Evidence map›Paper›PMID 30845739›Full record

ArticleCancers2019

Graphene Oxide-Based Targeting of Extracellular Cathepsin D and Cathepsin L As A Novel Anti-Metastatic Enzyme Cancer Therapy.

Tanveer A Tabish, Md Zahidul I Pranjol, David W Horsell, Alma A M Rahat, Jacqueline L Whatmore, Paul G Winyard, Shaowei Zhang

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  6. Review
  7. Article
  8. The Proteolytic Landscape of Ovarian Cancer: Applications in Nanomedicine.International journal of molecular sciences · 2022
    Review
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  10. Review
  11. Article
  12. Article
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  19. Article
  20. Cancer Nanomedicine.Cancers · 2020
    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

7 authors at 2 institutions in 1 country.

Tanveer A TabishCollege of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter EX4 4QF, UK. t.a.tabish2@exeter.ac.uk.
Md Zahidul I PranjolInstitute of Biomedical and Clinical Science, University of Exeter Medical School, St Luke's Campus, Exeter EX1 2LU, UK. z.pranjol@qmul.ac.uk.
David W HorsellCollege of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter EX4 4QF, UK. D.W.Horsell@exeter.ac.uk.
Alma A M RahatCollege of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter EX4 4QF, UK. A.A.M.Rahat@exeter.ac.uk.ORCID 0000-0002-5023-1371
Jacqueline L WhatmoreInstitute of Biomedical and Clinical Science, University of Exeter Medical School, St Luke's Campus, Exeter EX1 2LU, UK. j.l.whatmore@exeter.ac.uk.ORCID 0000-0002-8753-1116
Paul G WinyardInstitute of Biomedical and Clinical Science, University of Exeter Medical School, St Luke's Campus, Exeter EX1 2LU, UK. p.g.winyard@exeter.ac.uk.
Shaowei ZhangCollege of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter EX4 4QF, UK. s.zhang@exeter.ac.uk.
University of Exeter · GBQueen Mary University of London · GB

Funding

Engineering and Physical Sciences Research Council EP/L015331/1
6 · The paper itself

Abstract

Overexpression and secretion of the enzymes cathepsin D (CathD) and cathepsin L (CathL) is associated with metastasis in several human cancers. As a superfamily, extracellularly, these proteins may act within the tumor microenvironment to drive cancer progression, proliferation, invasion and metastasis. Therefore, it is important to discover novel therapeutic treatment strategies to target CathD and CathL and potentially impede metastasis. Graphene oxide (GO) could form the basis of such a strategy by acting as an adsorbent for pro-metastatic enzymes. Here, we have conducted research into the potential of targeted anti-metastatic therapy using GO to adsorb these pro-tumorigenic enzymes. Binding of CathD/L to GO revealed that CathD/L were adsorbed onto the surface of GO through its cationic and hydrophilic residues. This work could provide a roadmap for the rational integration of CathD/L-targeting agents into clinical settings.

Indexed as

adsorptionanti-metastatic enzyme cancer therapycathepsin Dcathepsin Lgraphene oxide

Identifiers

PMID30845739
PMCPMC6468385
OpenAlexW2919655648

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.