Evidence map›Paper›PMID 28240865›Full record

ArticleACS chemical biology2017

A Near-Infrared, Wavelength-Shiftable, Turn-on Fluorescent Probe for the Detection and Imaging of Cancer Tumor Cells.

Zhenhua Shen, Bijeta Prasai, Yuko Nakamura, Hisataka Kobayashi, Milcah S Jackson, Robin L McCarley

Open access · greenAbstract read
In one paragraph

Article in ACS chemical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
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  3. Article
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  6. Recent Progress on NIR Fluorescent Probes for Enzymes.Molecules (Basel, Switzerland) · 2022
    Review
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  8. Review
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  10. Article
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  13. Review
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  17. Article
  18. Fluorescence-Guided Surgery.Frontiers in oncology · 2017
    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

6 authors at 2 institutions in 1 country.

Zhenhua ShenDepartment of Chemistry, Louisiana State University , Baton Rouge, Louisiana 70803-1804, United States.
Bijeta PrasaiDepartment of Chemistry, Louisiana State University , Baton Rouge, Louisiana 70803-1804, United States.
Yuko NakamuraMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, United States National Institutes of Health , Bethesda, Maryland 20892-1088, United States.
Hisataka KobayashiMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, United States National Institutes of Health , Bethesda, Maryland 20892-1088, United States.
Milcah S JacksonDepartment of Chemistry, Louisiana State University , Baton Rouge, Louisiana 70803-1804, United States.
Robin L McCarleyDepartment of Chemistry, Louisiana State University , Baton Rouge, Louisiana 70803-1804, United States.ORCID 0000-0002-4769-552X
Louisiana State University · USNational Institutes of Health · US

Funding

Cancer-cell specific therapy: photo-immunotherapyZIABC011513 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KOBAYASHI, HISATAKA · 2013 to 2025
$15.5M
Activatable molecular cancer imaging probeZIABC011512 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KOBAYASHI, HISATAKA · 2013 to 2025
$2.7M
Intramural NIH HHS ZIA BC011512Intramural NIH HHS ZIA BC011513
6 · The paper itself

Abstract

Fast, selective, and noninvasive reporting of intracellular cancer-associated events and species will lead to a better understanding of tumorigenesis at the molecular level and development of precision medicine approaches in oncology. Overexpressed reductase presence in solid tumor cells is key to cancer progression and protection of those diseased cells from the oxidative effects of therapeutics meant to kill them. Human NAD(P)H:quinone oxidoreductase isozyme I (hNQO1), a cytoprotective 2-electron-specific reductase found at unusually high activity levels in cancer cells of multiple origins, has attracted significant attention due to its major role in metastatic pathways and its link to low survival rates in patients, as well as its ability to effectively activate quinone-based, anticancer drugs. Accurate assessment of hNQO1 activities in living tumor models and ready differentiation of metastases from healthy tissue by fluorescent light-based protocols requires creation of hNQO1-responsive, near-infrared probes that offer deep tissue penetration and low background fluorescence. Herein, we disclose a quinone-trigger-based, near-infrared probe whose fluorescence is effectively turned on several hundred-fold through highly selective reduction of the quinone trigger group by hNQO1, with unprecedented, catalytically efficient formation of a fluorescent reporter. hNQO1 activity-specific production of a fluorescence signal in two-dimensional cultures of respiring human cancer cells that harbor the reductase enzyme allows for their quick (30 min) high-integrity recognition. The characteristics of the near-infrared probe make possible the imaging of clinically relevant three-dimensional colorectal tumor models possessing spatially heterogeneous hNQO1 activities and provide for fluorescence-assisted identification of submillimeter dimension metastases in a preclinical mouse model of human ovarian serous adenocarcinoma.

Indexed as

AnimalsCell Line, TumorDisease Models, AnimalFemaleFluorescent DyesHumansMiceNAD(P)H Dehydrogenase (Quinone)Neoplasm MetastasisOvarian NeoplasmsSpectrometry, FluorescenceSpectroscopy, Near-InfraredFluorescent DyesNAD(P)H Dehydrogenase (Quinone)NQO1 protein, human

Identifiers

PMID28240865
PMCPMC7900918
OpenAlexW2594236406

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.