Evidence map›Paper›PMID 28903399›Full record

ArticleOncotarget2017

Phosphatidylcholine-specific phospholipase C inhibition reduces HER2-overexpression, cell proliferation and

Luisa Paris, Franca Podo, Francesca Spadaro, Laura Abalsamo, Maria Elena Pisanu, Alessandro Ricci, Serena Cecchetti, Luisa Altabella, Maria Buoncervello, Ludmila Lozneanu and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Phospholipase C.Advances in experimental medicine and biology · 2020
    Review
  6. 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

16 authors at 3 institutions in 2 countries.

Luisa Paris *Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Franca Podo *Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Francesca SpadaroDepartment of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161, Roma, Italy.
Laura AbalsamoDepartment of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Maria Elena PisanuDepartment of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Alessandro RicciDepartment of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Serena CecchettiDepartment of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Luisa AltabellaDepartment of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Maria BuoncervelloDepartment of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161, Roma, Italy.
Ludmila LozneanuDepartment of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133, Milano, Italy.
Marina BagnoliDepartment of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133, Milano, Italy.
Carlo RamoniDepartment of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Silvana CanevariDepartment of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133, Milano, Italy.
Delia MezzanzanicaDepartment of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133, Milano, Italy.
Egidio Iorio *Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Rossella Canese *Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, 00161, Roma, Italy.
Istituto Superiore di Sanità · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITGrigore T. Popa University of Medicine and Pharmacy · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antagonizing the oncogenic effects of human epidermal growth factor receptor 2 (HER2) with current anti-HER2 agents has not yet yielded major progress in the treatment of advanced HER2-positive epithelial ovarian cancer (EOC). Using preclinical models to explore alternative molecular mechanisms affecting HER2 overexpression and oncogenicity may lead to new strategies for EOC patient treatment. We previously reported that phosphatidylcholine-specific phospholipase C (PC-PLC) exerts a pivotal role in regulating HER2 overexpression in breast cancer cells. The present study, conducted on two human HER2-overexpressing EOC cell lines - SKOV3 and its

Indexed as

HER2 overexpressionmagnetic resonance imagingmagnetic resonance spectroscopyovarian cancerphosphatidylcholine-specific phospholipase C

Identifiers

PMID28903399
PMCPMC5589638
OpenAlexW2729528246

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.