AI Article Synopsis

  • The study presents a new liquid bead array assay that detects specific mutations in circulating tumor cells (CTCs) from metastatic breast cancer (MBC) patients, which can help identify tumor progression and therapy resistance.
  • The assay utilizes advanced techniques like enzymatic mutation enrichment and multiplex PCR, allowing for highly sensitive (0.1% mutation detection limit) and specific identification of mutations in single CTCs.
  • Validation of the assay showed that it can analyze 96 single cells at once, making it both efficient and sample-conserving, thereby providing crucial insights into the genetic landscape of tumors.

Article Abstract

Background: and mutations are associated with progression and therapy resistance in metastatic breast cancer (MBC). CTCs are highly heterogeneous and their analysis at single cell level can provide unique information for mutational profiling and the existence of different sub-clones related to tumor progression. We have developed a novel multi-marker liquid bead array assay based on combination of an enzymatic mutation enrichment method, multiplex PCR-based assay, and liquid bead array technology for the simultaneous detection of and hotspot mutations in liquid biopsy samples. We focus on single CTCs, however the assay can be used for bulk CTC and ctDNA analysis.

Materials And Methods: Single CTCs were isolated from an ER+/HER2+ MBC patient from CellSearch® cartridges using the VyCAP Puncher System and subjected to whole genome amplification followed by nuclease-assisted minor-allele enrichment with probe-overlap (NaME-PrO) enrichment. The assay was validated for analytical sensitivity and specificity for the simultaneous detection of () and (Y537S) mutations in single CTCs, while its clinical performance was evaluated on 22 single CTCs and three single white blood cells (WBCs).

Results: The developed multi-marker liquid bead array assay is novel, highly specific and sensitive for both mutation panels. The assay can reliably detect mutation-allelic-frequencies (MAFs) as low as 0.1 %. The presence of and mutations was detected in 13.6 % and 72.7 % of single CTCs, respectively. The developed assay is sample-saving since it requires only 2 μL of amplified DNA to check for nine hotspot and mutations in a single cell. The developed liquid bead array assay (Luminex, US), based on a 96 microwell plate format, enables the simultaneous analysis of 96 single cells.

Conclusions: The developed novel multi-marker liquid bead array assay for the simultaneous detection of and hotspot mutations in single CTCs is highly specific, highly sensitive, high-throughput, and sample-, cost-, and time-saving. This multi-marker liquid bead array assay can be extended to detect up to 100 mutations in many genes at once and can be applied for bulk CTC and ctDNA analysis.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11462463PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e37873DOI Listing

Publication Analysis

Top Keywords

liquid bead
28
bead array
28
array assay
24
single ctcs
24
multi-marker liquid
20
simultaneous detection
16
hotspot mutations
16
mutations single
16
detection hotspot
12
assay
11

Similar Publications

Calcium alginate hydrogel is one of the most widely used materials for drug-carrier beads used in drug-delivery systems. In this study, we developed a new method to improve the encapsulation efficiency of ingredients, such as medicines, in calcium alginate hydrogel beads. In the gold standard method, the hydrogel beads are prepared in the liquid phase.

View Article and Find Full Text PDF

This study introduces an innovative bio-based sorbent bead crafted by integrating chitosan (CS) biopolymers, Fe(NO3)3 and polydopamine nanoparticles (PDA NPs) via glutaraldehyde crosslinking. The primary focus of this study was the concurrent separation of diverse tetracycline antibiotics (TCs), followed by rigorous reversed-phase liquid chromatography analysis. The fabricated CS/Fe@PDA sorbent beads were comprehensively characterized using scanning electron microscopy and energy-dispersive X-ray spectroscopy, revealing a surface rich in active carbon (C), nitrogen (N), and oxygen (O) moieties.

View Article and Find Full Text PDF

Development and thorough evaluation of a multi-omics sample preparation workflow for comprehensive LC-MS/MS-based metabolomics, lipidomics and proteomics datasets.

Talanta

December 2024

Hyphenated Mass Spectrometry Laboratory, Faculty of Science, University of Technology Sydney, PO Box 123, Broadway, 2007 NSW, Australia; School of Life Sciences, Faculty of Science, University of Technology Sydney, PO Box 123, Broadway, 2007 NSW, Australia.

The importance of sample preparation selection if often overlooked particularly for untargeted multi-omics approaches that gained popularity in recent years. To minimize issues with sample heterogeneity and additional freeze-thaw cycles during sample splitting, multiple -omics datasets (e.g.

View Article and Find Full Text PDF

Probabilistic pressure-flow operating space for chromatographic resins using mechanistic modeling.

J Chromatogr A

January 2025

Biopharm Drug Substance Development, GSK, King of Prussia, PA 19406, US.

Article Synopsis
  • Pressure drop in chromatography columns is influenced by column diameter and is challenging to predict without extensive data, but modern resin engineering has shifted focus from this issue due to larger beads.
  • Recent advancements in small-bead resins for bioprocessing have rekindled interest in understanding pressure drop, prompting the development of a mechanistic model that uses force balances to make predictions based on minimal small-scale experiments.
  • This model has been successfully tested and calibrated using different resins, allowing researchers to define safe operating ranges for pressure variables, enhancing the efficiency of resin screening before actual process development.
View Article and Find Full Text PDF

Marine microalgae are emerging as promising sources of polyphenols, renowned for their health-promoting benefits. Recovering polyphenols from microalgae requires suitable treatment and extraction techniques to ensure their release from the biomass and analytical methodologies to assess their efficiency. This review provides a comprehensive comparison of traditional and cutting-edge extraction and analytical procedures applied for polyphenolic characterization in marine microalgae over the past 26 years, with a unique perspective on optimizing their recovery and identification.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!