Evidence map›Paper›PMID 41061668›Full record

ArticleJournal of the American Chemical Society2025

Granzyme B-Targeting Quenched Activity-Based Probes for Assessing Tumor Response to Immunotherapy.

Muhammad Kazim, Arghya Ganguly, Sebastian M Malespini, Lai Thang, Nimit L Patel, Caleb Kim, Kalyani Thakur, Joseph D Kalen, Claudia Calcagno, Simone Difilippantonio and 1 more

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2025. 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. Article
  2. Development of Granzyme A Turn-ON Fluorescent Activity-Based Probes.Chembiochem : a European journal of chemical biology · 2025
    Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Muhammad KazimChemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States.ORCID 0000-0003-2020-8952
Arghya GangulyChemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States.
Sebastian M MalespiniChemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States.
Lai ThangAnimal Research Technical Support, Laboratory of Animal Sciences Program, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland 21702, United States.
Nimit L PatelSmall Animal Imaging Program, Laboratory of Animal Sciences Program, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland 21702, United States.
Caleb KimSmall Animal Imaging Program, Laboratory of Animal Sciences Program, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland 21702, United States.
Kalyani ThakurChemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States.
Joseph D KalenSmall Animal Imaging Program, Laboratory of Animal Sciences Program, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland 21702, United States.
Claudia CalcagnoSmall Animal Imaging Program, Laboratory of Animal Sciences Program, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland 21702, United States.
Simone DifilippantonioAnimal Research Technical Support, Laboratory of Animal Sciences Program, Frederick National Laboratory for Cancer Research, National Institutes of Health, Frederick, Maryland 21702, United States.
Euna YooChemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States.ORCID 0000-0001-5982-1979

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular imaging of immune activation holds tremendous potential for the development of novel immunotherapies. In particular, chemical probes capable of detecting immune responses before changes in tumor size occur can guide early therapeutic strategies. Here, we present a quenched activity-based probe targeting granzyme B as a biomarker of antitumor immunity. Through optimization of the peptide recognition element and functional chemical warhead, we have developed an optical imaging probe, Cy5-IEPCya

Indexed as

Fluorescent DyesGranzymesImmunotherapyNeoplasmsAnimalsCarbocyaninesCell Line, TumorHumansMiceOptical ImagingCarbocyaninesFluorescent DyesGranzymes

Identifiers

PMID41061668
PMCPMC12550853

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.