Evidence map›Paper›PMID 31443478›Full record

ArticleCancers2019

Keratin-14 (KRT14) Positive Leader Cells Mediate Mesothelial Clearance and Invasion by Ovarian Cancer Cells.

Maree Bilandzic, Adam Rainczuk, Emma Green, Nicole Fairweather, Thomas W Jobling, Magdalena Plebanski, Andrew N Stephens

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 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.3field-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

39 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
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  8. Leader Cells: Invade and Evade-The Frontline of Cancer Progression.International journal of molecular sciences · 2024
    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

7 authors at 3 institutions in 1 country.

Maree BilandzicHudson Institute of Medical Research, Clayton 3168, Australia.ORCID 0000-0002-6319-1153
Adam RainczukHudson Institute of Medical Research, Clayton 3168, Australia.
Emma GreenHudson Institute of Medical Research, Clayton 3168, Australia.
Nicole FairweatherHudson Institute of Medical Research, Clayton 3168, Australia.
Thomas W JoblingDepartment of Gynaecology Oncology Monash Health, Monash Medical Centre, Moorabbin 3189, Australia.
Magdalena PlebanskiSchool of Health and Biomedical Sciences, RMIT University, Bundoora 3083, Australia.
Andrew N StephensHudson Institute of Medical Research, Clayton 3168, Australia. andrew.n.stephens@hudson.org.au.ORCID 0000-0003-2420-8458
Hudson Institute of Medical Research · AUMonash Medical Centre · AURMIT University · AU

Funding

Contributing to Australian Scholarship in Science (CASS) 001Ovarian Cancer Research Foundation (OCRF) Fellowship Dr Stephens 001Victorian Government's Operational Infrastructure Support Program 001
6 · The paper itself

Abstract

Epithelial ovarian cancer metastasis is driven by spheroids, which are heterogeneous cancer cell aggregates released from the primary tumour mass that passively disseminate throughout the peritoneal cavity to promote tumour spread, disease recurrence, and acquired chemoresistance. Despite their clinical importance, the molecular events that control spheroid attachment and invasion into underlying healthy tissues remain poorly understood. We examined a novel in vitro invasion model using imaging mass spectrometry to establish a "snapshot" of the spheroid/mesothelial interface. Amongst numerous adhesion-related proteins, we identified a sub-population of highly motile, invasive cells that expressed the basal epithelial marker KRT14 as an absolute determinant of invasive potential. The loss of KRT14 completely abrogated the invasive capacity, but had no impact on cell viability or proliferation, suggesting an invasion-specific role. Our data demonstrate KRT14 cells as an ovarian cancer "leader cell" phenotype underlying tumor invasion, and suggest their importance as a clinically relevant target in directed anti-tumour therapies.

Indexed as

cancer metastasisinvasionkeratin 14leader cellsovarian cancer

Identifiers

PMID31443478
PMCPMC6769856
OpenAlexW2969646646

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.