Evidence map›Paper›PMID 37706285›Full record

ArticleAdvanced healthcare materials2023

Multimodal Imaging of Pancreatic Cancer Microenvironment in Response to an Antiglycolytic Drug.

Elnaz Sheikh, Kirti Agrawal, Sanjit Roy, David Burk, Fabrizio Donnarumma, Young H Ko, Praveen Kumar Guttula, Nrusingh C Biswal, Hem D Shukla, Manas Ranjan Gartia

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. 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

10 authors.

Elnaz SheikhDepartment of Mechanical and Industrial Engineering, Louisiana State University, Baton Rouge, LA, 70803, USA.
Kirti AgrawalDepartment of Mechanical and Industrial Engineering, Louisiana State University, Baton Rouge, LA, 70803, USA.
Sanjit RoyDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
David BurkDepartment of Cell Biology and Bioimaging, Pennington Biomedical Research Center, Baton Rouge, LA, 70808, USA.
Fabrizio DonnarummaDepartment of Chemistry, Louisiana State University, Baton Rouge, LA, 70803, USA.
Young H KoNewG Lab Pharma, 701 East Pratt Street, Columbus Center, Baltimore, MD, 21202, USA.
Praveen Kumar GuttulaSprott Center for Stem Cell Research, Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON, K1H 8L6, Canada.
Nrusingh C BiswalDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
Hem D ShuklaDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.
Manas Ranjan GartiaDepartment of Mechanical and Industrial Engineering, Louisiana State University, Baton Rouge, LA, 70803, USA.ORCID 0000-0001-6243-6780

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI ROBERT A KESTERSON · 2005 to 2026
$26.5M
The role of maternal obesity-driven inflammation and adverse pregnancy outcomes in a mouse model of preeclampsiaP20GM135002 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Christopher D Morrison · 2020 to 2026
$18.4M
Mentoring Obesity and Diabetes Research in LouisianaP20GM103528 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2012 to 2015
$8.8M
Spatial metabolomics with subcellular resolution to identify therapeutic targetsR35GM150564 · NIGMS · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI Manas Ranjan Gartia · 2023 to 2026
$1.5M
NIDDK NIH HHS P30 DK072476NIGMS NIH HHS P20 GM103528NIGMS NIH HHS P20 GM135002NIGMS NIH HHS R35 GM150564NIH HHS P20GM103528NIH HHS P20GM135002NIH HHS P30DK072476NIH HHS R35GM150564
6 · The paper itself

Abstract

Lipid metabolism and glycolysis play crucial roles in the progression and metastasis of cancer, and the use of 3-bromopyruvate (3-BP) as an antiglycolytic agent has shown promise in killing pancreatic cancer cells. However, developing an effective strategy to avoid chemoresistance requires the ability to probe the interaction of cancer drugs with complex tumor-associated microenvironments (TAMs). Unfortunately, no robust and multiplexed molecular imaging technology is currently available to analyze TAMs. In this study, the simultaneous profiling of three protein biomarkers using SERS nanotags and antibody-functionalized nanoparticles in a syngeneic mouse model of pancreatic cancer (PC) is demonstrated. This allows for comprehensive information about biomarkers and TAM alterations before and after treatment. These multimodal imaging techniques include surface-enhanced Raman spectroscopy (SERS), immunohistochemistry (IHC), polarized light microscopy, second harmonic generation (SHG) microscopy, fluorescence lifetime imaging microscopy (FLIM), and untargeted liquid chromatography and mass spectrometry (LC-MS) analysis. The study reveals the efficacy of 3-BP in treating pancreatic cancer and identifies drug treatment-induced lipid species remodeling and associated pathways through bioinformatics analysis.

Indexed as

Pancreatic NeoplasmsTumor MicroenvironmentAnimalsBiomarkersMiceMicroscopy, FluorescenceMultimodal ImagingSpectrum Analysis, RamanBiomarkers3-bromopyruvatecancer microenvironmentglycolysislipid metabolismpancreatic cancerRaman spectroscopyWarburg effect

Identifiers

PMID37706285
PMCPMC10842640

What OpenQuestion holds

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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.