Evidence map›Paper›PMID 31292126›Full record

ArticleBlood advances2019

Dual-action CXCR4-targeting liposomes in leukemia: function blocking and drug delivery.

Catriona McCallion, Anna D Peters, Andrew Booth, Karen Rees-Unwin, Julie Adams, Raisa Rahi, Alain Pluen, Claire V Hutchinson, Simon J Webb, John Burthem

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  5. Inhibition ofInternational journal of molecular sciences · 2023
    Article
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  8. Review
  9. Review
  10. Biomolecules · 2021
    Article
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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

10 authors at 5 institutions in 2 countries.

Catriona McCallionSchool of Chemistry.
Anna D PetersSchool of Chemistry.
Andrew BoothSchool of Chemistry.
Karen Rees-UnwinDivision of Cancer Sciences, School of Medical Sciences, University of Manchester, Manchester, United Kingdom.
Julie AdamsDepartment of Haematology, Manchester Royal Infirmary, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
Raisa RahiDivision of Cancer Sciences, School of Medical Sciences, University of Manchester, Manchester, United Kingdom.
Alain PluenDivision of Pharmacy and Optometry, School of Health Sciences, University of Manchester, Manchester, United Kingdom.
Claire V HutchinsonFaculty of Dentistry and Medicine, Peninsula Medical School, University of Plymouth, Plymouth, United Kingdom; and.
Simon J WebbSchool of Chemistry.ORCID 0000-0001-9793-8748
John BurthemDivision of Cancer Sciences, School of Medical Sciences, University of Manchester, Manchester, United Kingdom.
Czech Academy of Sciences, Institute of Biotechnology · CZUniversity of Manchester · GBManchester Royal Infirmary · GBManchester Academic Health Science Centre · GBUniversity Hospitals Plymouth NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CXC chemokine receptor 4 (CXCR4) is overexpressed by a broad range of hematological disorders, and its interaction with CXC chemokine ligand 12 (CXCL12) is of central importance in the retention and chemoprotection of neoplastic cells in the bone marrow and lymphoid organs. In this article, we describe the biological evaluation of a new CXCR4-targeting and -antagonizing molecule (BAT1) that we designed and show that, when incorporated into a liposomal drug delivery system, it can be used to deliver cancer therapeutics at high levels to chronic lymphocytic leukemia (CLL) cells. CXCR4 targeting and antagonism by BAT1 were demonstrated alone and following its incorporation into liposomes (BAT1-liposomes). Antagonism of BAT1 against the CXCR4/CXCL12 interaction was demonstrated through signaling inhibition and function blocking: BAT1 reduced ERK phosphorylation and cell migration to levels equivalent to those seen in the absence of CXCL12 stimulation (

Indexed as

Drug CarriersDrug Delivery SystemsLiposomesAntineoplastic AgentsCell SurvivalChemokine CXCL12DEAD-box RNA HelicasesDoxorubicinHumansLeukemiaLeukemia, Lymphocytic, Chronic, B-CellLymphocytesMolecular StructureMolecular Targeted TherapyProtein BindingReceptors, CXCR4Antineoplastic AgentsChemokine CXCL12CXCL12 protein, humanDDX39B protein, humanDEAD-box RNA HelicasesDoxorubicinDrug CarriersLiposomesReceptors, CXCR4

Identifiers

PMID31292126
PMCPMC6650733
OpenAlexW2961181283

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.