Evidence map›Paper›PMID 36413626›Full record

ArticleJournal of the American Chemical Society2022

A KLK6 Activity-Based Probe Reveals a Role for KLK6 Activity in Pancreatic Cancer Cell Invasion.

Leran Zhang, Scott Lovell, Elena De Vita, Pravin Kumar Ankush Jagtap, Daniel Lucy, Andrea Goya Grocin, Svend Kjær, Annabel Borg, Janosch Hennig, Aubry K Miller and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Fragment-Based Discovery of KLK6 and KLK7 Inhibitors.Journal of chemical information and modeling · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Development of Granzyme A Turn-ON Fluorescent Activity-Based Probes.Chembiochem : a European journal of chemical biology · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

11 authors at 5 institutions in 2 countries.

Leran ZhangDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0002-1051-8132
Scott LovellDepartment of Life Sciences, University of Bath, Bath BA2 7AX, U.K.
Elena De VitaDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.
Pravin Kumar Ankush JagtapStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.ORCID 0000-0002-9457-4130
Daniel LucyDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.
Andrea Goya GrocinDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0002-6914-7639
Svend KjærStructural Biology Science Technology Platform, The Francis Crick Institute, London NW1 1AT, U.K.
Annabel BorgStructural Biology Science Technology Platform, The Francis Crick Institute, London NW1 1AT, U.K.
Janosch HennigStructural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.
Aubry K MillerCancer Drug Development Group, German Cancer Research Center (DKFZ), Heidelberg 69120, Germany.
Edward W TateDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0003-2213-5814
Imperial College London · GBEuropean Molecular Biology Laboratory · DEThe Francis Crick Institute · GBGerman Cancer Research Center · DEUniversity of Bath · GB

Funding

Resource for Biocomputing Visualization and InformaticsP41GM103311 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FERRIN, THOMAS E · 2012 to 2017
$8.2M
Cancer Research UK C24523/A25192Cancer Research UK C29637/A20183Cancer Research UK C29637/A21451NIGMS NIH HHS P41 GM103311
6 · The paper itself

Abstract

Pancreatic cancer has the lowest survival rate of all common cancers due to late diagnosis and limited treatment options. Serine hydrolases are known to mediate cancer progression and metastasis through initiation of signaling cascades and cleavage of extracellular matrix proteins, and the kallikrein-related peptidase (KLK) family of secreted serine proteases have emerging roles in pancreatic ductal adenocarcinoma (PDAC). However, the lack of reliable activity-based probes (ABPs) to profile KLK activity has hindered progress in validation of these enzymes as potential targets or biomarkers. Here, we developed potent and selective ABPs for KLK6 by using a positional scanning combinatorial substrate library and characterized their binding mode and interactions by X-ray crystallography. The optimized KLK6 probe IMP-2352 (

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsHumansKallikreinsNeoplasm InvasivenessKallikreinsKLK6 protein, human

Identifiers

PMID36413626
PMCPMC9756341
OpenAlexW4309650142

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.