Evidence map›Paper›PMID 41293692›Full record

ArticleBiomedical optics express2025

Fluorescence lifetime imaging to investigate propofol-induced metabolic alterations in MDA-MB-231 cells.

Tabassum Ahmad Tasmi, Lakhvir Singh, Alex J Walsh

Abstract read
In one paragraph

Article in Biomedical optics express, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Tabassum Ahmad TasmiDepartment of Biomedical Engineering, Texas A&M University, 3120 TAMU, College Station, TX 77843, USA.
Lakhvir SinghDepartment of Biomedical Engineering, Texas A&M University, 3120 TAMU, College Station, TX 77843, USA.
Alex J WalshDepartment of Biomedical Engineering, Texas A&M University, 3120 TAMU, College Station, TX 77843, USA.ORCID https://orcid.org/0000-0003-3832-8207

Funding

Autofluorescence lifetime microscopy for label-free detection of cell metabolism for cell biology researchR35GM142990 · NIGMS · TEXAS ENGINEERING EXPERIMENT STATION · PI Alexandra Walsh · 2021 to 2026
$2.2M
NIGMS NIH HHS R35 GM142990
6 · The paper itself

Abstract

The metabolic effects of anesthetic agents like propofol on cancer cells remain poorly understood despite the widespread use of anesthesia during cancer diagnosis and treatment. Fluorescence lifetime imaging microscopy (FLIM) was used to analyze propofol-induced metabolic changes in triple-negative breast cancer cells (MDA-MB-231) by monitoring endogenous NAD(P)H and FAD fluorescence lifetimes. FLIM of propofol-treated MDA-MB-231 cells revealed concentration-dependent shifts in metabolic states that were supported by Seahorse extracellular flux analysis. While the flux analysis provided population-averaged metabolic data, FLIM enabled high-resolution, dynamic mapping of metabolism in live cancer cells. Our study highlights FLIM as a label-free tool for investigating anesthetic-induced metabolic alterations in cells, offering insights into the potential metabolic mechanisms of propofol.

Identifiers

PMID41293692
PMCPMC12642986

What OpenQuestion holds

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Registered trials

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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.