Evidence map›Paper›PMID 31330086›Full record

ReviewThe FEBS journal2019

Targeting the complexity of Src signalling in the tumour microenvironment of pancreatic cancer: from mechanism to therapy.

Ashleigh Parkin, Jennifer Man, Paul Timpson, Marina Pajic

Open access · hybridAbstract readReview
In one paragraph

Review in The FEBS journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  18. The ECM: To Scaffold, or Not to Scaffold, That Is the Question.International journal of molecular sciences · 2021
    Review
  19. 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

4 authors at 1 institution in 1 country.

Ashleigh ParkinThe Kinghorn Cancer Centre, The Garvan Institute of Medical Research, Sydney, Australia.
Jennifer ManThe Kinghorn Cancer Centre, The Garvan Institute of Medical Research, Sydney, Australia.
Paul TimpsonThe Kinghorn Cancer Centre, The Garvan Institute of Medical Research, Sydney, Australia.
Marina PajicThe Kinghorn Cancer Centre, The Garvan Institute of Medical Research, Sydney, Australia.ORCID 0000-0002-3871-3829
Garvan Institute of Medical Research · AU

Funding

Avner FoundationCancer Australia 1143699Cancer Institute NSWLen AinsworthNational Health and Medical Research Council 1162860Philip HemstritchSydney CatalystUniversity of New South Wales
6 · The paper itself

Abstract

Pancreatic cancer, a disease with extremely poor prognosis, has been notoriously resistant to virtually all forms of treatment. The dynamic crosstalk that occurs between tumour cells and the surrounding stroma, frequently mediated by intricate Src/FAK signalling, is increasingly recognised as a key player in pancreatic tumourigenesis, disease progression and therapeutic resistance. These important cues are fundamental for defining the invasive potential of pancreatic tumours, and several components of the Src and downstream effector signalling have been proposed as potent anticancer therapeutic targets. Consequently, numerous agents that block this complex network are being extensively investigated as potential antiinvasive and antimetastatic therapeutic agents for this disease. In this review, we will discuss the latest evidence of Src signalling in PDAC progression, fibrotic response and resistance to therapy. We will examine future opportunities for the development and implementation of more effective combination regimens, targeting key components of the oncogenic Src signalling axis, and in the context of a precision medicine-guided approach.

Indexed as

Molecular Targeted TherapyAntineoplastic AgentsApoptosisDrug Resistance, NeoplasmFocal Adhesion Kinase 1HumansPancreatic NeoplasmsSignal Transductionsrc-Family KinasesTumor MicroenvironmentAntineoplastic AgentsFocal Adhesion Kinase 1PTK2 protein, humansrc-Family Kinasesfocal adhesion kinaseintegrinmicroenvironmentpancreatic cancerSrc kinasestroma

Identifiers

PMID31330086
PMCPMC6771888
OpenAlexW2963005177

What Socratic 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 Socratic graph.