Evidence map›Paper›PMID 35340592›Full record

ReviewBiophysical reviews2022

Urokinase plasminogen activator as an anti-metastasis target: inhibitor design principles, recent amiloride derivatives, and issues with human/mouse species selectivity.

Nehad S El Salamouni, Benjamin J Buckley, Marie Ranson, Michael J Kelso, Haibo Yu

Abstract readReview
In one paragraph

Review in Biophysical reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  3. Review
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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

5 authors.

Nehad S El SalamouniSchool of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522 Australia.
Benjamin J BuckleySchool of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522 Australia.
Marie RansonSchool of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522 Australia.
Michael J KelsoSchool of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522 Australia.
Haibo YuSchool of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522 Australia.ORCID 0000-0002-1099-2803

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The urokinase plasminogen activator (uPA) is a widely studied anticancer drug target with multiple classes of inhibitors reported to date. Many of these inhibitors contain amidine or guanidine groups, while others lacking these groups show improved oral bioavailability. Most of the X-ray co-crystal structures of small molecule uPA inhibitors show a key salt bridge with the side chain carboxylate of Asp189 in the S1 pocket of uPA. This review summarises the different classes of uPA inhibitors, their binding interactions and experimentally measured inhibitory potencies and highlights species selectivity issues with attention to recently described 6-substituted amiloride and 5‑

Indexed as

Species selectivityuPA inhibitorsUrokinase plasminogen activatorX-ray structures

Identifiers

PMID35340592
PMCPMC8921380

What OpenQuestion holds

Textmetadata
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.