Evidence map›Paper›PMID 38951178›Full record

ArticleCommunications biology2024

Label-free morpho-molecular phenotyping of living cancer cells by combined Raman spectroscopy and phase tomography.

Arianna Bresci, Koseki J Kobayashi-Kirschvink, Giulio Cerullo, Renzo Vanna, Peter T C So, Dario Polli, Jeon Woong Kang

Abstract read
In one paragraph

Article in Communications biology, 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. Review
  2. Article
  3. 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

7 authors.

Arianna BresciG. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA. abresci@mit.edu.ORCID 0000-0003-3022-8834
Koseki J Kobayashi-KirschvinkG. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Giulio CerulloDepartment of Physics, Politecnico di Milano, Milan, 20133, Italy.ORCID 0000-0002-9534-2702
Renzo VannaCNR-Institute for Photonics and Nanotechnologies (CNR-IFN), Milan, 20133, Italy.ORCID 0000-0001-6218-8393
Peter T C SoG. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.ORCID 0000-0003-4698-6488
Dario PolliDepartment of Physics, Politecnico di Milano, Milan, 20133, Italy. dario.polli@polimi.it.ORCID 0000-0002-6960-5708
Jeon Woong KangG. R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA. jwkang76@mit.edu.ORCID 0000-0003-2012-9023

Funding

Wide-Field Short-Wave Infrared (SWIR) multiphoton (MP) tissue imagingP41EB015871 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2012 to 2021
$11.3M
Single-cell label-free identification of senescence by Raman microscopy and spatial genomicsUG3CA275687 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SO, PETER T. · 2022 to 2023
$1.1M
ROLE OF TGF B1 IN CEREBROVASCULAR AMYLOIDOSISR01AG015871 · NIA · STANFORD UNIVERSITY · PI WYSS-CORAY, TONY · 1999 to 2002
$787k
EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 101016923NCI NIH HHS UG3 CA275687NIBIB NIH HHS P41 EB015871U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) UG3CA275687U.S. Department of Health & Human Services | NIH | National Institute of Biomedical Imaging and Bioengineering (NIBIB) 5P41EB015871
6 · The paper itself

Abstract

Accurate, rapid and non-invasive cancer cell phenotyping is a pressing concern across the life sciences, as standard immuno-chemical imaging and omics require extended sample manipulation. Here we combine Raman micro-spectroscopy and phase tomography to achieve label-free morpho-molecular profiling of human colon cancer cells, following the adenoma, carcinoma, and metastasis disease progression, in living and unperturbed conditions. We describe how to decode and interpret quantitative chemical and co-registered morphological cell traits from Raman fingerprint spectra and refractive index tomograms. Our multimodal imaging strategy rapidly distinguishes cancer phenotypes, limiting observations to a low number of pristine cells in culture. This synergistic dataset allows us to study independent or correlated information in spectral and tomographic maps, and how it benefits cell type inference. This method is a valuable asset in biomedical research, particularly when biological material is in short supply, and it holds the potential for non-invasive monitoring of cancer progression in living organisms.

Indexed as

PhenotypeSpectrum Analysis, RamanCell Line, TumorColonic NeoplasmsHumans

Identifiers

PMID38951178
PMCPMC11217291

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.