Evidence map›Paper›PMID 31159827›Full record

ArticleJournal of translational medicine2019

Molecular profiling of microinvasive breast cancer microenvironment progression.

F Lessi, C Scatena, P Aretini, M Menicagli, S Franceschi, A G Naccarato, C M Mazzanti

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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 2 institutions in 1 country.

F LessiGenomic Section, Fondazione Pisana per la Scienza ONLUS, via Ferruccio Giovannini, 13, S. Giuliano Terme (PI), 56017, Pisa, Italy. f.lessi@fpscience.it.ORCID 0000-0002-3346-4296
C ScatenaDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
P AretiniGenomic Section, Fondazione Pisana per la Scienza ONLUS, via Ferruccio Giovannini, 13, S. Giuliano Terme (PI), 56017, Pisa, Italy.
M MenicagliGenomic Section, Fondazione Pisana per la Scienza ONLUS, via Ferruccio Giovannini, 13, S. Giuliano Terme (PI), 56017, Pisa, Italy.
S FranceschiGenomic Section, Fondazione Pisana per la Scienza ONLUS, via Ferruccio Giovannini, 13, S. Giuliano Terme (PI), 56017, Pisa, Italy.
A G NaccaratoDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
C M MazzantiGenomic Section, Fondazione Pisana per la Scienza ONLUS, via Ferruccio Giovannini, 13, S. Giuliano Terme (PI), 56017, Pisa, Italy.
Fondazione Pisa · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumors develop by progression through a series of stages. Every cell of the tumor microenvironment is constantly changing in the flow of the cancer progression. It has become clear in recent years that stroma is essential for tumor maintenance and growth. Here, we aimed to give a chronological order of gene expression changes given in the dynamical framework of microinvasive breast cancer microenvironment.

methodsRNA-seq was performed on seven microinvasive breast cancers. For each of them we microdissected seven different portions of the tumor, four related to the breast epithelium and three to the stroma. Breast epithelium was chronologically subdivided in normal breast epithelium (NBE), carcinoma in situ (CIS), emerging invasive fingers (EIF) and invasive breast cancer (IBC). For each of the breast epithelium subdivisions we collected the adjacent stroma (S): S-NBE, S-EIF and S-IBC.

resultsThe overall differentially expressed genes (DEGs) in all the compartments were analysed and evaluated to understand the pathways involved in tumor progression. Then we analysed the DEGs of the epithelial and stromal portions in comparison with the normal portions. We observed that the stromal cells are necessary for the development and the maintenance of the tumor, especially in tumor progression. Moreover the most important genes involved in the main metabolic pathways were analysed and the communications within the different cell compartments were highlighted.

conclusionsAs a future perspective, a deeply study of the identified key genes, particularly in the stromal cells, will be crucial to develop an anticancer therapy that is undergoing a conversion from a cancer cell-centric strategy to a stroma-centric strategy, more genomically stable.

Indexed as

BreastBreast NeoplasmsCarcinoma, Intraductal, NoninfiltratingDisease ProgressionFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHigh-Throughput Nucleotide SequencingHumansMetabolic Networks and PathwaysNeoplasm InvasivenessNeoplasm StagingSequence Analysis, RNAStromal CellsTumor MicroenvironmentBreast cancerCancer microenvironmentCancer progressionLaser capture microdissectionRNA-seq

Identifiers

PMID31159827
PMCPMC6547528
OpenAlexW2948233745

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.