Evidence map›Paper›PMID 27626701›Full record

ArticleOncotarget2016

CDCP1 is a novel marker of the most aggressive human triple-negative breast cancers.

Federica Turdo, Francesca Bianchi, Patrizia Gasparini, Marco Sandri, Marianna Sasso, Loris De Cecco, Luca Forte, Patrizia Casalini, Piera Aiello, Lucia Sfondrini and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

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  14. 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
    Article
  15. Review
  16. TLR3 Expression Induces Apoptosis in Human Non-Small-Cell Lung Cancer.International journal of molecular sciences · 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

16 authors at 2 institutions in 1 country.

Federica TurdoMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Francesca BianchiMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Patrizia GaspariniTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Marco SandriMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Marianna SassoMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Loris De CeccoFunctional Genomic Core Facility, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Luca ForteMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Patrizia CasaliniMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Piera AielloMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Lucia SfondriniDipartimento di Scienze Biomediche per la Salute, Università degli Studi di Milano, Milan, Italy.
Roberto AgrestiDivision of Surgical Oncology, Breast Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Maria Luisa CarcangiuDivision of Breast Anatomy Pathology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Ilaria PlantamuraStart-Up Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Gabriella SozziTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Elda TagliabueMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Manuela CampiglioMolecular Targeting Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
Fondazione IRCCS Istituto Nazionale dei Tumori · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CDCP1, a transmembrane noncatalytic receptor, the expression of which has been associated with a poor prognosis in certain epithelial cancers, was found to be expressed in highly aggressive triple-negative breast cancer (TNBC) cell models, in which it promoted aggressive activities-ie, migration, invasion, anchorage-independent tumor growth, and the formation of vascular-like structures in vitro. By immunohistochemical (IHC) analysis of 100 human TNBC specimens, CDCP1 was overexpressed in 57% of samples, 38% of which exhibited a gain in CDCP1 copy number by fluorescence in situ hybridization (FISH). CDCP1 positivity was significantly associated between FISH and IHC. CDCP1 expression and gains in CDCP1 copy number synergized with nodal (N) status in determining disease-free and distant disease-free survival. The hazard ratios (HRs) of the synergies between CDCP1 positivity by IHC and FISH and lymph node positivity in predicting relapse did not differ significantly, indicating that CDCP1 overexpression in human primary TNBCs, regardless of being driven by gains in CDCP1, is for a critical factor in the progression of N-positive TNBCs. Thus, CDCP1 is a novel marker of the most aggressive N-positive TNBCs and a potential therapeutic target.

Indexed as

Antigens, CDAntigens, NeoplasmBiomarkers, TumorCell Adhesion MoleculesCell Line, TumorFemaleHumansImmunohistochemistryIn Situ Hybridization, FluorescenceNeoplasm MetastasisNeoplasm ProteinsTriple Negative Breast NeoplasmsTumor MicroenvironmentAntigens, CDAntigens, NeoplasmBiomarkers, TumorCDCP1 protein, humanCell Adhesion MoleculesNeoplasm ProteinsCDCP1CDCP1 copy numbermetastasisprognosistriple-negative breast cancer

Identifiers

PMID27626701
PMCPMC5342505
OpenAlexW2515871358

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.