies using urine circulating tumor DNA to detect cancer mutations and other biomarkers have shown sensitivity comparable to blood/plasma cell-free DNA liquid biopsy for many cancer types. Thus, urine cell-free DNA liquid biopsy may replace or provide supplementary information to tissue/blood biopsies. Further investigation with larger patient cohorts and standardization of pre-analytical factors is necessary to determine the utility of urine cell-free DNA liquid biopsy for cancer detection, diagnosis, and monitoring in a clinical setting.

Summary: In this mini-review we discuss the biological aspects of cell-free DNA in urine, numerous studies using urine cell-free DNA to detect urological cancers, and recent studies using urine cell-free DNA to detect and monitor non-urological cancers including lung, breast, colorectal, and other cancers.

Citing Articles

A comprehensive overview of liquid biopsy applications in pediatric solid tumors.

Janssen F, Lak N, Janda C, Kester L, Meister M, Merks J NPJ Precis Oncol. 2024; 8(1):172.

PMID: 39097671 PMC: 11297996. DOI: 10.1038/s41698-024-00657-z.


Detection of circulatory E. granulosus-derived cell-free DNA in the plasma and urine of human cystic echinococcosis using an in-house PCR: a potential promising diagnostic biomarker.

Habibi B, Gholami S, Bagheri A, Fakhar M, Torabi M, Tabaripour R Mol Biol Rep. 2024; 51(1):452.

PMID: 38536533 DOI: 10.1007/s11033-024-09385-w.


Liquid Biopsy: An Evolving Paradigm for Non-invasive Disease Diagnosis and Monitoring in Medicine.

Adhit K, Wanjari A, Menon S, K S Cureus. 2024; 15(12):e50176.

PMID: 38192931 PMC: 10772356. DOI: 10.7759/cureus.50176.


Detection of the JAK2 V617F Mutation in Urinary Cell-free DNA in Patients with Myeloproliferative Neoplasms.

Hosoi H, Hori Y, Fukutsuka K, Osuga M, Koh Y, Mushino T Intern Med. 2023; 63(14):1987-1993.

PMID: 38008450 PMC: 11309855. DOI: 10.2169/internalmedicine.2837-23.

References
1.
Guan G, Wang Y, Sun Q, Wang L, Xie F, Yan J . Utility of urinary ctDNA to monitoring minimal residual disease in early breast cancer patients. Cancer Biomark. 2020; 28(1):111-119. DOI: 10.3233/CBM-190523. View

2.
Salvi S, Casadio V . Urinary Cell-Free DNA: Potential and Applications. Methods Mol Biol. 2018; 1909:201-209. DOI: 10.1007/978-1-4939-8973-7_15. View

3.
Saha S, Araf Y, Promon S . Circulating tumor DNA in cancer diagnosis, monitoring, and prognosis. J Egypt Natl Canc Inst. 2022; 34(1):8. DOI: 10.1186/s43046-022-00109-4. View

4.
Yao W, Mei C, Nan X, Hui L . Evaluation and comparison of in vitro degradation kinetics of DNA in serum, urine and saliva: A qualitative study. Gene. 2016; 590(1):142-8. DOI: 10.1016/j.gene.2016.06.033. View

5.
Ferrara F, Zoupanou S, Primiceri E, Ali Z, Chiriaco M . Beyond liquid biopsy: Toward non-invasive assays for distanced cancer diagnostics in pandemics. Biosens Bioelectron. 2021; 196:113698. PMC: 8527216. DOI: 10.1016/j.bios.2021.113698. View