Evidence map›Paper›PMID 36942939›Full record

ArticleeLife2023

Purinergic GPCR-integrin interactions drive pancreatic cancer cell invasion.

Elena Tomas Bort, Megan D Joseph, Qiaoying Wang, Edward P Carter, Nicolas J Roth, Jessica Gibson, Ariana Samadi, Hemant M Kocher, Sabrina Simoncelli, Peter J McCormick and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. 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
3.6field-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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. 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

11 authors at 2 institutions in 1 country.

Elena Tomas BortCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0001-7897-8891
Megan D JosephLondon Centre for Nanotechnology, University College London, London, United Kingdom.ORCID 0000-0001-8313-8467
Qiaoying WangCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Edward P CarterCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0003-4499-1101
Nicolas J RothCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Jessica GibsonCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Ariana SamadiCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Hemant M KocherCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Sabrina SimoncelliLondon Centre for Nanotechnology, University College London, London, United Kingdom.ORCID 0000-0001-7089-7667
Peter J McCormickCentre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0002-2225-5181
Richard P GroseCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.ORCID 0000-0002-4738-0173
Queen Mary University of London · GBLondon Centre for Nanotechnology · GB

Funding

Biotechnology and Biological Sciences Research Council BB/T008709/1Cancer Research UK 27781Cancer Research UK A25137Cancer Research UK A27781Medical Research Council MRC0227Medical Research Council MR/N014308/1
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) continues to show no improvement in survival rates. One aspect of PDAC is elevated ATP levels, pointing to the purinergic axis as a potential attractive therapeutic target. Mediated in part by highly druggable extracellular proteins, this axis plays essential roles in fibrosis, inflammation response, and immune function. Analyzing the main members of the PDAC extracellular purinome using publicly available databases discerned which members may impact patient survival.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsAdenosine TriphosphateCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansIntegrinsNeoplasm InvasivenessReceptors, Purinergic P2Y2Adenosine TriphosphateIntegrinsP2RY2 protein, humanReceptors, Purinergic P2Y23D modellingcancer biologycell biologyDNA-PAINThumaninvasionpancreatic cancerpurinergic signalling

Identifiers

PMID36942939
PMCPMC10069867
OpenAlexW4328048525

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.