Evidence map›Paper›PMID 39633886›Full record

ArticleNanophotonics (Berlin, Germany)2022

A label-free optical system with a nanohole array biosensor for discriminating live single cancer cells from normal cells.

Alfredo Franco, Verónica Vidal, Marcos Gómez, Olga Gutiérrez, María Martino, Francisco González, Fernando Moreno, José L Fernández-Luna

Abstract read
In one paragraph

Article in Nanophotonics (Berlin, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Alfredo FrancoDepartment of Applied Physics, Faculty of Sciences, University of Cantabria, Santander 39013, Spain.
Verónica VidalGenetics Unit, Valdecilla University Hospital, Santander 39008, Spain.
Marcos GómezDepartment of Surgery, Valdecilla University Hospital, Santander 39008, Spain.
Olga GutiérrezGenetics Unit, Valdecilla University Hospital, Santander 39008, Spain.
María MartinoDepartment of Pathology, Valdecilla University Hospital, Santander 39008, Spain.
Francisco GonzálezDepartment of Applied Physics, Faculty of Sciences, University of Cantabria, Santander 39013, Spain.
Fernando MorenoDepartment of Applied Physics, Faculty of Sciences, University of Cantabria, Santander 39013, Spain.
José L Fernández-LunaGenetics Unit, Valdecilla University Hospital, Santander 39008, Spain.ORCID https://orcid.org/0000-0002-1273-3338

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developing a simple, fast, and label-free method for discrimination between live cancer cells and normal cells in biological samples still remains a challenge. Here, a system is described that fulfills these features to analyze individual living cells. The system consists of a gold nanohole array biosensor plus a microscope optical design to isolate the spectral response of a single cell. It is demonstrated that differences in the spectral behavior between tumor (colorectal cancer cell lines and primary cells from colorectal cancer tissue) and non-tumor cells (peripheral blood mononuclear cells, skin fibroblasts and colon epithelial cells) are influenced by the actin cortex, which lies within the short penetration depth of the surface plasmon electromagnetic field. The efficacy of this system was assessed by the analysis of about one thousand single cells showing the highest discrimination capacity between normal colon epithelial cells and colorectal cancer cells from surgical specimens, with values of sensitivity and specificity ranging 80-100% and 87-100%, respectively. It is also demonstrated that cell discrimination capacity of the system is highly reduced by disrupting the formation of actin cortex. This plasmonic system may find wide applications in biomedicine and to study key cellular processes that involve the actin cortex, including proliferation, differentiation, and migration.

Indexed as

actin cortexcancer cellextraordinary optical transmissionplasmonics

Identifiers

PMID39633886
PMCPMC11501809

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.