Evidence map›Paper›PMID 28934230›Full record

ArticlePloS one2017

E-cadherin: A determinant molecule associated with ovarian cancer progression, dissemination and aggressiveness.

Marina Rosso, Blanca Majem, Laura Devis, Lara Lapyckyj, María José Besso, Marta Llauradó, María Florencia Abascal, María Laura Matos, Lucia Lanau, Josep Castellví and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 99 citations in OpenAlex.

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  15. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
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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

17 authors at 3 institutions in 2 countries.

Marina RossoLaboratorio de Estudios de la Interacción Celular en Reproducción y Cáncer, Instituto de Biología y Medicina Experimental (IBYME; CONICET-FIBYME), Buenos Aires, Argentina.
Blanca MajemBiomedical Research Unit in Gynecology, Vall Hebron Research Institute and University Hospital, Barcelona, Spain.
Laura DevisBiomedical Research Unit in Gynecology, Vall Hebron Research Institute and University Hospital, Barcelona, Spain.
Lara LapyckyjLaboratorio de Estudios de la Interacción Celular en Reproducción y Cáncer, Instituto de Biología y Medicina Experimental (IBYME; CONICET-FIBYME), Buenos Aires, Argentina.
María José BessoLaboratorio de Estudios de la Interacción Celular en Reproducción y Cáncer, Instituto de Biología y Medicina Experimental (IBYME; CONICET-FIBYME), Buenos Aires, Argentina.
Marta LlauradóBiomedical Research Unit in Gynecology, Vall Hebron Research Institute and University Hospital, Barcelona, Spain.
María Florencia AbascalLaboratorio de Estudios de la Interacción Celular en Reproducción y Cáncer, Instituto de Biología y Medicina Experimental (IBYME; CONICET-FIBYME), Buenos Aires, Argentina.
María Laura MatosLaboratorio de Estudios de la Interacción Celular en Reproducción y Cáncer, Instituto de Biología y Medicina Experimental (IBYME; CONICET-FIBYME), Buenos Aires, Argentina.
Lucia LanauBiomedical Research Unit in Gynecology, Vall Hebron Research Institute and University Hospital, Barcelona, Spain.
Josep CastellvíPathology Department, Vall Hebron University Hospital, Barcelona, Spain.
José Luis SánchezGynecology Oncology Department, Vall Hebron University Hospital, Barcelona, Spain.
Asunción Pérez BenaventeGynecology Oncology Department, Vall Hebron University Hospital, Barcelona, Spain.
Antonio Gil-MorenoBiomedical Research Unit in Gynecology, Vall Hebron Research Institute and University Hospital, Barcelona, Spain.
Jaume ReventósBiomedical Research Unit in Gynecology, Vall Hebron Research Institute and University Hospital, Barcelona, Spain.
Anna Santamaria MargalefBiomedical Research Unit in Gynecology, Vall Hebron Research Institute and University Hospital, Barcelona, Spain.
Marina RigauBiomedical Research Unit in Gynecology, Vall Hebron Research Institute and University Hospital, Barcelona, Spain.
Mónica Hebe Vazquez-LevinLaboratorio de Estudios de la Interacción Celular en Reproducción y Cáncer, Instituto de Biología y Medicina Experimental (IBYME; CONICET-FIBYME), Buenos Aires, Argentina.
Vall d'Hebron Institut de Recerca · ESConsejo Nacional de Investigaciones Científicas y Técnicas · ARVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer (OC) is the fifth cancer death cause in women worldwide. The malignant nature of this disease stems from its unique dissemination pattern. Epithelial-to-mesenchymal transition (EMT) has been reported in OC and downregulation of Epithelial cadherin (E-cadherin) is a hallmark of this process. However, findings on the relationship between E-cadherin levels and OC progression, dissemination and aggressiveness are controversial. In this study, the evaluation of E-cadherin expression in an OC tissue microarray revealed its prognostic value to discriminate between advanced- and early-stage tumors, as well as serous tumors from other histologies. Moreover, E-cadherin, Neural cadherin (N-cadherin), cytokeratins and vimentin expression was assessed in TOV-112, SKOV-3, OAW-42 and OV-90 OC cell lines grown in monolayers and under anchorage-independent conditions to mimic ovarian tumor cell dissemination, and results were associated with cell aggressiveness. According to these EMT-related markers, cell lines were classified as mesenchymal (M; TOV-112), intermediate mesenchymal (IM; SKOV-3), intermediate epithelial (IE; OAW-42) and epithelial (E; OV-90). M- and IM-cells depicted the highest migration capacity when grown in monolayers, and aggregates derived from M- and IM-cell lines showed lower cell death, higher adhesion to extracellular matrices and higher invasion capacity than E- and IE-aggregates. The analysis of E-cadherin, N-cadherin, cytokeratin 19 and vimentin mRNA levels in 20 advanced-stage high-grade serous human OC ascites showed an IM phenotype in all cases, characterized by higher proportions of N- to E-cadherin and vimentin to cytokeratin 19. In particular, higher E-cadherin mRNA levels were associated with cancer antigen 125 levels more than 500 U/mL and platinum-free intervals less than 6 months. Altogether, E-cadherin expression levels were found relevant for the assessment of OC progression and aggressiveness.

Indexed as

Antigens, CDAscitesBiomarkers, TumorCA-125 AntigenCadherinsCell AdhesionCell Culture TechniquesCell Line, TumorCell MovementCell SurvivalDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMembrane ProteinsNeoplasm InvasivenessAntigens, CDBiomarkers, TumorCA-125 AntigenCadherinsCDH1 protein, humanMembrane ProteinsMUC16 protein, humanRNA, Messenger

Identifiers

PMID28934230
PMCPMC5608212
OpenAlexW2757348926

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.