Evidence map›Paper›PMID 26882065›Full record

ArticleBritish journal of cancer2016

Cell line and patient-derived xenograft models reveal elevated CDCP1 as a target in high-grade serous ovarian cancer.

Brittney S Harrington, Yaowu He, Claire M Davies, Sarah J Wallace, Mark N Adams, Elizabeth A Beaven, Deborah K Roche, Catherine Kennedy, Naven P Chetty, Alexander J Crandon and 12 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.8field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 80 citations in OpenAlex.

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  17. Theranostic Targeting of CUB Domain Containing Protein 1 (CDCP1) in Pancreatic Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
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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

22 authors at 9 institutions in 2 countries.

Brittney S HarringtonMater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Yaowu HeMater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Claire M DaviesMater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Sarah J WallaceMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
Mark N AdamsMater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Elizabeth A BeavenMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
Deborah K RocheMater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Catherine KennedyDepartment of Gynaecological Oncology, Westmead Hospital and Centre for Cancer Research, Westmead Millennium Institute, Westmead, NSW 2145, Australia.
Naven P ChettyMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
Alexander J CrandonMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
Christopher FlatleyMater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Niara B OliveiraMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
Catherine M ShannonMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
Anna deFazioDepartment of Gynaecological Oncology, Westmead Hospital and Centre for Cancer Research, Westmead Millennium Institute, Westmead, NSW 2145, Australia.
Anna V TinkerCheryl Brown Ovarian Cancer Outcomes Unit, Division of Medical Oncology and Vancouver Centre, British Columbia Cancer Agency, Vancouver, BC, Canada.
C Blake GilksDepartment of Pathology and Laboratory Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, BC, Canada.
Brian GabrielliThe University of Queensland Diamantina Institute, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Donal J BrennanMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
Jermaine I CowardMater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Jane E ArmesMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
Lewis C PerrinMater Ovarian Cancer Research Collaborative, Mater Adult Hospital, South Brisbane, QLD 4101, Australia.
John D HooperMater Research Institute, University of Queensland, Translational Research Institute, Woolloongabba, QLD 4102, Australia.
Mater Adult Hospital · AUMater Health Services · AUThe University of Queensland · AUTranslational Research Institute · AUMater Research · AUBC Cancer Agency · CAVancouver General Hospital · CAWestmead Hospital · AUWestmead Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDevelopment of targeted therapies for high-grade serous ovarian cancer (HGSC) remains challenging, as contributing molecular pathways are poorly defined or expressed heterogeneously. CUB-domain containing protein 1 (CDCP1) is a cell-surface protein elevated in lung, colorectal, pancreas, renal and clear cell ovarian cancer.

methodsCUB-domain containing protein 1 was examined by immunohistochemistry in HGSC and fallopian tube. The impact of targeting CDCP1 on cell growth and migration in vitro, and intraperitoneal xenograft growth in mice was examined. Three patient-derived xenograft (PDX) mouse models were developed and characterised for CDCP1 expression. The effect of a monoclonal anti-CDCP1 antibody on PDX growth was examined. Src activation was assessed by western blot analysis.

resultsElevated CDCP1 was observed in 77% of HGSC cases. Silencing of CDCP1 reduced migration and non-adherent cell growth in vitro and tumour burden in vivo. Expression of CDCP1 in patient samples was maintained in PDX models. Antibody blockade of CDCP1 significantly reduced growth of an HGSC PDX. The CDCP1-mediated activation of Src was observed in cultured cells and mouse xenografts.

conclusionsCUB-domain containing protein 1 is over-expressed by the majority of HGSCs. In vitro and mouse model data indicate that CDCP1 has a role in HGSC and that it can be targeted to inhibit progression of this cancer.

Indexed as

AnimalsAntigens, CDAntigens, NeoplasmBiomarkers, TumorCell Adhesion MoleculesCell Line, TumorCell MovementCell ProliferationCystadenocarcinoma, SerousDisease Models, AnimalFemaleHeterograftsHumansMiceNeoplasm GradingNeoplasm ProteinsAntigens, CDAntigens, NeoplasmBiomarkers, TumorCDCP1 protein, humanCell Adhesion MoleculesNeoplasm ProteinsRNA, Small Interfering

Identifiers

PMID26882065
PMCPMC4815773
OpenAlexW2422966071

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.