Evidence map›Paper›PMID 22759679›Full record

ArticleBMC research notes2012

Unmasking epithelial-mesenchymal transition in a breast cancer primary culture: a study report.

Luigi Minafra, Rossana Norata, Valentina Bravatà, Massimo Viola, Carmelo Lupo, Cecilia Gelfi, Cristina Messa

Abstract read
In one paragraph

Article in BMC research notes, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Portrait of inflammatory response to ionizing radiation treatment.Journal of inflammation (London, England) · 2015
    Article
  6. TES was epigenetically silenced and suppressed the epithelial-mesenchymal transition in breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  7. Genotyping analysis and ¹⁸FDG uptake in breast cancer patients: a preliminary research.Journal of experimental & clinical cancer research : CR · 2013
    Article
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.

Luigi MinafraInstitute of Molecular Bioimaging and Physiology (IBFM), National Council of Researches (CNR), Cefalù-Segrate, Italy. luigi.minafra@polooncologicocefalu.it
Rossana Norata
Valentina Bravatà
Massimo Viola
Carmelo Lupo
Cecilia Gelfi
Cristina Messa

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmortalized cancer cell lines are now well-established procedures in biomedicine for a more complete understanding of cellular processes in cancer. However, they are more useful in preparation of fresh tumour tissue, in order to obtain cancer cells with highly preserved individual tumour properties. In the present study we report an analytical investigation on a breast cancer primary cell culture isolated from a surgical specimen obtained from a patient with an infiltrating ductal carcinoma. The objective of the research was to reveal unrecognized aspects of neoplastic cells, typical of the tumour from where the cells were derived, but masked in fixed tissue sections, in order to better predict the aggressive potentiality of the tumour.

findingsUsing a combination of mechanical and enzymatic treatment, the tumour tissue was dissociated immediately after surgical removal. The primary cells were isolated by differential cell centrifugation and grown in selective media. Immunocytochemistry and quantitative RT-PCR analysis were performed to detect the presence of specific biomarkers at protein and transcript level.The isolated primary breast cancer cells displayed phenotypic behaviour, characteristic of malignant cells and expression of several mesenchymal markers, revealing a strong signature for the epithelial-to-mesenchymal transition associated to a stellate morphology with a number of cellular protrusions and the attitude to overgrow as multilayered overlapping cellular foci.

conclusionsOur data are a further meaningful indication that primary cell cultures represent a powerful system that could be applied to those cases deserving a deeper investigation at molecular level in order to design individualized anticancer therapies in the future.

Indexed as

Gene Expression Regulation, NeoplasticActinsBiomarkers, TumorBreast NeoplasmsCadherinsCarcinoma, Ductal, BreastCell LineEpithelial-Mesenchymal TransitionFemaleHumansImmunohistochemistryKeratinsMicroscopy, Phase-ContrastMuscle, SmoothReverse Transcriptase Polymerase Chain ReactionTumor Cells, CulturedActinsBiomarkers, TumorCadherinsKeratinsVimentin

Identifiers

PMID22759679
PMCPMC3522033

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Registered trials

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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.