Single-molecule amplification-free multiplexed detection of circulating microRNA cancer biomarkers from serum.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
10 06 2021
Historique:
received: 13 01 2021
accepted: 30 04 2021
entrez: 11 6 2021
pubmed: 12 6 2021
medline: 30 6 2021
Statut: epublish

Résumé

MicroRNAs (miRNAs) play essential roles in post-transcriptional gene expression and are also found freely circulating in bodily fluids such as blood. Dysregulated miRNA signatures have been associated with many diseases including cancer, and miRNA profiling from liquid biopsies offers a promising strategy for cancer diagnosis, prognosis and monitoring. Here, we develop size-encoded molecular probes that can be used for simultaneous electro-optical nanopore sensing of miRNAs, allowing for ultrasensitive, sequence-specific and multiplexed detection directly in unprocessed human serum, in sample volumes as small as 0.1 μl. We show that this approach allows for femtomolar sensitivity and single-base mismatch selectivity. We demonstrate the ability to simultaneously monitor miRNAs (miR-141-3p and miR-375-3p) from prostate cancer patients with active disease and in remission. This technology can pave the way for next generation of minimally invasive diagnostic and companion diagnostic tests for cancer.

Identifiants

pubmed: 34112774
doi: 10.1038/s41467-021-23497-y
pii: 10.1038/s41467-021-23497-y
pmc: PMC8192752
doi:

Substances chimiques

Biomarkers, Tumor 0
Circulating MicroRNA 0
MIRN141 microRNA, human 0
MIRN375 microRNA, human 0
MicroRNAs 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3515

Subventions

Organisme : Cancer Research UK
ID : C49996/A26141
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/R022429/1
Pays : United Kingdom

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Auteurs

Shenglin Cai (S)

Department of Chemistry, Imperial College London, Molecular Science Research Hub, London, W12 0BZ, UK.

Thomas Pataillot-Meakin (T)

Department of Chemistry, Imperial College London, Molecular Science Research Hub, London, W12 0BZ, UK.
Department of Bioengineering, Imperial College London, Sir Michael Uren Hub, London, W12 0BZ, UK.
Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.

Akifumi Shibakawa (A)

Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.

Ren Ren (R)

Department of Chemistry, Imperial College London, Molecular Science Research Hub, London, W12 0BZ, UK.

Charlotte L Bevan (CL)

Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK. charlotte.bevan@imperial.ac.uk.

Sylvain Ladame (S)

Department of Bioengineering, Imperial College London, Sir Michael Uren Hub, London, W12 0BZ, UK. s.ladame@imperial.ac.uk.

Aleksandar P Ivanov (AP)

Department of Chemistry, Imperial College London, Molecular Science Research Hub, London, W12 0BZ, UK. alex.ivanov@imperial.ac.uk.

Joshua B Edel (JB)

Department of Chemistry, Imperial College London, Molecular Science Research Hub, London, W12 0BZ, UK. joshua.edel@imperial.ac.uk.

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Classifications MeSH