Evidence map›Paper›PMID 35501326›Full record

ArticleNature communications2022

A fluorogenic probe for granzyme B enables in-biopsy evaluation and screening of response to anticancer immunotherapies.

Jamie I Scott, Lorena Mendive-Tapia, Doireann Gordon, Nicole D Barth, Emily J Thompson, Zhiming Cheng, David Taggart, Takanori Kitamura, Alberto Bravo-Blas, Edward W Roberts and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.5field-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

27 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

22 authors at 6 institutions in 2 countries.

Jamie I ScottCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
Lorena Mendive-TapiaCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
Doireann GordonCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
Nicole D BarthCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
Emily J ThompsonCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
Zhiming ChengCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
David TaggartCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
Takanori KitamuraMRC Centre for Reproductive Health, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-2032-3918
Alberto Bravo-BlasCancer Research UK Beatson Institute, Glasgow, UK.
Edward W RobertsCancer Research UK Beatson Institute, Glasgow, UK.ORCID 0000-0002-8229-1715
Jordi Juarez-JimenezEaStChem School of Chemistry, Joseph Black Building, The University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-1464-1397
Julien MichelEaStChem School of Chemistry, Joseph Black Building, The University of Edinburgh, Edinburgh, UK.
Berber PietDepartment of Pulmonary Diseases, Radboud University Medical Centre, Nijmegen, Netherlands.ORCID 0000-0002-9069-3597
I Jolanda de VriesDepartment of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, Netherlands.ORCID 0000-0002-8653-4040
Martijn VerdoesDepartment of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, Netherlands.ORCID 0000-0001-8753-3528
John DawsonCancer Research UK Edinburgh Centre, The University of Edinburgh, Edinburgh, UK.ORCID 0000-0001-5713-1026
Neil O CarragherCancer Research UK Edinburgh Centre, The University of Edinburgh, Edinburgh, UK.
Richard A O' ConnorCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
Ahsan R AkramCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-4605-1682
Margaret FrameCancer Research UK Edinburgh Centre, The University of Edinburgh, Edinburgh, UK.
Alan SerrelsCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.ORCID 0000-0001-5882-1942
Marc VendrellCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK. marc.vendrell@ed.ac.uk.ORCID 0000-0002-5392-9740
Queen's Medical Centre · GBEdinburgh Cancer Research · GBRadboud University Nijmegen · NLCancer Research UK Scotland Institute · GBUniversity of Edinburgh · GBMRC Centre for Reproductive Health · GB

Funding

Cancer Research UK 24867Cancer Research UK 25919Cancer Research UK A24867Cancer Research UK C42454/A28596Medical Research Council MR/N022556/1Medical Research Council MR/R01566X/1Medical Research Council MR/S006982/1
6 · The paper itself

Abstract

Immunotherapy promotes the attack of cancer cells by the immune system; however, it is difficult to detect early responses before changes in tumor size occur. Here, we report the rational design of a fluorogenic peptide able to detect picomolar concentrations of active granzyme B as a biomarker of immune-mediated anticancer action. Through a series of chemical iterations and molecular dynamics simulations, we synthesize a library of FRET peptides and identify probe H5 with an optimal fit into granzyme B. We demonstrate that probe H5 enables the real-time detection of T cell-mediated anticancer activity in mouse tumors and in tumors from lung cancer patients. Furthermore, we show image-based phenotypic screens, which reveal that the AKT kinase inhibitor AZD5363 shows immune-mediated anticancer activity. The reactivity of probe H5 may enable the monitoring of early responses to anticancer treatments using tissue biopsies.

Indexed as

ImmunotherapyLung NeoplasmsAnimalsBiopsyGranzymesHumansMicePeptidesResearchGranzymesPeptides

Identifiers

PMID35501326
PMCPMC9061857
OpenAlexW4225264553

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.