Evidence map›Paper›PMID 37703362›Full record

ArticleScience advances2023

Noninvasive morpho-molecular imaging reveals early therapy-induced senescence in human cancer cells.

Arianna Bresci, Jeong Hee Kim, Silvia Ghislanzoni, Francesco Manetti, Lintong Wu, Federico Vernuccio, Chiara Ceconello, Salvatore Sorrentino, Ishan Barman, Italia Bongarzone and 3 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
9.3field-weighted citation impact, top 2% of its field
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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  6. Mitochondrial regulation of cellular senescence heterogeneity.Frontiers in cell and developmental biology · 2026
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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

13 authors at 4 institutions in 2 countries.

Arianna BresciDepartment of Physics, Politecnico di Milano, Milan, Italy.ORCID 0000-0003-3022-8834
Jeong Hee KimDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0001-5689-1445
Silvia GhislanzoniDepartment of Advanced Diagnostics, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.ORCID 0000-0001-5160-9885
Francesco ManettiDepartment of Physics, Politecnico di Milano, Milan, Italy.ORCID 0000-0002-8223-0074
Lintong WuDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0003-2534-0768
Federico VernuccioDepartment of Physics, Politecnico di Milano, Milan, Italy.ORCID 0000-0002-4281-7524
Chiara CeconelloDepartment of Physics, Politecnico di Milano, Milan, Italy.ORCID 0000-0003-2194-7984
Salvatore SorrentinoDepartment of Physics, Politecnico di Milano, Milan, Italy.ORCID 0000-0001-9125-5225
Ishan BarmanDepartment of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0003-0800-0825
Italia BongarzoneDepartment of Advanced Diagnostics, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.ORCID 0000-0003-2530-9170
Giulio CerulloDepartment of Physics, Politecnico di Milano, Milan, Italy.ORCID 0000-0002-9534-2702
Renzo VannaCNR-Institute for Photonics and Nanotechnologies (CNR-IFN), Milan, Italy.ORCID 0000-0001-6218-8393
Dario PolliDepartment of Physics, Politecnico di Milano, Milan, Italy.ORCID 0000-0002-6960-5708
Politecnico di Milano · ITCenter for Biomolecular Nanotechnologies · ITJohns Hopkins University · USFondazione IRCCS Istituto Nazionale dei Tumori · IT

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
Spectroscopy assisted mechano-chemical phenotype recognition nanoscopeDP2GM128198 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI BARMAN, ISHAN · 2017 to 2017
$2.5M
NIBIB NIH HHS P41 EB015871NIGMS NIH HHS DP2 GM128198
6 · The paper itself

Abstract

Anticancer therapy screening in vitro identifies additional treatments and improves clinical outcomes. Systematically, although most tested cells respond to cues with apoptosis, an appreciable portion enters a senescent state, a critical condition potentially driving tumor resistance and relapse. Conventional screening protocols would strongly benefit from prompt identification and monitoring of therapy-induced senescent (TIS) cells in their native form. We combined complementary all-optical, label-free, and quantitative microscopy techniques, based on coherent Raman scattering, multiphoton absorption, and interferometry, to explore the early onset and progression of this phenotype, which has been understudied in unperturbed conditions. We identified TIS manifestations as early as 24 hours following treatment, consisting of substantial mitochondrial rearrangement and increase of volume and dry mass, followed by accumulation of lipid vesicles starting at 72 hours. This work holds the potential to affect anticancer treatment research, by offering a label-free, rapid, and accurate method to identify initial TIS in tumor cells.

Indexed as

NeoplasmsApoptosisCuesHumansMolecular ImagingSecondary Prevention

Identifiers

PMID37703362
PMCPMC10881071
OpenAlexW4386706512

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.