Evidence map›Paper›PMID 39423271›Full record

ArticleScience advances2024

Metabolic light absorption, scattering, and emission (MetaLASE) microscopy.

Brendon S Restall, Nathaniel J M Haven, Matthew T Martell, Brendyn D Cikaluk, Joy Wang, Pradyumna Kedarisetti, Saymon Tejay, Benjamin A Adam, Gopinath Sutendra, Xingyu Li and 1 more

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

11 authors.

Brendon S RestallDepartment of Electrical and Computer Engineering, University of Alberta, 116 Street & 85 Avenue, Edmonton, Alberta T6G 2R3, Canada.ORCID 0000-0001-6410-7657
Nathaniel J M HavenDepartment of Electrical and Computer Engineering, University of Alberta, 116 Street & 85 Avenue, Edmonton, Alberta T6G 2R3, Canada.ORCID 0000-0002-1090-5503
Matthew T MartellDepartment of Electrical and Computer Engineering, University of Alberta, 116 Street & 85 Avenue, Edmonton, Alberta T6G 2R3, Canada.ORCID 0000-0001-9927-894X
Brendyn D CikalukDepartment of Electrical and Computer Engineering, University of Alberta, 116 Street & 85 Avenue, Edmonton, Alberta T6G 2R3, Canada.
Joy WangDepartment of Electrical and Computer Engineering, University of Alberta, 116 Street & 85 Avenue, Edmonton, Alberta T6G 2R3, Canada.
Pradyumna KedarisettiDepartment of Electrical and Computer Engineering, University of Alberta, 116 Street & 85 Avenue, Edmonton, Alberta T6G 2R3, Canada.ORCID 0000-0002-2522-5535
Saymon TejayDepartment of Medicine, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-0641-041X
Benjamin A AdamDepartment of Laboratory Medicine and Pathology, University of Alberta, 8440-112 Street, Edmonton, Alberta T6G 2B7, Canada.ORCID 0000-0003-1908-1739
Gopinath SutendraDepartment of Medicine, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-8181-1483
Xingyu LiDepartment of Electrical and Computer Engineering, University of Alberta, 116 Street & 85 Avenue, Edmonton, Alberta T6G 2R3, Canada.
Roger J ZempDepartment of Electrical and Computer Engineering, University of Alberta, 116 Street & 85 Avenue, Edmonton, Alberta T6G 2R3, Canada.ORCID 0000-0001-6802-5624

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Optical imaging of metabolism can provide key information about health and disease progression in cells and tissues; however, current methods have lacked gold-standard information about histological structure. Conversely, histology and virtual histology methods have lacked metabolic contrast. Here, we present metabolic light absorption, scattering, and emission (MetaLASE) microscopy, which rapidly provides a virtual histology and optical metabolic readout simultaneously. Hematoxylin-like nucleic contrast and eosin-like cytoplasmic contrast are obtained using photoacoustic remote sensing and ultraviolet reflectance microscopy, respectively. The same ultraviolet source excites endogenous Nicotinamide adenine dinucleotide (phosphate), flavin adenine dinucleotide, and collagen autofluorescence, providing a map of optical redox ratios to visualize metabolic variations including in areas of invasive carcinoma. Benign chronic inflammation and glands also are seen to exhibit hypermetabolism. MetaLASE microscopy offers promise for future applications in intraoperative margin analysis and in research applications where greater insights into metabolic activity could be correlated with cell and tissue types.

Indexed as

Optical ImagingAnimalsFlavin-Adenine DinucleotideHumansLightMicroscopyNADPScattering, RadiationFlavin-Adenine DinucleotideNADP

Identifiers

PMID39423271
PMCPMC11488571

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.